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Hippocampus
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<h2 id="name">Name</h2> <p>The earliest description of the ridge running along the floor of the <a href="/facts/Lateral_ventricles/gwTt9Voz">inferior horn</a> of the <a href="/facts/Lateral_ventricle/gwTt9Voz">lateral ventricle</a> comes from the Venetian anatomist <a href="/facts/Julius_Caesar_Aranzi/06eT6m9S">Julius Caesar Aranzi</a> (1587), who likened it first to a <a href="/facts/Bombyx_mori/r4IJIUtk">silkworm</a> and then to a <a href="/facts/Seahorse/fl022TMM">seahorse</a> (<a href="/facts/Latin_language/pM3Kge85">Latin</a> <i>hippocampus</i>, from <a href="/facts/Ancient_Greek/LIK7NlUh">Greek</a> ἱππόκαμπος, from ἵππος, 'horse' + κάμπος, 'sea monster').<a class="footnote-ref" id="fnref:1" href="#fn:1"><sup>1</sup></a> The German anatomist Duvernoy (1729), the first to illustrate the structure, also wavered between "seahorse" and "silkworm". "Ram's horn" was proposed by the Danish anatomist <a href="/facts/Jacob_B._Winslow/AmSwnrs5">Jacob Winsløw</a> in 1732; and a decade later his fellow Parisian, the surgeon de Garengeot, used <i>cornu Ammonis</i> – horn of <a href="/facts/Amun/e9HKGJJj">Amun</a>,<a class="footnote-ref" id="fnref:2" href="#fn:2"><sup>2</sup></a> after the ancient Egyptian god who was often represented as having a ram's head.<a class="footnote-ref" id="fnref:3" href="#fn:3"><sup>3</sup></a> <i>Ammon</i> is the Greek name for Amun.<a class="footnote-ref" id="fnref:4" href="#fn:4"><sup>4</sup></a> </p><p>The head region of the hippocampus is enlarged, and presents two or three rounded elevations or foot-like digitations, and hence it was named the pes hippocampi (<i>pes</i> meaning <i>foot</i>).<a class="footnote-ref" id="fnref:5" href="#fn:5"><sup>5</sup></a><a class="footnote-ref" id="fnref:6" href="#fn:6"><sup>6</sup></a> Later this part was described as <i>pes hippocampi major</i>, with an adjacent bulge in the <a href="/facts/Lateral_ventricles/gwTt9Voz">occipital horn of the lateral ventricle</a>, described as <i>pes hippocampi minor</i> later renamed as the <a href="/facts/Calcar_avis/Qs42TRuC">calcar avis</a>.<a class="footnote-ref" id="fnref:7" href="#fn:7"><sup>7</sup></a><a class="footnote-ref" id="fnref:8" href="#fn:8"><sup>8</sup></a> In 1786 <a href="/facts/F%C3%A9lix_Vicq-d%27Azyr/MXkTV1ty">Félix Vicq-d'Azyr</a> published an authoritative description naming just the <i>hippocampus</i> but the term remained largely unused with no description of any function proposed until in the middle of the 20th century it was associated with memory.<a class="footnote-ref" id="fnref:9" href="#fn:9"><sup>9</sup></a> </p><p><a href="/facts/Johann_Christoph_Andreas_Mayer/xLRz4XSp">Mayer</a> mistakenly used the term <a href="/facts/Hippopotamus/hFGDPWRI">hippopotamus</a> in 1779, and was followed by some other authors until <a href="/facts/Karl_Friedrich_Burdach/YFp5Nyjq">Karl Friedrich Burdach</a> resolved this error in 1829. In 1861 the hippocampus minor became the center of a dispute over <a href="/facts/Human_evolution/DNzlDyKe">human evolution</a> between <a href="/facts/Thomas_Henry_Huxley/NUNXtNdr">Thomas Henry Huxley</a> and <a href="/facts/Richard_Owen/M8H3td41">Richard Owen</a>, satirized as the <a href="/facts/Great_Hippocampus_Question/o6c5LKTJ">Great Hippocampus Question</a>. The term hippocampus minor fell from use in anatomy textbooks and was officially removed in the <a href="/facts/Nomina_Anatomica/qGuFal3o">Nomina Anatomica</a> of 1895.<a class="footnote-ref" id="fnref:10" href="#fn:10"><sup>10</sup></a> Today, the structure is just called the hippocampus, with the term <i>cornu Ammonis</i> (that is, 'Ammon's horn') surviving in the names of the <a href="/facts/Hippocampal_subfields/7zqI8mXG">hippocampal subfields</a> CA1–CA4.<a class="footnote-ref" id="fnref:11" href="#fn:11"><sup>11</sup></a><a class="footnote-ref" id="fnref:12" href="#fn:12"><sup>12</sup></a><a class="footnote-ref" id="fnref:13" href="#fn:13"><sup>13</sup></a> </p> <h2 id="in-the-limbic-system">In the limbic system</h2> <p>The hippocampus is one of the structures of the <a href="/facts/Limbic_lobe/nJu2sFz6">limbic lobe</a>, first described by <a href="/facts/Paul_Broca/Fv72wxx4">Broca</a> in 1878, as the cortical areas that line the deep edge of the cortex.<a class="footnote-ref" id="fnref:14" href="#fn:14"><sup>14</sup></a> The limbic lobe is the main component of the <a href="/facts/Limbic_system/TelEk6Jl">limbic system</a>.<a class="footnote-ref" id="fnref:15" href="#fn:15"><sup>15</sup></a> The <a href="/facts/Cingulate_gyrus/Eerbtdvr">cingulate gyrus</a>, and the <a href="/facts/Parahippocampal_gyrus/3TNGTLdG">parahippocampal gyrus</a> are the two main parts of the described lobe, which had been largely associated with <a href="/facts/Olfaction/t6ytFklU">olfaction</a>.<a class="footnote-ref" id="fnref:16" href="#fn:16"><sup>16</sup></a> Many studies later culminating in work by <a href="/facts/Papez/hwKPUqUs">Papez</a>, and <a href="/facts/Paul_D._MacLean/WEtBTor4">MacLean</a>, the involvement of other interacting brain regions associated with <a href="/facts/Emotion/kvAr22wa">emotion</a> was recognised.<a class="footnote-ref" id="fnref:17" href="#fn:17"><sup>17</sup></a> The hippocampus is anatomically connected to parts of the brain that are involved with emotional behavior, including the <a href="/facts/Septal_area/EIafRPqD">septal area</a>, the <a href="/facts/Hypothalamus/lCkNt1bM">hypothalamic</a> <a href="/facts/Mammillary_bodies/j9drXvJx">mammillary bodies</a>, and the <a href="/facts/Anterior_nuclei_of_thalamus/Fcl17P1Q">anterior nuclear complex in the thalamus</a>. MacLean proposed that the associated structures of the limbic lobe be included in what he termed as the <i>limbic system</i>.<a class="footnote-ref" id="fnref:18" href="#fn:18"><sup>18</sup></a> </p> <h2 id="anatomy">Anatomy</h2> <p class="note">See also: <a href="/facts/Hippocampus_anatomy/7zqI8mXG">Hippocampus anatomy</a></p> <p>The hippocampus is a five centimetre long ridge of <a href="/facts/Gray_matter/rqRM0qYY">gray matter tissue</a> within the <a href="/facts/Parahippocampal_gyrus/3TNGTLdG">parahippocampal gyrus</a> that can only be seen when the gyrus is opened up.<a class="footnote-ref" id="fnref:19" href="#fn:19"><sup>19</sup></a><a class="footnote-ref" id="fnref:20" href="#fn:20"><sup>20</sup></a> The hippocampus is an inward fold of three-layered <a href="/facts/Archicortex/5BNxHhpt">archicortex</a> (one of three regions of the <a href="/facts/Allocortex/gql1PsbQ">allocortex</a>) into the <a href="/facts/Temporal_lobe/U2wLVCrg">medial temporal lobe</a> of the brain, where it elevates into the floor of each <a href="/facts/Lateral_ventricle/gwTt9Voz">lateral ventricle</a> <a href="/facts/Lateral_ventricle/gwTt9Voz">inferior horn</a>.<a class="footnote-ref" id="fnref:21" href="#fn:21"><sup>21</sup></a><a class="footnote-ref" id="fnref:22" href="#fn:22"><sup>22</sup></a><a class="footnote-ref" id="fnref:23" href="#fn:23"><sup>23</sup></a><a class="footnote-ref" id="fnref:24" href="#fn:24"><sup>24</sup></a> The hippocampus stretches along its anterior-posterior axis, from the <a href="/facts/Amygdala/AAy2mHb5">amygdala</a> to the <a href="/facts/Corpus_callosum/jL54tgHn">splenium of the corpus callosum</a>, with the head, body, and tail regions as subdivisions of this axis.<a class="footnote-ref" id="fnref:25" href="#fn:25"><sup>25</sup></a><a class="footnote-ref" id="fnref:26" href="#fn:26"><sup>26</sup></a> The <a href="/facts/Dentate_gyrus/S8a0mopL">dentate gyrus</a>, CA subfields, fimbria, and <a href="/facts/Subiculum/K1NBvTBq">subiculum</a> are divisions across the short axis, the proximal-distal axis.<a class="footnote-ref" id="fnref:27" href="#fn:27"><sup>27</sup></a> </p><p>The <a href="/facts/Hippocampal_formation/WR8eRp58">hippocampal formation</a> refers to the hippocampus, and its related adjoining parts to include the dentate gyrus, the subiculum, the <a href="/facts/Presubiculum/JC26sdBK">presubiculum</a>, <a href="/facts/Parasubiculum/QrG0tTw9">parasubiculum</a>, and the <a href="/facts/Entorhinal_cortex/uRSa4Ld1">entorhinal cortex</a>.<a class="footnote-ref" id="fnref:28" href="#fn:28"><sup>28</sup></a> Sometimes the subiculum, presubiculum, and parasubiculum are grouped together as the <i>subicular complex</i>, but the regions are neuroanatomically distinct. Some sources may only include the hippocampus, dentate gyrus, and subiculum, being regions of the hippocampal three-layered archicortex.<a class="footnote-ref" id="fnref:29" href="#fn:29"><sup>29</sup></a> But the six regions are linked together serially by almost unidirectional neural pathways.<a class="footnote-ref" id="fnref:30" href="#fn:30"><sup>30</sup></a> Other sources include the <a href="/facts/Indusium_griseum/jxQ7HLmo">indusium griseum</a>, <a href="/facts/Gyrus_fasciolaris/jxQ7HLmo">gyrus fasciolaris</a>, the <a href="/facts/Medial_longitudinal_stria/Tz9gfaTl">medial</a> and <a href="/facts/Longitudinal_striae/Tz9gfaTl">longitudinal striae</a>, and <a href="/facts/Uncus/P8cyLwfa">uncus</a>, and exclude subicular regions.<a class="footnote-ref" id="fnref:31" href="#fn:31"><sup>31</sup></a><a class="footnote-ref" id="fnref:32" href="#fn:32"><sup>32</sup></a> The neural layout and pathways within the hippocampal formation are very similar in all mammals.<a class="footnote-ref" id="fnref:33" href="#fn:33"><sup>33</sup></a> </p><p>The hippocampus has a generally similar appearance across the range of mammals, from <a href="/facts/Monotreme/fLMJM4JU">egg-laying mammals</a> such as the <a href="/facts/Echidna/nhTP1K3u">echidna</a>, to humans and other <a href="/facts/Primate/Hl8RNE2X">primates</a>.<a class="footnote-ref" id="fnref:34" href="#fn:34"><sup>34</sup></a> The hippocampal-size-to-body-size ratio broadly increases, being about twice as large for primates as for the echidna. It does not, however, increase at anywhere close to the rate of the <a href="/facts/Neocortex/YEVjPgGK">neocortex</a>-to-body-size ratio. Therefore, the hippocampus takes up a much larger fraction of the cortical mantle in rodents than in primates. In adult humans the volume of the hippocampus on each side of the brain is about 3.0 to 3.5 cm3 as compared to 320 to 420 cm3 for the volume of the neocortex.<a class="footnote-ref" id="fnref:35" href="#fn:35"><sup>35</sup></a> There is also a general relationship between the size of the hippocampus and spatial memory. When comparisons are made between similar species, those that have a greater capacity for spatial memory tend to have larger hippocampal volumes.<a class="footnote-ref" id="fnref:36" href="#fn:36"><sup>36</sup></a> </p> <h2 id="neuroanatomy">Neuroanatomy</h2> <p>The hippocampus, and dentate gyrus that is folded into the hippocampal archicortex have the shape of a curved, rolled-up tube. The curve of the hippocampus (known as <i>cornu Ammonis</i>) uses the initial letters <i>CA</i> to name the <a href="/facts/Hippocampal_subfields/7zqI8mXG">hippocampal subfields CA1-CA4</a>. CA4 is in fact the polymorphic layer or <a href="/facts/Hilus/2foRWojm">hilus</a> of the dentate gyrus, but CA4 is still sometimes in use to describe the part of CA3 that inserts between the dentate gyrus regions or <i>blades</i>.<a class="footnote-ref" id="fnref:37" href="#fn:37"><sup>37</sup></a><a class="footnote-ref" id="fnref:38" href="#fn:38"><sup>38</sup></a> </p><p>It can be distinguished as an area where the cortex narrows into a single layer of densely packed <a href="/facts/Pyramidal_cell/T8MTBq8b">pyramidal neurons</a>, which curl into a tight U shape. One edge of the "U," – (CA4) the hilus of the dentate gyrus, is embedded into the backward-facing, flexed dentate gyrus. In <a href="/facts/Human/rlcTENsr">humans</a> the hippocampus is described as having an <a href="/facts/Anterior_and_posterior/IpJ1fq2f">anterior and posterior</a> part; in other primates they are termed <a href="/facts/Anatomical_terms_of_location/IpJ1fq2f">rostral and caudal</a>, and in <a href="/facts/Rodent/mT4m8QJq">rodent</a> literature they are the <a href="/facts/Anatomical_terms_of_location/IpJ1fq2f">ventral and dorsal</a> part.<a class="footnote-ref" id="fnref:39" href="#fn:39"><sup>39</sup></a> Both parts are of similar composition but belong to different <a href="/facts/Neural_circuit/pgngqMLf">neural circuits</a>.<a class="footnote-ref" id="fnref:40" href="#fn:40"><sup>40</sup></a> The dentate gyrus combined with other hippocampal regions form a banana-like structure, with the two hippocampi joined at the stems by the <a href="/facts/Fornix_(neuroanatomy)/0A8UVSjr">commissure of fornix</a> (also called the hippocampal commissure).<a class="footnote-ref" id="fnref:41" href="#fn:41"><sup>41</sup></a><a class="footnote-ref" id="fnref:42" href="#fn:42"><sup>42</sup></a> In primates, the part of the hippocampus at the bottom, near the base of the <a href="/facts/Temporal_lobe/U2wLVCrg">temporal lobe</a>, is much broader than the part at the top. This means that in cross-section the hippocampus can show a number of different shapes, depending on the angle and location of the cut.<a class="footnote-ref" id="fnref:43" href="#fn:43"><sup>43</sup></a> </p><p>In a cross-section of the hippocampus, including the dentate gyrus, several layers will be shown. The dentate gyrus has three layers of cells – the outer <i>molecular layer</i>, the middle <i>granular layer</i>, and the inner <i>polymorphic layer</i> also known as the <i>hilus</i>.<a class="footnote-ref" id="fnref:44" href="#fn:44"><sup>44</sup></a> The CA3 subfield has the following cell layers known as strata: lacunosum-moleculare, radiatum, lucidum, pyramidal, and oriens. CA2 and CA1 also have these layers except the <a href="/facts/Stratum_lucidum_of_hippocampus/LCCRvblM">lucidum stratum</a>.<a class="footnote-ref" id="fnref:45" href="#fn:45"><sup>45</sup></a> </p><p>The input to the hippocampus (from varying cortical and subcortical structures) comes from the <a href="/facts/Entorhinal_cortex/uRSa4Ld1">entorhinal cortex</a> via the <a href="/facts/Perforant_path/oMbxdKpz">perforant path</a>.<a class="footnote-ref" id="fnref:46" href="#fn:46"><sup>46</sup></a> The entorhinal cortex (EC) is strongly and reciprocally connected with many cortical and subcortical structures as well as with the brainstem. Different <a href="/facts/Thalamic_nuclei/ewXUTDKa">thalamic nuclei</a>, (from the anterior and midline groups), the <a href="/facts/Medial_septal_nucleus/IW346kv1">medial septal nucleus</a>,<a class="footnote-ref" id="fnref:47" href="#fn:47"><sup>47</sup></a> the <a href="/facts/Supramammillary_nucleus/pPWLvtDg">supramammillary nucleus</a> of the hypothalamus, and the <a href="/facts/Raphe_nuclei/DCmphm59">raphe nuclei</a> and <a href="/facts/Locus_coeruleus/tIYVuhGt">locus coeruleus</a> of the <a href="/facts/Brainstem/lD3WQbXM">brainstem</a> all send axons to the EC, so that it serves as the interface between the <a href="/facts/Neocortex/YEVjPgGK">neocortex</a> and the other connections, and the hippocampus.<a class="footnote-ref" id="fnref:48" href="#fn:48"><sup>48</sup></a> </p><p>The EC is located in the <a href="/facts/Parahippocampal_gyrus/3TNGTLdG">parahippocampal gyrus</a>, a cortical region adjacent to the hippocampus.<a class="footnote-ref" id="fnref:49" href="#fn:49"><sup>49</sup></a> This gyrus conceals the hippocampus. The parahippocampal gyrus is adjacent to the <a href="/facts/Perirhinal_cortex/asmF4Ffz">perirhinal cortex</a>, which plays an important role in the <a href="/facts/Cognitive_neuroscience_of_visual_object_recognition/xD2gBG7n">visual recognition</a> of complex objects. There is also substantial evidence that it makes a contribution to memory, which can be distinguished from the contribution of the hippocampus. It is apparent that complete <a href="/facts/Amnesia/mbHoWW9p">amnesia</a> occurs only when both the hippocampus and the parahippocampus are damaged.<a class="footnote-ref" id="fnref:50" href="#fn:50"><sup>50</sup></a> </p> <h3>Circuitry</h3> <p>The major input to the hippocampus is through the entorhinal cortex (EC), whereas its major output is via CA1 to the subiculum.<a class="footnote-ref" id="fnref:51" href="#fn:51"><sup>51</sup></a> Information reaches CA1 via two main pathways, direct and indirect. Axons from the EC that originate in layer III are the origin of the direct perforant pathway and form synapses on the very distal apical dendrites of CA1 neurons. Conversely, axons originating from layer II are the origin of the indirect pathway, and information reaches CA1 via the <a href="/facts/Trisynaptic_circuit/2gL9rJzY">trisynaptic circuit</a>. In the initial part of this pathway, the axons project through the perforant pathway to the granule cells of the dentate gyrus (first synapse). From then, the information follows via the <a href="/facts/Mossy_fiber_(hippocampus)/KMNazgfx">mossy cell fibres</a> to CA3 (second synapse). From there, CA3 axons called <a href="/facts/Schaffer_collaterals/7AFBTycT">Schaffer collaterals</a> leave the deep part of the <a href="/facts/Soma_(biology)/L8aDnXKr">cell body</a> and loop up to the apical dendrites and then extend to CA1 (third synapse).<a class="footnote-ref" id="fnref:52" href="#fn:52"><sup>52</sup></a> Axons from CA1 then project back to the entorhinal cortex, completing the circuit.<a class="footnote-ref" id="fnref:53" href="#fn:53"><sup>53</sup></a> </p><p><a href="/facts/Basket_cell/2tpEJdc8">Basket cells</a> in CA3 receive <a href="/facts/Excitatory_postsynaptic_potential/fh6J3sUm">excitatory</a> input from the pyramidal cells and then give an <a href="/facts/Inhibitory_postsynaptic_potential/Jfm13Wkn">inhibitory</a> feedback to the pyramidal cells. This <i>recurrent inhibition</i> is a simple feedback circuit that can dampen excitatory responses in the hippocampus. The pyramidal cells give a <i>recurrent excitation</i> which is an important mechanism found in some memory processing microcircuits.<a class="footnote-ref" id="fnref:54" href="#fn:54"><sup>54</sup></a> </p><p>Several other connections play important roles in hippocampal function.<a class="footnote-ref" id="fnref:55" href="#fn:55"><sup>55</sup></a> Beyond the output to the EC, additional output pathways go to other cortical areas including the <a href="/facts/Prefrontal_cortex/dypYIrwx">prefrontal cortex</a>. A major output goes via the <a href="/facts/Fornix_(neuroanatomy)/0A8UVSjr">fornix</a> to the <a href="/facts/Septal_area/EIafRPqD">lateral septal area</a> and to the <a href="/facts/Mammillary_body/j9drXvJx">mammillary body</a> of the hypothalamus (which the fornix interconnects with the hippocampus).<a class="footnote-ref" id="fnref:56" href="#fn:56"><sup>56</sup></a> The hippocampus receives modulatory input from the <a href="/facts/Serotonin/EzY58q4a">serotonin</a>, <a href="/facts/Norepinephrine/AjTIC9ox">norepinephrine</a>, and <a href="/facts/Dopamine/5gNy8Xkd">dopamine</a> systems, and from the <a href="/facts/Nucleus_reuniens/VdAAv2GX">nucleus reuniens</a> of the <a href="/facts/Thalamus/UHDtUStc">thalamus</a> to field CA1. A very important projection comes from the medial septal nucleus, which sends <a href="/facts/Cholinergic/51ttI8RK">cholinergic</a>, and <a href="/facts/Gamma_amino_butyric_acid/vRTeQQUG">gamma amino butyric acid</a> (GABA) stimulating fibers (GABAergic fibers) to all parts of the hippocampus. The inputs from the medial septal nucleus play a key role in controlling the physiological state of the hippocampus; destruction of this nucleus abolishes the hippocampal <a href="/facts/Theta_rhythm/Cmsa8j23">theta rhythm</a> and severely impairs certain types of memory.<a class="footnote-ref" id="fnref:57" href="#fn:57"><sup>57</sup></a> </p> <h3>Subfields</h3> <p><a href="/facts/Hippocampal_subfields/7zqI8mXG">Hippocampal subfields</a>, and subregions, head, body, and tail, are functionally and anatomically differentiated, and connect differently to other brain regions.<a class="footnote-ref" id="fnref:58" href="#fn:58"><sup>58</sup></a><a class="footnote-ref" id="fnref:59" href="#fn:59"><sup>59</sup></a> Their cells are morphologically different.<a class="footnote-ref" id="fnref:60" href="#fn:60"><sup>60</sup></a> They also have different levels of vulnerability to disease.<a class="footnote-ref" id="fnref:61" href="#fn:61"><sup>61</sup></a> </p><p>In humans the head of the hippocampus is termed the anterior hippocampus, the body is the intermediate hippocampus, and the tail the posterior hippocampus. The subregions all serve different functions, project with different <a href="/facts/Neural_pathway/zDpRfS6S">neural pathways</a>, and have varying numbers of <a href="/facts/Place_cell/X7FdNPD6">place cells</a>.<a class="footnote-ref" id="fnref:62" href="#fn:62"><sup>62</sup></a> (In other primates the terms used are rostral and caudal, and in rodents they are termed ventral and dorsal).<a class="footnote-ref" id="fnref:63" href="#fn:63"><sup>63</sup></a> The posterior hippocampus serves for spatial memory, verbal memory, and learning of conceptual information. Using the <a href="/facts/Radial_arm_maze/K3fkfMdL">radial arm maze</a> in rats, lesions in the dorsal hippocampus were shown to cause spatial memory impairment. Its projecting pathways include the <a href="/facts/Medial_septal_nucleus/IW346kv1">medial septal nucleus</a>, and <a href="/facts/Supramammillary_nucleus/pPWLvtDg">supramammillary nucleus</a>.<a class="footnote-ref" id="fnref:64" href="#fn:64"><sup>64</sup></a> In the rat the dorsal hippocampus also has more place cells than both the ventral and intermediate hippocampal regions.<a class="footnote-ref" id="fnref:65" href="#fn:65"><sup>65</sup></a> </p><p>In the early 20th century, the widely held view was that <a href="/facts/Olfaction/t6ytFklU">olfaction</a> was a major hippocampal function.<a class="footnote-ref" id="fnref:66" href="#fn:66"><sup>66</sup></a> This view was argued against, pointing out that the hippocampus was present in some animals such as <a href="/facts/Dolphin/NUxUP7Ph">dolphins</a> and <a href="/facts/Whale/EMJBgXfb">whales</a>, that did not have a sense of smell; and further that lesions in the temporal lobe in dogs had been shown to have no effect on their sense of smell.<a class="footnote-ref" id="fnref:67" href="#fn:67"><sup>67</sup></a> These arguments were concluded in 1947 and held for a few more decades. In 1984, and 1987, studies in the rat showed that the entorhinal cortex receives substantial input from the olfactory bulb, with part of the EC being directly innervated by the <a href="/facts/Lateral_olfactory_tract/27wTH5gI">lateral olfactory tract</a>.<a class="footnote-ref" id="fnref:68" href="#fn:68"><sup>68</sup></a> Secondary inputs to the EC were also shown to include some from the periamygdaloid and piriform cortices, and CA1 in the ventral hippocampus was shown to sends axons to the main olfactory bulb.<a class="footnote-ref" id="fnref:69" href="#fn:69"><sup>69</sup></a><a class="footnote-ref" id="fnref:70" href="#fn:70"><sup>70</sup></a> It is evident that the hippocampus does have an involvement in memory for odors.<a class="footnote-ref" id="fnref:71" href="#fn:71"><sup>71</sup></a><a class="footnote-ref" id="fnref:72" href="#fn:72"><sup>72</sup></a> </p><p>The intermediate hippocampus has overlapping characteristics with both the ventral and dorsal hippocampus.<a class="footnote-ref" id="fnref:73" href="#fn:73"><sup>73</sup></a> Studies in 2002, showed that alterations to the ventral hippocampus reduced the amount of information sent to the amygdala by the dorsal and ventral hippocampus, consequently altering fear conditioning in rats.<a class="footnote-ref" id="fnref:74" href="#fn:74"><sup>74</sup></a> In 2007, studies using <a href="/facts/Anterograde_tracing/ARPkP31W">anterograde tracing</a> methods, located the moderate projections to two primary olfactory cortical areas and prelimbic areas of the <a href="/facts/Prefrontal_cortex/dypYIrwx">medial prefrontal cortex</a>. This region has the smallest number of place cells. The ventral hippocampus functions in fear conditioning and affective processes.<a class="footnote-ref" id="fnref:75" href="#fn:75"><sup>75</sup></a> </p> <h2 id="function">Function</h2> <h3>Theories</h3> <p>Three main theories of hippocampal function have been in dominance: <a href="/facts/Inhibitory_control/XD74uhFc">response inhibition</a>, <a href="/facts/Episodic_memory/1QIEM9gQ">episodic memory</a>, and <a href="/facts/Spatial_cognition/PVdSLbwb">spatial cognition</a>. The response inhibition theory (caricatured by <a href="/facts/John_O%27Keefe_(neuroscientist)/rc1EUXEr">John O'Keefe</a> and <a href="/facts/Lynn_Nadel/UI7lcUy7">Lynn Nadel</a> as "slam on the brakes!") was very popular up to the 1960s.<a class="footnote-ref" id="fnref:76" href="#fn:76"><sup>76</sup></a> It was based largely on two observations: first, that animals with hippocampal damage tend to be <a href="/facts/Hyperactivity/uSqjIyhd">hyperactive</a>; second, that animals with hippocampal damage often have difficulty learning to inhibit previously learnt responses, especially if the response requires remaining quiet as in a <a href="/facts/Avoidance_learning/Vd6KMcgm">passive avoidance</a> test. British psychologist <a href="/facts/Jeffrey_Alan_Gray/NqKw9CJG">Jeffrey Gray</a> developed this line of thought into a complete theory of the role of the hippocampus in <a href="/facts/Anxiety/Geekl883">anxiety</a>, called the <a href="/facts/Behavioral_inhibition_system/4G0jlzdU">behavioral inhibition system</a>.<a class="footnote-ref" id="fnref:77" href="#fn:77"><sup>77</sup></a><a class="footnote-ref" id="fnref:78" href="#fn:78"><sup>78</sup></a> </p><p>The second major line of thought relates the hippocampus to memory. Although it had historical precursors, this idea derived its main impetus from a famous report by American neurosurgeon <a href="/facts/William_Beecher_Scoville/DYsvJ9q7">William Beecher Scoville</a> and British-Canadian neuropsychologist <a href="/facts/Brenda_Milner/kmCMo6q1">Brenda Milner</a>.<a class="footnote-ref" id="fnref:79" href="#fn:79"><sup>79</sup></a> It described the results of surgical destruction of the hippocampi when trying to relieve <a href="/facts/Epileptic_seizure/zuIrQyze">epileptic seizures</a> in an American man <a href="/facts/Henry_Molaison/mr9705av">Henry Molaison</a>, known until his death in 2008 as "Patient H.M."<a class="footnote-ref" id="fnref:80" href="#fn:80"><sup>80</sup></a><a class="footnote-ref" id="fnref:81" href="#fn:81"><sup>81</sup></a> The unexpected outcome of the surgery was severe <a href="/facts/Anterograde_amnesia/9peb9rmv">anterograde</a>, and partial <a href="/facts/Retrograde_amnesia/XlQbLNXd">retrograde amnesia</a>; Molaison was unable to form new <a href="/facts/Episodic_memories/1QIEM9gQ">episodic memories</a> after his surgery and could not remember any events that occurred just before his surgery, but he did retain memories of events that occurred many years earlier extending back into his childhood. This case attracted such widespread professional interest that Molaison became the most intensively studied subject in medical history.<a class="footnote-ref" id="fnref:82" href="#fn:82"><sup>82</sup></a> </p> <p>The third important theory of hippocampal function relates the hippocampus to space, and <a href="/facts/Spatial_memory/K5GuDYW3">spatial memory</a>, with the idea of a <a href="/facts/Cognitive_map/XCPtee5S">cognitive map</a> first proposed by American psychologist <a href="/facts/Edward_C._Tolman/j2T0w5X2">E.C. Tolman</a>. This theory was followed further by O'Keefe, and in 1971, he and his student Dostrovsky discovered neurons, in the rat hippocampus that seemed to show activity related to the rat's location within its environment. The neurons were described as <a href="/facts/Place_cell/X7FdNPD6">place cells</a>.<a class="footnote-ref" id="fnref:83" href="#fn:83"><sup>83</sup></a> A book was later produced in 1978, <i>The Hippocampus as a Cognitive Map</i> written by O'Keefe and Nadel.<a class="footnote-ref" id="fnref:84" href="#fn:84"><sup>84</sup></a> It has been generally agreed that the hippocampus plays a key role in spatial coding but the details are widely debated.<a class="footnote-ref" id="fnref:85" href="#fn:85"><sup>85</sup></a> </p><p>Research has focused on trying to bridge the disconnect between the two main views of hippocampal function as being split between memory and spatial cognition. In some studies, these areas have been expanded to the point of near convergence. In an attempt to reconcile the two disparate views, it is suggested that a broader view of the hippocampal function is taken and seen to have a role that encompasses both the organisation of experience (<a href="/facts/Mental_mapping/WCyqlaNh">mental mapping</a>, as per Tolman's original concept in 1948) and the directional behaviour seen as being involved in all areas of cognition, so that the function of the hippocampus can be viewed as a broader system that incorporates both the memory and the spatial perspectives in its role that involves the use of a wide scope of cognitive maps.<a class="footnote-ref" id="fnref:86" href="#fn:86"><sup>86</sup></a><a class="footnote-ref" id="fnref:87" href="#fn:87"><sup>87</sup></a><a class="footnote-ref" id="fnref:88" href="#fn:88"><sup>88</sup></a><a class="footnote-ref" id="fnref:89" href="#fn:89"><sup>89</sup></a> This relates to the <a href="/facts/Purposive_behaviorism/Y5WkRKqv">purposive behaviorism</a> born of Tolman's original goal of identifying the complex cognitive mechanisms and purposes that guided behaviour.<a class="footnote-ref" id="fnref:90" href="#fn:90"><sup>90</sup></a> </p><p>It has also been proposed that the spiking activity of hippocampal neurons is associated spatially, and it was suggested that the mechanisms of memory and planning both evolved from mechanisms of navigation and that their neuronal algorithms were basically the same.<a class="footnote-ref" id="fnref:91" href="#fn:91"><sup>91</sup></a> </p><p>Many studies have made use of <a href="/facts/Neuroimaging/dA5Cteaf">neuroimaging</a> techniques such as <a href="/facts/Functional_magnetic_resonance_imaging/GIayRTAL">functional magnetic resonance imaging</a> (fMRI), and a functional role in <a href="/facts/Approach-avoidance_conflict/qljz37qq">approach-avoidance conflict</a> has been noted. The anterior hippocampus is seen to be involved in decision-making under approach-avoidance conflict processing. It is suggested that the memory, spatial cognition, and conflict processing functions may be seen as working together and not mutually exclusive.<a class="footnote-ref" id="fnref:92" href="#fn:92"><sup>92</sup></a> </p> <h3>Role in memory</h3> <p class="note">See also: <a href="/facts/Amnesia/mbHoWW9p">Amnesia</a> and <a href="/facts/Epigenetics_in_learning_and_memory/BMKoevHv">Epigenetics in learning and memory</a></p> <p>The hippocampus is essential for the formation of <a href="/facts/Explicit_memory/vrjuSCDG">explicit memory</a>, also known as declarative memory. <a href="/facts/Episodic_memory/1QIEM9gQ">Episodic memory</a>, and <a href="/facts/Semantic_memory/NwlHHjHG">semantic memory</a> are the two components of explicit memory. <a class="footnote-ref" id="fnref:93" href="#fn:93"><sup>93</sup></a> The hippocampus also encodes emotional context from the <a href="/facts/Amygdala/AAy2mHb5">amygdala</a>. This is partly why returning to a location where an emotional event occurred may evoke that emotion. There is a deep emotional connection between episodic memories and places.<a class="footnote-ref" id="fnref:94" href="#fn:94"><sup>94</sup></a> </p><p>Due to <a href="/facts/Bilateral_symmetry/FSv5Sv4y">bilateral symmetry</a> the brain has a hippocampus in each <a href="/facts/Cerebral_hemisphere/H81aw2Qy">cerebral hemisphere</a>. If damage to the hippocampus occurs in only one hemisphere, leaving the structure intact in the other hemisphere, the brain can retain near-normal memory functioning.<a class="footnote-ref" id="fnref:95" href="#fn:95"><sup>95</sup></a> Severe damage to the hippocampi in both hemispheres results in profound difficulties in forming new memories (<a href="/facts/Anterograde_amnesia/9peb9rmv">anterograde amnesia</a>) and often also affects memories formed before the damage occurred (<a href="/facts/Retrograde_amnesia/XlQbLNXd">retrograde amnesia</a>). Although the retrograde effect normally extends many years back before the brain damage, in some cases older memories remain. This retention of older memories leads to the idea that <a href="/facts/Memory_consolidation/n9JtsvIB">consolidation</a> over time involves the transfer of memories out of the hippocampus to other parts of the brain.<a class="footnote-ref" id="fnref:96" href="#fn:96"><sup>96</sup></a>: Ch. 1 Experiments using intrahippocampal transplantation of hippocampal cells in primates with neurotoxic lesions of the hippocampus have shown that the hippocampus is required for the formation and recall, but not the storage, of memories.<a class="footnote-ref" id="fnref:97" href="#fn:97"><sup>97</sup></a> It has been shown that a decrease in the volume of various parts of the hippocampus leads to specific memory impairments. In particular, efficiency of verbal memory retention is related to the anterior parts of the right and left hippocampus. The right head of the hippocampus is more involved in executive functions and regulation during verbal memory recall. The tail of the left hippocampus tends to be closely related to verbal memory capacity.<a class="footnote-ref" id="fnref:98" href="#fn:98"><sup>98</sup></a> </p><p>Damage to the hippocampus does not affect some types of memory, such as the ability to learn new skills (playing a musical instrument or solving certain types of puzzles, for example). This fact suggests that such abilities depend on different types of memory such as <a href="/facts/Procedural_memory/3xXwEo2a">procedural memory</a> in <a href="/facts/Implicit_memory/s3FkGcTr">implicit memory</a> function, implicating different brain regions. Furthermore, amnesic patients frequently show implicit memory for experiences even in the absence of conscious knowledge. For example, patients asked to guess which of two faces they have seen most recently may give the correct answer most of the time in spite of stating that they have never seen either of the faces before. Some researchers distinguish between conscious <i>recollection</i>, which depends on the hippocampus, and <i>familiarity</i>, which depends on portions of the medial temporal lobe.<a class="footnote-ref" id="fnref:99" href="#fn:99"><sup>99</sup></a> A study claims to have confirmed that the hippocampus is not associated with implicit memory.<a class="footnote-ref" id="fnref:100" href="#fn:100"><sup>100</sup></a> But other sources say the question is still up for debate (as of 2024).<a class="footnote-ref" id="fnref:101" href="#fn:101"><sup>101</sup></a> </p><p>When rats are exposed to an intense learning event, they may retain a life-long memory of the event even after a single training session. The memory of such an event appears to be first stored in the hippocampus, but this storage is transient. Much of the long-term storage of the memory seems to take place in the <a href="/facts/Anterior_cingulate_cortex/gMBsA5EJ">anterior cingulate cortex</a>.<a class="footnote-ref" id="fnref:102" href="#fn:102"><sup>102</sup></a> When such an intense learning event was experimentally applied, more than 5,000 <a href="/facts/Differentially_methylated_region/tqCMawSL">differently methylated DNA regions</a> appeared in the hippocampus <a href="/facts/Neuron/G7CyTVdH">neuronal</a> <a href="/facts/Genome/31Sm08JT">genome</a> of the rats at one hour and at 24 hours after training.<a class="footnote-ref" id="fnref:103" href="#fn:103"><sup>103</sup></a> These alterations in <a href="/facts/DNA_methylation/npoRhsnX">methylation</a> pattern occurred at many <a href="/facts/Gene/e1swwPY6">genes</a> that were <a href="/facts/Downregulation_and_upregulation/6nRoa28r">down-regulated</a>, often due to the formation of new <a href="/facts/5-methylcytosine/mtdgxoP1">5-methylcytosine</a> sites in <a href="/facts/CpG_site/PbPHokwh">CpG rich regions</a> of the genome. Furthermore, many other genes were <a href="/facts/Downregulation_and_upregulation/6nRoa28r">upregulated</a>, likely often due to the <a href="/facts/DNA_demethylation/3UxQyVGy">removal of methyl groups</a> from previously existing <a href="/facts/5-methylcytosine/mtdgxoP1">5-methylcytosines</a> (5mCs) in DNA. Demethylation of 5mC can be carried out by several proteins acting in concert, including <a href="/facts/TET_enzymes/V5oQCJBk">TET enzymes</a><a class="footnote-ref" id="fnref:104" href="#fn:104"><sup>104</sup></a><a class="footnote-ref" id="fnref:105" href="#fn:105"><sup>105</sup></a> as well as enzymes of the DNA <a href="/facts/Base_excision_repair/QQIlyTxY">base excision repair</a> pathway.<a class="footnote-ref" id="fnref:106" href="#fn:106"><sup>106</sup></a> </p> <h4>Between systems model</h4> <p>The between-systems memory interference model describes the inhibition of non-hippocampal systems of memory during concurrent hippocampal activity.<a class="footnote-ref" id="fnref:107" href="#fn:107"><sup>107</sup></a> Specifically it was found that when the hippocampus was inactive, non-hippocampal systems located elsewhere in the brain were found to <a href="/facts/Memory_consolidation/n9JtsvIB">consolidate</a> memory in its place. However, when the hippocampus was reactivated, <a href="/facts/Engram_(neuropsychology)/m5JRMQKh">memory traces</a> consolidated by non-hippocampal systems were not recalled, suggesting that the hippocampus interferes with <a href="/facts/Long-term_memory/NvxgXP2y">long-term memory</a> consolidation in other memory-related systems.<a class="footnote-ref" id="fnref:108" href="#fn:108"><sup>108</sup></a> </p><p>One of the major implications that this model illustrates is the dominant effects of the hippocampus on non-hippocampal networks when information is incongruent. With this information in mind, future directions could lead towards the study of these non-hippocampal memory systems through hippocampal inactivation, further expanding the labile constructs of memory. Additionally, many theories of memory are holistically based around the hippocampus. This model could add beneficial information to hippocampal research and memory theories such as the <a href="/facts/Multiple_trace_theory/T2fSfkYq">multiple trace theory</a>.<a class="footnote-ref" id="fnref:109" href="#fn:109"><sup>109</sup></a><a class="footnote-ref" id="fnref:110" href="#fn:110"><sup>110</sup></a> Lastly, the between-system memory interference model allows researchers to evaluate their results on a <a href="/facts/Systems_neuroscience/ApgMwt1C">multiple-systems model</a>, suggesting that some effects may not be simply mediated by one portion of the brain.<a class="footnote-ref" id="fnref:111" href="#fn:111"><sup>111</sup></a> </p> <h3>Role in spatial memory and navigation</h3> <p class="note">Main article: <a href="/facts/Place_cell/X7FdNPD6">Place cell</a></p> <p>There are several types of <a href="/facts/Navigation/sGGAJ0AQ">navigational</a> cells in the brain that are either in the hippocampus itself or are strongly connected to it. They include the <a href="/facts/Place_cell/X7FdNPD6">place cells</a>, <a href="/facts/Speed_cells/grMMqg0v">speed cells</a> present in the <a href="/facts/Entorhinal_cortex/uRSa4Ld1">medial entorhinal cortex</a>, <a href="/facts/Head_direction_cell/pemeFQbo">head direction cells</a>, <a href="/facts/Grid_cell/tsGsogLL">grid cells</a>, and <a href="/facts/Boundary_cell/Mh9RCA2J">boundary cells</a>.<a class="footnote-ref" id="fnref:112" href="#fn:112"><sup>112</sup></a><a class="footnote-ref" id="fnref:113" href="#fn:113"><sup>113</sup></a> Together these cells form a network that serves as <a href="/facts/Spatial_memory/K5GuDYW3">spatial memory</a>. </p><p>The first of these types of cell discovered in the 1970s were the place cells, which led to the idea of the hippocampus acting to give a neural representation of the environment in a <a href="/facts/Cognitive_map/XCPtee5S">cognitive map</a>.<a class="footnote-ref" id="fnref:114" href="#fn:114"><sup>114</sup></a> When the hippocampus is dysfunctional, orientation is affected; people may have difficulty in remembering how they arrived at a location and how to proceed further. Getting lost is a common symptom of amnesia.<a class="footnote-ref" id="fnref:115" href="#fn:115"><sup>115</sup></a> Studies with animals have shown that an intact hippocampus is required for initial learning and long-term retention of some spatial memory tasks, in particular ones that require finding the way to a hidden goal.<a class="footnote-ref" id="fnref:116" href="#fn:116"><sup>116</sup></a><a class="footnote-ref" id="fnref:117" href="#fn:117"><sup>117</sup></a><a class="footnote-ref" id="fnref:118" href="#fn:118"><sup>118</sup></a><a class="footnote-ref" id="fnref:119" href="#fn:119"><sup>119</sup></a> </p><p>Studies on freely moving rats and mice have shown many hippocampal <a href="/facts/Neuron/G7CyTVdH">neurons</a> to act as <a href="/facts/Place_cell/X7FdNPD6">place cells</a> that cluster in <a href="/facts/Place_cell/X7FdNPD6">place fields</a>, and these fire bursts of <a href="/facts/Action_potential/Sz8yCRqx">action potentials</a> when the animal passes through a particular location.<a class="footnote-ref" id="fnref:120" href="#fn:120"><sup>120</sup></a> Hippocampal place cells interact extensively with head direction cells, whose activity acts as an inertial compass, and conjecturally with grid cells in the neighboring entorhinal cortex.<a class="footnote-ref" id="fnref:121" href="#fn:121"><sup>121</sup></a> Speed cells are thought to provide input to the hippocampal grid cells.<a class="footnote-ref" id="fnref:122" href="#fn:122"><sup>122</sup></a> This place-related neural activity in the hippocampus has also been reported in monkeys that were moved around a room whilst in a restraint chair.<a class="footnote-ref" id="fnref:123" href="#fn:123"><sup>123</sup></a> However, the place cells may have fired in relation to where the monkey was looking rather than to its actual location in the room.<a class="footnote-ref" id="fnref:124" href="#fn:124"><sup>124</sup></a> Over many years, many studies have been carried out on place-responses in rodents, which have given a large amount of information.<a class="footnote-ref" id="fnref:125" href="#fn:125"><sup>125</sup></a> Place cell responses are shown by <a href="/facts/Pyramidal_cell/T8MTBq8b">pyramidal cells</a> in the hippocampus and by <a href="/facts/Granule_cell/waE5b3pU">granule cells</a> in the <a href="/facts/Dentate_gyrus/S8a0mopL">dentate gyrus</a>. Other cells in smaller proportion are inhibitory <a href="/facts/Interneuron/1uca9khG">interneurons</a>, and these often show place-related variations in their firing rate that are much weaker. There is little, if any, spatial topography in the representation; in general, cells lying next to each other in the hippocampus have uncorrelated spatial <a href="/facts/Firing_pattern/knHbTaxg">firing patterns</a>. Place cells are typically almost silent when a rat is moving around outside the place field but reach sustained rates as high as 40 <a href="/facts/Hertz/6Wshj5qm">Hz</a> when the rat is near the center. Neural activity sampled from 30 to 40 randomly chosen place cells carries enough information to allow a rat's location to be reconstructed with high confidence. The size of place fields varies in a gradient along the length of the hippocampus, with cells at the dorsal end showing the smallest fields, cells near the center showing larger fields, and cells at the ventral tip showing fields that cover the entire environment.<a class="footnote-ref" id="fnref:126" href="#fn:126"><sup>126</sup></a> In some cases, the firing rate of hippocampal cells depends not only on place but also the direction a rat is moving, the destination toward which it is traveling, or other task-related variables.<a class="footnote-ref" id="fnref:127" href="#fn:127"><sup>127</sup></a> The firing of place cells is timed in relation to local theta waves, a <a href="/facts/Spatiotemporal/uRIN1x4b">spatiotemporal</a> process termed <a href="/facts/Phase_precession/Gq4VuNTF">phase precession</a>.<a class="footnote-ref" id="fnref:128" href="#fn:128"><sup>128</sup></a><a class="footnote-ref" id="fnref:129" href="#fn:129"><sup>129</sup></a> </p><p>Cells with location-specific firing patterns have been reported during a study of people with <a href="/facts/Drug-resistant_epilepsy/sMbeIzW0">drug-resistant epilepsy</a>. They were undergoing an invasive procedure to localize the source of their <a href="/facts/Seizure/zuIrQyze">seizures</a>, with a view to surgical resection. They had diagnostic electrodes implanted in their hippocampi and then used a computer to move around in a <a href="/facts/Virtual_reality/0psDGsxT">virtual reality</a> town.<a class="footnote-ref" id="fnref:130" href="#fn:130"><sup>130</sup></a> Similar <a href="/facts/Neuroimaging/dA5Cteaf">brain imaging</a> studies in <a href="/facts/Navigation/sGGAJ0AQ">navigation</a> have shown the hippocampus to be active.<a class="footnote-ref" id="fnref:131" href="#fn:131"><sup>131</sup></a> A study was carried out on taxi drivers. London's <a href="/facts/Hackney_carriage/sqWjmwsQ">black cab</a> drivers need to learn the locations of a large number of places and the fastest routes between them in order to pass a strict test known as <a href="/facts/Taxicabs_of_the_United_Kingdom/KeKt46aS">The Knowledge</a> in order to gain a license to operate. A study showed that the posterior part of the hippocampus is larger in these drivers than in the general public, and that a positive correlation exists between the length of time served as a driver and the increase in the volume of this part. It was also found the total volume of the hippocampus was unchanged, as the increase seen in the posterior part was made at the expense of the anterior part, which showed a relative decrease in size. There have been no reported adverse effects from this disparity in hippocampal proportions.<a class="footnote-ref" id="fnref:132" href="#fn:132"><sup>132</sup></a> Another study showed opposite findings in blind individuals. The anterior part of the right hippocampus was larger and the posterior part was smaller, compared with sighted individuals.<a class="footnote-ref" id="fnref:133" href="#fn:133"><sup>133</sup></a> </p> <h3>Role in approach-avoidance conflict processing</h3> <p class="note">Further information: <a href="/facts/Reward_system/fotI0rcM">Reward system</a></p> <p><a href="/facts/Approach-avoidance_conflict/qljz37qq">Approach-avoidance conflict</a> happens when a situation is presented that can either be <a href="/facts/Reward_system/fotI0rcM">rewarding</a> or punishing, and the ensuing decision-making has been associated with <a href="/facts/Anxiety/Geekl883">anxiety</a>.<a class="footnote-ref" id="fnref:134" href="#fn:134"><sup>134</sup></a> <a href="/facts/FMRI/GIayRTAL">fMRI</a> findings from studies in approach-avoidance decision-making found evidence for a functional role that is not explained by either long-term memory or spatial cognition. Overall findings showed that the anterior hippocampus is sensitive to conflict, and that it may be part of a larger cortical and subcortical network seen to be important in decision-making in uncertain conditions.<a class="footnote-ref" id="fnref:135" href="#fn:135"><sup>135</sup></a> </p><p>A review makes reference to a number of studies that show the involvement of the hippocampus in conflict tasks. The authors suggest that one challenge is to understand how conflict processing relates to the functions of spatial navigation and memory and how all of these functions need not be mutually exclusive.<a class="footnote-ref" id="fnref:136" href="#fn:136"><sup>136</sup></a> </p> <h3>Role in social memory</h3> <p class="note">Further information: <a href="/facts/Collective_memory/qcwCnmLs">Collective memory</a></p> <p>The hippocampus has received renewed attention for its role in <a href="/facts/Social_memory/qcwCnmLs">social memory</a>. Epileptic human subjects with depth electrodes in the left posterior, left anterior or right anterior hippocampus demonstrate distinct, individual cell responses when presented with faces of presumably recognizable famous people.<a class="footnote-ref" id="fnref:137" href="#fn:137"><sup>137</sup></a> Associations among facial and vocal identity were similarly mapped to the hippocampus of rheseus monkeys. Single neurons in the CA1 and CA3 responded strongly to social stimulus recognition by MRI. The CA2 was not distinguished, and may likely comprise a proportion of the claimed CA1 cells in the study.<a class="footnote-ref" id="fnref:138" href="#fn:138"><sup>138</sup></a> The dorsal CA2 and ventral CA1 subregions of the hippocampus have been implicated in social memory processing. Genetic inactivation of CA2 pyramidal neurons leads to pronounced loss of social memory, while maintaining intact sociability in mice.<a class="footnote-ref" id="fnref:139" href="#fn:139"><sup>139</sup></a> Similarly, ventral CA1 pyramidal neurons have also been demonstrated as critical for social memory under optogenetic control in mice.<a class="footnote-ref" id="fnref:140" href="#fn:140"><sup>140</sup></a><a class="footnote-ref" id="fnref:141" href="#fn:141"><sup>141</sup></a> </p> <h2 id="physiology">Physiology</h2> <p>The hippocampus shows two major modes of activity, each associated with a distinct pattern of <a href="/facts/Neural_population/6kbaP899">neural population</a> activity and waves of electrical activity as measured by an <a href="/facts/Electroencephalogram/XGvpcBl5">electroencephalogram</a> (EEG). These modes are named after the EEG patterns associated with them: <a href="/facts/Theta_waves/Cmsa8j23">theta</a> and <a href="/facts/Large_irregular_activity/9v7BrYMc">large irregular activity</a> (LIA). The main characteristics described below are for the rat, which is the animal most extensively studied.<a class="footnote-ref" id="fnref:142" href="#fn:142"><sup>142</sup></a> </p><p>The theta mode appears during states of active, alert behavior (especially locomotion), and also during <a href="/facts/Rapid_eye_movement_sleep/ySwdAgfK">REM sleep</a> (dreaming).<a class="footnote-ref" id="fnref:143" href="#fn:143"><sup>143</sup></a> In the theta mode, the EEG is dominated by large regular waves with a <a href="/facts/Frequency_range/94Rq1PkQ">frequency range</a> of 6 to 9 <a href="/facts/Hertz/6Wshj5qm">Hz</a>, and the main groups of hippocampal neurons (<a href="/facts/Pyramidal_cell/T8MTBq8b">pyramidal cells</a> and <a href="/facts/Granule_cell/waE5b3pU">granule cells</a>) show sparse population activity, which means that in any short time interval, the great majority of cells are silent, while the small remaining fraction fire at relatively high rates, up to 50 spikes in one second for the most active of them.<a class="footnote-ref" id="fnref:144" href="#fn:144"><sup>144</sup></a><a class="footnote-ref" id="fnref:145" href="#fn:145"><sup>145</sup></a> An active cell typically stays active for half a second to a few seconds. As the rat behaves, the active cells fall silent and new cells become active, but the overall percentage of active cells remains more or less constant. In many situations, cell activity is determined largely by the spatial location of the animal,<a class="footnote-ref" id="fnref:146" href="#fn:146"><sup>146</sup></a> but other behavioral variables also clearly influence it. </p><p>The LIA mode appears during <a href="/facts/Slow-wave_sleep/HIN4tW2y">slow-wave sleep</a> (non-dreaming), and also during states of waking immobility such as resting or eating.<a class="footnote-ref" id="fnref:147" href="#fn:147"><sup>147</sup></a> In the LIA mode, the EEG is dominated by sharp waves that are randomly timed large deflections of the EEG signal lasting for 25–50 milliseconds. Sharp waves are frequently generated in sets, with sets containing up to 5 or more individual sharp waves and lasting up to 500 ms. The spiking activity of neurons within the hippocampus is highly correlated with sharp wave activity. Most neurons decrease their firing rate between sharp waves; however, during a sharp wave, there is a dramatic increase in firing rate in up to 10% of the hippocampal population.<a class="footnote-ref" id="fnref:148" href="#fn:148"><sup>148</sup></a> </p><p>These two hippocampal activity modes can be seen in primates as well as rats, with the exception that it has been difficult to see robust theta rhythmicity in the primate hippocampus. There are, however, qualitatively similar sharp waves and similar state-dependent changes in neural population activity.<a class="footnote-ref" id="fnref:149" href="#fn:149"><sup>149</sup></a> </p> <h3>Hippocampal theta rhythm</h3> <p class="note">Main article: <a href="/facts/Theta_wave/Cmsa8j23">Theta wave</a></p> <p>The underlying currents producing the <a href="/facts/Theta_wave/Cmsa8j23">theta wave</a> are generated mainly by densely packed neural layers of the entorhinal cortex, CA3, and the dendrites of pyramidal cells. The theta wave is one of the largest signals seen on EEG, and is known as the hippocampal theta rhythm.<a class="footnote-ref" id="fnref:150" href="#fn:150"><sup>150</sup></a> In some situations the EEG is dominated by regular waves at 3 to 10 Hz, often continuing for many seconds. These reflect subthreshold <a href="/facts/Membrane_potential/DpNG14c7">membrane potentials</a> and strongly modulate the spiking of hippocampal neurons and synchronise across the hippocampus in a travelling wave pattern.<a class="footnote-ref" id="fnref:151" href="#fn:151"><sup>151</sup></a> The <a href="/facts/Trisynaptic_circuit/2gL9rJzY">trisynaptic circuit</a> is a relay of <a href="/facts/Neurotransmission/9H38LExu">neurotransmission</a> in the hippocampus that interacts with many brain regions. From <a href="/facts/Animal_testing_on_rodents/sck4UY6N">rodent studies</a> it has been proposed that the trisynaptic circuit generates the hippocampal theta rhythm.<a class="footnote-ref" id="fnref:152" href="#fn:152"><sup>152</sup></a> </p><p>Theta rhythmicity previously clearly shown in rabbits and rodents has also been shown in humans.<a class="footnote-ref" id="fnref:153" href="#fn:153"><sup>153</sup></a> In <a href="/facts/Laboratory_rat/3dhWomAf">rats</a> (the animals that have been the most extensively studied), theta is seen mainly in two conditions: first, when an animal is walking or in some other way actively interacting with its surroundings; second, during <a href="/facts/Rapid_eye_movement_sleep/ySwdAgfK">REM sleep</a>.<a class="footnote-ref" id="fnref:154" href="#fn:154"><sup>154</sup></a> The function of theta has not yet been convincingly explained although numerous theories have been proposed.<a class="footnote-ref" id="fnref:155" href="#fn:155"><sup>155</sup></a> The most popular hypothesis has been to relate it to learning and memory. An example would be the phase with which theta rhythms, at the time of stimulation of a neuron, shape the effect of that stimulation upon its synapses. What is meant here is that theta rhythms may affect those aspects of learning and memory that are dependent upon <a href="/facts/Synaptic_plasticity/rdVFxItN">synaptic plasticity</a>.<a class="footnote-ref" id="fnref:156" href="#fn:156"><sup>156</sup></a> It is well established that lesions of the <a href="/facts/Medial_septum/IW346kv1">medial septum</a> – the central node of the theta system – cause severe disruptions of memory.<a class="footnote-ref" id="fnref:157" href="#fn:157"><sup>157</sup></a> However, the medial septum is more than just the controller of theta; it is also the main source of <a href="/facts/Cholinergic/51ttI8RK">cholinergic</a> projections to the hippocampus.<a class="footnote-ref" id="fnref:158" href="#fn:158"><sup>158</sup></a> It has not been established that septal lesions exert their effects specifically by eliminating the theta rhythm.<a class="footnote-ref" id="fnref:159" href="#fn:159"><sup>159</sup></a> </p> <h3>Sharp waves</h3> <p class="note">Main article: <a href="/facts/Sharp_waves_and_ripples/sEXhJ8Yd">Sharp waves and ripples</a></p> <p>During sleep or during resting, when an animal is not engaged with its surroundings, the hippocampal EEG shows a pattern of irregular slow waves, somewhat larger in amplitude than theta waves. This pattern is occasionally interrupted by large surges called <i>sharp waves</i>.<a class="footnote-ref" id="fnref:160" href="#fn:160"><sup>160</sup></a> These events are associated with bursts of spike activity lasting 50 to 100 milliseconds in pyramidal cells of CA3 and CA1. They are also associated with short-lived high-frequency EEG oscillations called "ripples", with frequencies in the range 150 to 200 Hz in rats, and together they are known as <a href="/facts/Sharp_waves_and_ripples/sEXhJ8Yd">sharp waves and ripples</a>. Sharp waves are most frequent during sleep when they occur at an average rate of around 1 per second (in rats) but in a very irregular temporal pattern. Sharp waves are less frequent during inactive waking states and are usually smaller. Sharp waves have also been observed in humans and monkeys. In macaques, sharp waves are robust but do not occur as frequently as in rats.<a class="footnote-ref" id="fnref:161" href="#fn:161"><sup>161</sup></a> </p><p>Sharp waves appear to be associated with memory.<a class="footnote-ref" id="fnref:162" href="#fn:162"><sup>162</sup></a> Numerous later studies, have reported that when hippocampal place cells have overlapping spatial firing fields (and therefore often fire in near-simultaneity), they tend to show correlated activity during sleep following the behavioral session. This enhancement of correlation, commonly known as <i>reactivation</i>, has been found to occur mainly during sharp waves.<a class="footnote-ref" id="fnref:163" href="#fn:163"><sup>163</sup></a> It has been proposed that sharp waves are, in fact, reactivations of neural activity patterns that were memorized during behavior, driven by strengthening of synaptic connections within the hippocampus.<a class="footnote-ref" id="fnref:164" href="#fn:164"><sup>164</sup></a> This idea forms a key component of the "two-stage memory" theory,<a class="footnote-ref" id="fnref:165" href="#fn:165"><sup>165</sup></a> advocated by Buzsáki and others, which proposes that memories are stored within the hippocampus during behavior and then later transferred to the <a href="/facts/Neocortex/YEVjPgGK">neocortex</a> during sleep. Sharp waves in <a href="/facts/Hebbian_theory/Mmtd6Dzt">Hebbian theory</a> are seen as persistently repeated stimulations by presynaptic cells, of postsynaptic cells that are suggested to drive synaptic changes in the cortical targets of hippocampal output pathways.<a class="footnote-ref" id="fnref:166" href="#fn:166"><sup>166</sup></a> Suppression of sharp waves and ripples in sleep or during immobility can interfere with memories expressed at the level of the behavior,<a class="footnote-ref" id="fnref:167" href="#fn:167"><sup>167</sup></a><a class="footnote-ref" id="fnref:168" href="#fn:168"><sup>168</sup></a> nonetheless, the newly formed CA1 place cell code can re-emerge even after a sleep with abolished sharp waves and ripples, in spatially non-demanding tasks.<a class="footnote-ref" id="fnref:169" href="#fn:169"><sup>169</sup></a> </p> <h3>Long-term potentiation</h3> <p class="note">See also: <a href="/facts/Long-term_potentiation/AbuJmBeo">Long-term potentiation</a> and <a href="/facts/Sleep_and_learning/kl5bXHmL">Sleep and learning</a></p> <p>Since at least the time of <a href="/facts/Santiago_Ramon_y_Cajal/EUCn9yFv">Ramon y Cajal</a> (1852–1934), psychologists have speculated that the brain stores memory by altering the strength of connections between neurons that are simultaneously active.<a class="footnote-ref" id="fnref:170" href="#fn:170"><sup>170</sup></a> This idea was formalized by <a href="/facts/Donald_O._Hebb/D4a9dIuB">Donald Hebb</a> in 1949,<a class="footnote-ref" id="fnref:171" href="#fn:171"><sup>171</sup></a> but for many years remained unexplained. In 1973, <a href="/facts/Tim_Bliss/uydoESMK">Tim Bliss</a> and <a href="/facts/Terje_L%C3%B8mo/0CBdKEMV">Terje Lømo</a> described a phenomenon in the rabbit hippocampus that appeared to meet Hebb's specifications: a change in synaptic responsiveness induced by brief strong activation and lasting for hours or days or longer.<a class="footnote-ref" id="fnref:172" href="#fn:172"><sup>172</sup></a> This phenomenon was soon referred to as <a href="/facts/Long-term_potentiation/AbuJmBeo">long-term potentiation</a> (LTP). As a candidate mechanism for <a href="/facts/Long-term_memory/NvxgXP2y">long-term memory</a>, LTP has since been studied intensively, and a great deal has been learned about it. However, the complexity and variety of the intracellular signalling cascades that can trigger LTP is acknowledged as preventing a more complete understanding.<a class="footnote-ref" id="fnref:173" href="#fn:173"><sup>173</sup></a> </p><p>The hippocampus is a particularly favorable site for studying LTP because of its densely packed and sharply defined layers of neurons, but similar types of activity-dependent synaptic change have also been observed in many other brain areas.<a class="footnote-ref" id="fnref:174" href="#fn:174"><sup>174</sup></a> The best-studied form of LTP has been seen in CA1 of the hippocampus and occurs at synapses that terminate on <a href="/facts/Dendritic_spine/wg54o3YT">dendritic spines</a> and use the <a href="/facts/Neurotransmitter/LlpYFSU3">neurotransmitter</a> <a href="/facts/Glutamate/7oXbNcvu">glutamate</a>.<a class="footnote-ref" id="fnref:175" href="#fn:175"><sup>175</sup></a> The synaptic changes depend on a special type of <a href="/facts/Glutamate_receptor/MGwpHHUA">glutamate receptor</a>, the <a href="/facts/NMDA_receptor/BqMhXEbU"><i>N</i>-methyl-D-aspartate (NMDA) receptor</a>, a <a href="/facts/Cell_surface_receptor/0YGSjDdL">cell surface receptor</a> which has the special property of allowing calcium to enter the postsynaptic spine only when presynaptic activation and postsynaptic <a href="/facts/Depolarization/qGX8lFXE">depolarization</a> occur at the same time.<a class="footnote-ref" id="fnref:176" href="#fn:176"><sup>176</sup></a> Drugs that interfere with NMDA receptors block LTP and have major effects on some types of memory, especially spatial memory. <a href="/facts/Genetically_modified_mouse/cGycqMQ2">Genetically modified mice</a> that are <a href="/facts/Genetic_engineering/vwdlDR61">modified</a> to disable the LTP mechanism, also generally show severe memory deficits.<a class="footnote-ref" id="fnref:177" href="#fn:177"><sup>177</sup></a> </p> <h2 id="research">Research</h2> <p>A <a href="/facts/Brain_implant/eaHAKydz">brain implant</a> as a <a href="/facts/Hippocampal_prosthesis/0QSHfWNI">hippocampal prosthesis</a> is a focus of research. As of 2025, further trials of a memory in–memory out (MIMO) model that has been developed, are ongoing. The MIMO model has been shown in some studies to restore and improve memory function.<a class="footnote-ref" id="fnref:178" href="#fn:178"><sup>178</sup></a> </p> <h2 id="clinical-significance">Clinical significance</h2> <h3>Aging</h3> <p class="note">See also: <a href="/facts/Neurobiological_effects_of_physical_exercise/kVVntCLn">Neurobiological effects of physical exercise § Structural growth</a>, <a href="/facts/Aging_brain/7hFvvqf0">Aging brain</a>, and <a href="/facts/Memory_and_aging/SMQTkjCM">Memory and aging</a></p> <p>Normal aging is associated with a gradual decline in some types of memory, including <a href="/facts/Episodic_memory/1QIEM9gQ">episodic memory</a> and <a href="/facts/Working_memory/kzeDD3KQ">working memory</a> (or <a href="/facts/Short-term_memory/xaFod2bp">short-term memory</a>). Because the hippocampus is thought to play a central role in memory, there has been considerable interest in the possibility that age-related declines could be caused by hippocampal deterioration.<a class="footnote-ref" id="fnref:179" href="#fn:179"><sup>179</sup></a> Some early studies reported substantial loss of neurons in the hippocampus of <a href="/facts/Old_age/nEpQmo9g">elderly people</a>, but later studies using more precise techniques found only minimal differences.<a class="footnote-ref" id="fnref:180" href="#fn:180"><sup>180</sup></a> Similarly, some <a href="/facts/MRI/Vh9yG9qq">MRI</a> studies have reported shrinkage of the hippocampus in elderly people, but other studies have failed to reproduce this finding. There is, however, a reliable relationship between the size of the hippocampus and memory performance; so that where there is age-related shrinkage, memory performance will be impaired.<a class="footnote-ref" id="fnref:181" href="#fn:181"><sup>181</sup></a> There are also reports that memory tasks tend to produce less hippocampal activation in the elderly than in the young.<a class="footnote-ref" id="fnref:182" href="#fn:182"><sup>182</sup></a> Furthermore, a <a href="/facts/Randomized_control_trial/LG9lkyVx">randomized control trial</a> published in 2011 found that <a href="/facts/Aerobic_exercise/T5E59k2L">aerobic exercise</a> could increase the size of the hippocampus in adults aged 55 to 80 and also improve spatial memory.<a class="footnote-ref" id="fnref:183" href="#fn:183"><sup>183</sup></a> </p> <h3>Dementia</h3> <p>In <a href="/facts/Alzheimer%27s_disease/w7Ad6tdg">Alzheimer's disease</a> (and other forms of <a href="/facts/Dementia/T0MRDE9I">dementia</a>), the hippocampus is one of the first regions of the brain to suffer damage;<a class="footnote-ref" id="fnref:184" href="#fn:184"><sup>184</sup></a> <a href="/facts/Short-term_memory/xaFod2bp">short-term memory loss</a> and <a href="/facts/Disorientation/LtTwMXqE">disorientation</a> are included among the early symptoms. Damage to the hippocampus can also result from oxygen starvation (<a href="/facts/Hypoxia_(medical)/JWV04G89">hypoxia</a>), <a href="/facts/Encephalitis/auHEjvrD">encephalitis</a>, or <a href="/facts/Medial_temporal_lobe_epilepsy/PgztEb3B">medial temporal lobe epilepsy</a>. People with extensive, bilateral hippocampal damage may experience <a href="/facts/Anterograde_amnesia/9peb9rmv">anterograde amnesia</a>: the inability to form and retain new <a href="/facts/Memory/zucwQIEX">memories</a>. Dementia, is very often caused by <a href="/facts/Cerebral_ischemia/QDYdeAxk">cerebral ischemia</a>, that is believed to trigger changes in the hippocampus. Changes in <a href="/facts/Hippocampal_subfields/7zqI8mXG">CA1</a>, the hippocampal area that underlies <a href="/facts/Episodic_memory/1QIEM9gQ">episodic memory</a>, cause episodic memory impairment, the earliest symptom of post-ischemic dementia.<a class="footnote-ref" id="fnref:185" href="#fn:185"><sup>185</sup></a> </p> <h3>Stress</h3> <p>The hippocampus contains high levels of <a href="/facts/Glucocorticoid_receptor/NUsGokjq">glucocorticoid receptors</a>, which make it more vulnerable to <a href="/facts/Chronic_stress/lA8Xql58">long-term stress</a> than most other <a href="/facts/List_of_regions_in_the_human_brain/N8r44v6P">brain areas</a>.<a class="footnote-ref" id="fnref:186" href="#fn:186"><sup>186</sup></a> There is evidence that humans having experienced severe, long-lasting traumatic stress show atrophy of the hippocampus more than of other parts of the brain.<a class="footnote-ref" id="fnref:187" href="#fn:187"><sup>187</sup></a> These effects show up in <a href="/facts/Post-traumatic_stress_disorder/9etKu7bX">post-traumatic stress disorder</a>,<a class="footnote-ref" id="fnref:188" href="#fn:188"><sup>188</sup></a> and they may contribute to the hippocampal atrophy reported in <a href="/facts/Schizophrenia/FMP4lQ57">schizophrenia</a><a class="footnote-ref" id="fnref:189" href="#fn:189"><sup>189</sup></a> and <a href="/facts/Major_depressive_disorder/l2lQeWqr">severe depression</a>.<a class="footnote-ref" id="fnref:190" href="#fn:190"><sup>190</sup></a> Anterior hippocampal volume in children is positively correlated with parental family income and this correlation is thought to be mediated by income related stress.<a class="footnote-ref" id="fnref:191" href="#fn:191"><sup>191</sup></a> A study has revealed atrophy as a result of depression, but this can be stopped with anti-depressants even if they are not effective in relieving other symptoms.<a class="footnote-ref" id="fnref:192" href="#fn:192"><sup>192</sup></a> </p><p>Chronic stress resulting in elevated levels of <a href="/facts/Glucocorticoid/2P91Aj3S">glucocorticoids</a>, notably of <a href="/facts/Cortisol/5IvRV0cm">cortisol</a>, is seen to be a cause of neuronal atrophy in the hippocampus. This atrophy results in a smaller hippocampal volume which is also seen in <a href="/facts/Cushing%27s_syndrome/AYW7Gjma">Cushing's syndrome</a>. The higher levels of cortisol in Cushing's syndrome is usually the result of medications taken for other conditions.<a class="footnote-ref" id="fnref:193" href="#fn:193"><sup>193</sup></a><a class="footnote-ref" id="fnref:194" href="#fn:194"><sup>194</sup></a> Neuronal loss also occurs as a result of impaired neurogenesis. Another factor that contributes to a smaller hippocampal volume is that of dendritic retraction where dendrites are shortened in length and reduced in number, in response to increased glucocorticoids. This dendritic retraction is reversible.<a class="footnote-ref" id="fnref:195" href="#fn:195"><sup>195</sup></a> After treatment with medication to reduce cortisol in Cushing's syndrome, the hippocampal volume is seen to be restored by as much as 10%.<a class="footnote-ref" id="fnref:196" href="#fn:196"><sup>196</sup></a> This change is seen to be due to the reforming of the dendrites.<a class="footnote-ref" id="fnref:197" href="#fn:197"><sup>197</sup></a> This dendritic restoration can also happen when stress is removed. There is, however, evidence derived mainly from studies using rats that stress occurring shortly after birth can affect hippocampal function in ways that persist throughout life.<a class="footnote-ref" id="fnref:198" href="#fn:198"><sup>198</sup></a> </p><p>Sex-specific responses to stress have also been demonstrated in the rat to have an effect on the hippocampus. Chronic stress in the male rat showed dendritic retraction and cell loss in the CA3 region but this was not shown in the female. This was thought to be due to neuroprotective ovarian hormones.<a class="footnote-ref" id="fnref:199" href="#fn:199"><sup>199</sup></a><a class="footnote-ref" id="fnref:200" href="#fn:200"><sup>200</sup></a> In rats, DNA damage increases in the hippocampus under conditions of stress.<a class="footnote-ref" id="fnref:201" href="#fn:201"><sup>201</sup></a> </p> <h3>Epilepsy</h3> <p>The hippocampus is one of the few brain regions where new neurons are generated. This process of <a href="/facts/Neurogenesis/XSteTv8s">neurogenesis</a> is confined to the dentate gyrus.<a class="footnote-ref" id="fnref:202" href="#fn:202"><sup>202</sup></a> Neurogenesis can be positively affected by exercise or negatively affected by <a href="/facts/Epileptic_seizure/zuIrQyze">epileptic seizures</a>.<a class="footnote-ref" id="fnref:203" href="#fn:203"><sup>203</sup></a> </p><p>Seizures in <a href="/facts/Temporal_lobe_epilepsy/PgztEb3B">temporal lobe epilepsy</a> can affect the normal development of new neurons and can cause tissue damage. <a href="/facts/Hippocampal_sclerosis/wqGzqqPB">Hippocampal sclerosis</a> specific to the mesial temporal lobe, is the most common type of such tissue damage.<a class="footnote-ref" id="fnref:204" href="#fn:204"><sup>204</sup></a><a class="footnote-ref" id="fnref:205" href="#fn:205"><sup>205</sup></a> It is not yet clear, however, whether the epilepsy is usually caused by hippocampal abnormalities or whether the hippocampus is damaged by cumulative effects of seizures.<a class="footnote-ref" id="fnref:206" href="#fn:206"><sup>206</sup></a> However, in experimental settings where repetitive seizures are artificially induced in animals, hippocampal damage is a frequent result. This may be a consequence of the concentration of excitable <a href="/facts/Glutamate_receptor/MGwpHHUA">glutamate receptors</a> in the hippocampus. Hyperexcitability can lead to <a href="/facts/Cytotoxicity/SQuTTLoL">cytotoxicity</a> and cell death.<a class="footnote-ref" id="fnref:207" href="#fn:207"><sup>207</sup></a> It may also have something to do with the hippocampus being a site where <a href="/facts/Neurogenesis/XSteTv8s">new neurons</a> continue to be created throughout life,<a class="footnote-ref" id="fnref:208" href="#fn:208"><sup>208</sup></a> and to abnormalities in this process.<a class="footnote-ref" id="fnref:209" href="#fn:209"><sup>209</sup></a> </p> <h3>Schizophrenia</h3> <p>The causes of <a href="/facts/Schizophrenia/FMP4lQ57">schizophrenia</a> are not well understood, but numerous abnormalities of brain structure have been reported. The most thoroughly investigated alterations involve the cerebral cortex, but effects on the hippocampus have also been described. Many reports have found reductions in the size of the hippocampus in people with schizophrenia.<a class="footnote-ref" id="fnref:210" href="#fn:210"><sup>210</sup></a><a class="footnote-ref" id="fnref:211" href="#fn:211"><sup>211</sup></a> The left hippocampus seems to be affected more than the right.<a class="footnote-ref" id="fnref:212" href="#fn:212"><sup>212</sup></a> The changes noted have largely been accepted to be the result of abnormal development. Some studies in humans suggest that hippocampal alterations play a role in causing psychotic symptoms that are the most important feature of schizophrenia.<a class="footnote-ref" id="fnref:213" href="#fn:213"><sup>213</sup></a><a class="footnote-ref" id="fnref:214" href="#fn:214"><sup>214</sup></a> It has been suggested that on the basis of experimental work using animals, hippocampal dysfunction might produce an alteration of dopamine release in the <a href="/facts/Basal_ganglia/d9mbF6p3">basal ganglia</a>, thereby indirectly affecting the integration of information in the <a href="/facts/Prefrontal_cortex/dypYIrwx">prefrontal cortex</a>.<a class="footnote-ref" id="fnref:215" href="#fn:215"><sup>215</sup></a> It has also been suggested that hippocampal dysfunction might account for the disturbances in long-term memory frequently observed.<a class="footnote-ref" id="fnref:216" href="#fn:216"><sup>216</sup></a> </p><p>MRI studies have found a smaller brain volume and larger <a href="/facts/Ventricular_system/VMuY39Kp">ventricles</a> in people with schizophrenia – however researchers do not know if the shrinkage is from the schizophrenia or from the medication.<a class="footnote-ref" id="fnref:217" href="#fn:217"><sup>217</sup></a><a class="footnote-ref" id="fnref:218" href="#fn:218"><sup>218</sup></a> The hippocampus and thalamus have been shown to be reduced in volume; and the volume of the <a href="/facts/Globus_pallidus/QSGvBlAh">globus pallidus</a> is increased. Cortical patterns are altered, and a reduction in the volume and thickness of the cortex particularly in the frontal and temporal lobes has been noted. It has further been proposed that many of the changes seen are present at the start of the disorder which gives weight to the theory that there is abnormal neurodevelopment.<a class="footnote-ref" id="fnref:219" href="#fn:219"><sup>219</sup></a> </p><p>The hippocampus has been seen as central to the pathology of schizophrenia, both in the neural and physiological effects.<a class="footnote-ref" id="fnref:220" href="#fn:220"><sup>220</sup></a> It has been generally accepted that there is an abnormal synaptic connectivity underlying schizophrenia. Several lines of evidence implicate changes in the synaptic organization and connectivity, in and from the hippocampus<a class="footnote-ref" id="fnref:221" href="#fn:221"><sup>221</sup></a> Many studies have found dysfunction in the synaptic circuitry within the hippocampus and its activity on the prefrontal cortex. The glutamatergic pathways have been seen to be largely affected. The subfield CA1 is seen to be the least involved of the other subfields,<a class="footnote-ref" id="fnref:222" href="#fn:222"><sup>222</sup></a><a class="footnote-ref" id="fnref:223" href="#fn:223"><sup>223</sup></a> and CA4 and the subiculum have been reported elsewhere as being the most implicated areas.<a class="footnote-ref" id="fnref:224" href="#fn:224"><sup>224</sup></a> The review concluded that the pathology could be due to genetics, faulty neurodevelopment or abnormal neural plasticity. It was further concluded that schizophrenia is not due to any known neurodegenerative disorder.<a class="footnote-ref" id="fnref:225" href="#fn:225"><sup>225</sup></a> <a href="/facts/DNA_oxidation/3KCAWz3x">Oxidative DNA damage</a> is substantially increased in the hippocampus of elderly patients with chronic <a href="/facts/Schizophrenia/FMP4lQ57">schizophrenia</a>.<a class="footnote-ref" id="fnref:226" href="#fn:226"><sup>226</sup></a> </p> <h3>Transient global amnesia</h3> <p><a href="/facts/Transient_global_amnesia/LYYr4lVF">Transient global amnesia</a> is a dramatic, sudden, temporary, near-total loss of short-term memory. Various causes have been hypothesized including ischemia, epilepsy, migraine<a class="footnote-ref" id="fnref:227" href="#fn:227"><sup>227</sup></a> and disturbance of cerebral venous blood flow,<a class="footnote-ref" id="fnref:228" href="#fn:228"><sup>228</sup></a> leading to <a href="/facts/Ischemia/ySL9xbCl">ischemia</a> of structures such as the hippocampus that are involved in memory.<a class="footnote-ref" id="fnref:229" href="#fn:229"><sup>229</sup></a> </p><p>There has been no scientific proof of any cause. However, <a href="/facts/Diffusion-weighted_MRI/XWM7g7zj">diffusion-weighted MRI</a> studies taken from 12 to 24 hours following an episode has shown there to be small dot-like lesions in the hippocampus. These findings have suggested a possible implication of CA1 neurons made vulnerable by metabolic stress.<a class="footnote-ref" id="fnref:230" href="#fn:230"><sup>230</sup></a> </p> <h3>PTSD</h3> <p>Some studies shows correlation of reduced hippocampus volume and <a href="/facts/Post-traumatic_stress_disorder/9etKu7bX">post-traumatic stress disorder</a> (PTSD).<a class="footnote-ref" id="fnref:231" href="#fn:231"><sup>231</sup></a><a class="footnote-ref" id="fnref:232" href="#fn:232"><sup>232</sup></a> A study of <a href="/facts/Vietnam_War/W0gfbGTE">Vietnam War</a> combat veterans with PTSD showed a 20% reduction in the volume of their hippocampus compared with veterans with no such symptoms.<a class="footnote-ref" id="fnref:233" href="#fn:233"><sup>233</sup></a> This finding was not replicated in those with chronic PTSD, traumatized at an <a href="/facts/Ramstein_air_show_disaster/SroIPt4y">air show plane crash in 1988</a> (Ramstein, Germany).<a class="footnote-ref" id="fnref:234" href="#fn:234"><sup>234</sup></a> It is also the case that non-combat twin brothers of <a href="/facts/Vietnam_veteran/aUkaGvkW">Vietnam veterans</a> with PTSD also had smaller hippocampi than other controls, raising questions about the nature of the correlation.<a class="footnote-ref" id="fnref:235" href="#fn:235"><sup>235</sup></a> A 2016 study strengthened the theory that a smaller hippocampus increases the risk for post-traumatic stress disorder, and a larger hippocampus increases the likelihood of efficacious treatment.<a class="footnote-ref" id="fnref:236" href="#fn:236"><sup>236</sup></a> </p> <h3>Microcephaly</h3> <p>Hippocampus atrophy has been characterized in those with <a href="/facts/Microcephaly/lv4QGEIa">microcephaly</a>.<a class="footnote-ref" id="fnref:237" href="#fn:237"><sup>237</sup></a> Mouse models with <a href="/facts/WDR62/fVqT4bBb">Wdr62</a> mutations which recapitulate human <a href="/facts/Point_mutation/q30PEGFd">point mutations</a> show a deficiency in hippocampal development, and <a href="/facts/Neurogenesis/XSteTv8s">neurogenesis</a>.<a class="footnote-ref" id="fnref:238" href="#fn:238"><sup>238</sup></a> </p> <h2 id="other-animals">Other animals</h2> <h3>Other vertebrates</h3> <p>Non-mammalian <a href="/facts/Vertebrate/tT54FSTT">vertebrates</a> lack a brain structure that looks like the mammalian hippocampus, but they have one that is considered <a href="/facts/Homology_(biology)/muctKlyT">homologous</a> to it. The hippocampus, is in essence part of the allocortex. Only mammals have a fully developed cortex, but the structure it evolved from, called the <a href="/facts/Pallium_(neuroanatomy)/gI4oWmUa">pallium</a>, is present in all vertebrates, even the most primitive ones such as the <a href="/facts/Lamprey/nxgTvh0z">lamprey</a> or <a href="/facts/Hagfish/pEgPuk4v">hagfish</a>.<a class="footnote-ref" id="fnref:239" href="#fn:239"><sup>239</sup></a><a class="footnote-ref" id="fnref:240" href="#fn:240"><sup>240</sup></a> The pallium is usually divided into three zones: medial, lateral and dorsal. The medial pallium forms the precursor of the hippocampus. It does not resemble the hippocampus visually because the layers are not warped into an S shape or enfolded by the dentate gyrus, but the homology is indicated by strong chemical and functional affinities. There is evidence that these hippocampal-like structures are involved in spatial cognition in <a href="/facts/Reptile/04n1uKf1">reptiles</a>, and in <a href="/facts/Fish/fln4gH9V">fish</a>.<a class="footnote-ref" id="fnref:241" href="#fn:241"><sup>241</sup></a> </p> <h4>Fish</h4> <p>In <a href="/facts/Teleost/1YULPGW5">teleost</a> fish, the forebrain is everted (like an inside-out sock) with structures that lie on the outside, as contrasted with other vertebrate structures that lie in the interior, next to the ventricles.<a class="footnote-ref" id="fnref:242" href="#fn:242"><sup>242</sup></a> One of the consequences of this is that the medial pallium, the hippocampal zone of a typical vertebrate, is thought to correspond to the lateral pallium of a typical fish.<a class="footnote-ref" id="fnref:243" href="#fn:243"><sup>243</sup></a> Several types of fish (particularly goldfish) have been shown experimentally to have strong spatial memory abilities, even forming <a href="/facts/Cognitive_map/XCPtee5S">cognitive maps</a> of the areas they inhabit.<a class="footnote-ref" id="fnref:244" href="#fn:244"><sup>244</sup></a> Studies in <a href="/facts/Goldfish/Wdkw4kIL">goldfish</a> show that damage to both the lateral pallium, and the medial pallium impairs spatial memory coding.<a class="footnote-ref" id="fnref:245" href="#fn:245"><sup>245</sup></a><a class="footnote-ref" id="fnref:246" href="#fn:246"><sup>246</sup></a> It is not clear if the medial pallium plays a similar role in basal vertebrates, such as <a href="/facts/Shark/rh5Cotvx">sharks</a> and <a href="/facts/Batomorphi/4w6wfqlh">rays</a>, or even <a href="/facts/Lamprey/nxgTvh0z">lampreys</a> and <a href="/facts/Hagfish/pEgPuk4v">hagfish</a>.<a class="footnote-ref" id="fnref:247" href="#fn:247"><sup>247</sup></a> The dorsolateral pallium of the teleost is considered as homologous to the hippocampus in terrestrial vertebrates.<a class="footnote-ref" id="fnref:248" href="#fn:248"><sup>248</sup></a> In 2023, the goldfish brain was mapped by molecular parcellization showing that its telencephalon subregions were homogeneous to the hippocampal subfields in the mouse.<a class="footnote-ref" id="fnref:249" href="#fn:249"><sup>249</sup></a> </p> <h4>Birds</h4> <p class="note">See also: <a href="/facts/Avian_pallium/WmNCjAlx">Avian pallium</a></p> <p>In birds, the correspondence is sufficiently well established that most anatomists refer to the medial pallial zone as the "avian hippocampus".<a class="footnote-ref" id="fnref:250" href="#fn:250"><sup>250</sup></a> Numerous species of birds have strong spatial skills, in particular those that cache (store) food. There is evidence that food-caching birds have a larger hippocampus than other types of birds and that damage to the hippocampus causes impairments in spatial memory.<a class="footnote-ref" id="fnref:251" href="#fn:251"><sup>251</sup></a> </p> <h3>Insects and molluscs</h3> <p>Some types of <a href="/facts/Insect/IgDNvnUL">insects</a> such as <a href="/facts/Cockroaches/mKJP7W6j">cockroaches</a>, and <a href="/facts/Molluscs/1elgknsQ">molluscs</a> such as the <a href="/facts/Octopus/z5uokKFF">octopus</a>, also have strong spatial learning and navigation abilities, but these appear to work differently from the mammalian spatial system, suggesting that there is no common evolutionary origin. <a href="/facts/Mushroom_bodies/os7jIITz">Mushroom bodies</a> in insect brains are associated with learning and memory carried out in the mammalian hippocampus.<a class="footnote-ref" id="fnref:252" href="#fn:252"><sup>252</sup></a> The brain of the octopus is arranged in a circle of lobes around the esophagus. The vertical lobe has been shown to be involved in forming long term memory, and is seen to be analogous to the mammalian hippocampus and <a href="/facts/Cerebellum/kBRS2Lou">cerebellum</a>, and also to share some functional features of the mushroom bodies in insects.<a class="footnote-ref" id="fnref:253" href="#fn:253"><sup>253</sup></a><a class="footnote-ref" id="fnref:254" href="#fn:254"><sup>254</sup></a> </p> <h2 id="see-also">See also</h2> <ul><li><a href="/facts/Visual_short-term_memory/Y2svNBX5">Visual short-term memory</a></li></ul> <h2 id="additional-images">Additional images</h2> <h2 id="further-reading">Further reading</h2> <p> This article was submitted to <i>WikiJournal of Medicine</i> for external <a href="/facts/Scholarly_peer_review/ufyrXAkW">academic peer review</a> in 2016 (<a href="https://en.wikiversity.org/wiki/talk:WikiJournal_of_Medicine/The_Hippocampus">reviewer reports</a>). The updated content was reintegrated into the Wikipedia page under a CC-BY-SA-3.0 license (<a href="https://en.wikipedia.org/w/index.php?title=Hippocampus&action=history&date-range-to=2017-02-27">2017</a>). The version of record as reviewed is: Marion Wright, et al. (11 March 2017). <a href="https://upload.wikimedia.org/wikiversity/en/4/4e/The_Hippocampus.pdf">"The Hippocampus"</a> (PDF). <i>WikiJournal of Medicine</i>. 4 (1). <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.15347%2FWJM%2F2017.003">10.15347/WJM/2017.003</a>. <a href="/facts/ISSN_(identifier)/DPAflDvU">ISSN</a> <a href="https://search.worldcat.org/issn/2002-4436">2002-4436</a>. <a href="/facts/WDQ_(identifier)/5Myy74K5">Wikidata</a> Q43997714. </p> <ul><li>Hasselmo ME, Hinman JR (October 2022). "Computational Neuroscience: Hippocampus.". In Pfaff DW, Volkow ND, Rubenstein JL (eds.). <i>Neuroscience in the 21st Century: From Basic to Clinical</i>. Cham: Springer International Publishing. pp. 3489–3503. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1007%2F978-3-030-88832-9_175">10.1007/978-3-030-88832-9_175</a>. <a href="/facts/ISBN_(identifier)/15AdSPa9">ISBN</a> 978-3-030-88832-9.</li> <li>Wechsler RT, Morss AM, Wustoff CJ, Caughey AB (2004). <a href="https://books.google.com/books?id=k8qv-6tqZL0C&pg=PA37"><i>Blueprints notes & cases: Neuroscience</i></a>. Oxford: Blackwell Publishing. p. 37. <a href="/facts/ISBN_(identifier)/15AdSPa9">ISBN</a> 978-1-4051-0349-7. <a href="https://web.archive.org/web/20160828034644/https://books.google.com/books?id=k8qv-6tqZL0C&pg=PA37">Archived</a> from the original on 2016-08-28. Retrieved 2016-03-05.</li> <li>Derdikman D, Knierim JJ, eds. (2014). <i>Space, Time and Memory in the Hippocampal Formation</i>. <a href="/facts/Springer_Science%2BBusiness_Media/nAesf6nT">Springer</a>. <a href="/facts/ISBN_(identifier)/15AdSPa9">ISBN</a> 978-3-7091-1292-2.</li></ul> <h2 id="external-links">External links</h2> Wikimedia Commons has media related to Hippocampus. <ul><li><a href="http://brainmaps.org/index.php?q=hippocampus">Stained brain slice images which include the "hippocampus"</a> at the <a href="/facts/BrainMaps/fpjYWc63">BrainMaps project</a></li> <li><a href="http://www.stanford.edu/group/maciverlab/hippocampal.html">Diagram of a Hippocampal Brain Slice</a></li> <li><a href="http://ccdb.ucsd.edu/sand/main?stype=lite&keyword=hippocampus&Submit=Go&event=display&start=1">Hippocampus – Cell Centered Database</a></li> <li><a href="http://www.temporal-lobe.com">Temporal-lobe.com An interactive diagram of the rat parahippocampal-hippocampal region</a></li> <li><a href="https://web.archive.org/web/20120309084137/http://www.brainnav.com/browse?highlight=8d89b5&specid=2">"Search Hippocampus on BrainNavigator"</a>. <i>via BrainNavigator</i>. Archived from <a href="http://www.brainnav.com/browse?highlight=8d89b5&specid=2">the original</a> on 2012-03-09.</li> <li><a href="https://hippocampome.org/php/index.php">Hippocampome.org</a> Wheeler DW, Kopsick JD, Sutton N, Tecuatl C, Komendantov AO, Nadella K, et al. (February 2024). <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10942544">"Hippocampome.org 2.0 is a knowledge base enabling data-driven spiking neural network simulations of rodent hippocampal circuits"</a>. <i>eLife</i>. 12. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.7554%2FeLife.90597">10.7554/eLife.90597</a>. <a href="/facts/PMC_(identifier)/dX1zMt71">PMC</a> <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10942544">10942544</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/38345923">38345923</a>.</li> <li><a href="https://web.archive.org/web/20110722072202/http://web.sc.itc.keio.ac.jp/anatomy/Rauber-Kopsch/web/abb2/png144/440.png">https://web.archive.org/web/20110722072202/http://web.sc.itc.keio.ac.jp/anatomy/Rauber-Kopsch/web/abb2/png144/440.png</a></li></ul> <h2 id="references">References</h2> <ol> <li id="fn:1"><p>Tatu L, Bogousslavsky J (December 2022). 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