Premotor cortex

<h2 id="structure">Structure</h2>
The premotor cortex occupies the part of <a href="/facts/Brodmann_area_6/2alR8363">Brodmann area 6</a> that lies on the lateral surface of the cerebral hemisphere. The medial extension of area 6, onto the midline surface of the hemisphere, is the site of the <a href="/facts/Supplementary_motor_area/60NkA8Ka">supplementary motor area</a>, or SMA.
The premotor cortex can be distinguished from the primary motor cortex, Brodmann area 4, just posterior to it, based on two main anatomical markers. First, the primary motor cortex contains giant pyramidal cells called <a href="/facts/Betz_cells/xHjmWlev">Betz cells</a> in layer V, whereas giant pyramidal cells are less common and smaller in the premotor cortex. Second, the primary motor cortex is agranular: it lacks a layer IV marked by the presence of granule cells. The premotor cortex is dysgranular: it contains a faint layer IV.
The premotor cortex can be distinguished from Brodmann area 46 of the prefrontal cortex, just anterior to it, by the presence of a fully formed granular layer IV in area 46. The premotor cortex is therefore anatomically a transition between the agranular motor cortex and the granular, six-layered prefrontal cortex.
The premotor cortex has been divided into finer subregions on the basis of <a href="/facts/Cytoarchitecture/npnsdK3T">cytoarchitecture</a> (the appearance of the cortex under a microscope), cytohistochemistry (the manner in which the cortex appears when stained by various chemical substances), anatomical connectivity to other brain areas, and physiological properties.<a class="footnote-ref" id="fnref:1" href="#fn:1">1</a><a class="footnote-ref" id="fnref:2" href="#fn:2">2</a><a class="footnote-ref" id="fnref:3" href="#fn:3">3</a><a class="footnote-ref" id="fnref:4" href="#fn:4">4</a> These divisions are summarized below in Divisions of the premotor cortex.
The connectivity of the premotor cortex is diverse, partly because the premotor cortex itself is heterogenous and different subregions have different connectivity. Generally the premotor cortex has strong afferent (input) and efferent (output) connectivity to the <a href="/facts/Primary_motor_cortex/DqdaQMNg">primary motor cortex</a>, the <a href="/facts/Supplementary_motor_area/60NkA8Ka">supplementary motor area</a>, the superior and inferior <a href="/facts/Parietal_lobe/T74NKNTN">parietal cortex</a>, and <a href="/facts/Prefrontal_cortex/dypYIrwx">prefrontal cortex</a>. Subcortically it projects to the <a href="/facts/Spinal_cord/XbWLr917">spinal cord</a>, the <a href="/facts/Striatum/MjNnTjSd">striatum</a>, and the motor <a href="/facts/Thalamus/UHDtUStc">thalamus</a> among other structures.
In the study of neurolinguistics, the ventral premotor cortex has been implicated in motor vocabularies in both speech and manual gestures. A mental syllabary — a repository of gestural scores for the most highly used syllables in a language — has been linked to the ventral premotor cortex in a large-scale meta-analysis of functional imaging studies. A recent prospective fMRI study that was designed to distinguish phonemic and syllable representations in motor codes provided further evidence for this view by demonstrating adaptation effects in the ventral premotor cortex to repeating syllables.
The premotor cortex is now generally divided into four sections.<a class="footnote-ref" id="fnref:5" href="#fn:5">5</a><a class="footnote-ref" id="fnref:6" href="#fn:6">6</a><a class="footnote-ref" id="fnref:7" href="#fn:7">7</a> First it is divided into an upper (or dorsal) premotor cortex and a lower (or ventral) premotor cortex. Each of these is further divided into a region more toward the front of the brain (rostral premotor cortex) and a region more toward the back (caudal premotor cortex). A set of acronyms are commonly used: PMDr (premotor dorsal, rostral), PMDc (premotor dorsal, caudal), PMVr (premotor ventral, rostral), PMVc (premotor ventral, caudal). Some researchers, especially those who study the ventral premotor areas, use a different terminology. Field 7 or F7 denotes PMDr; F2 = PMDc; F5=PMVr; F4=PMVc.
These subdivisions of premotor cortex were originally described and remain primarily studied in the monkey brain. Exactly how they may correspond to areas of the human brain, or whether the organization in the human brain is somewhat different, is not yet clear.

<h3>PMDc (F2)</h3>
PMDc is often studied with respect to its role in guiding reaching.<a class="footnote-ref" id="fnref:8" href="#fn:8">8</a><a class="footnote-ref" id="fnref:9" href="#fn:9">9</a><a class="footnote-ref" id="fnref:10" href="#fn:10">10</a> Neurons in PMDc are active during reaching. When monkeys are trained to reach from a central location to a set of target locations, neurons in PMDc are active during the preparation for the reach and also during the reach itself. They are broadly tuned, responding best to one direction of reach and less well to different directions. Electrical stimulation of the PMDc on a behavioral time scale was reported to evoke a complex movement of the shoulder, arm, and hand that resembles reaching with the hand opened in preparation to grasp.<a class="footnote-ref" id="fnref:11" href="#fn:11">11</a>

<h3>PMDr(F7)</h3>
PMDr may participate in learning to associate arbitrary sensory stimuli with specific movements or learning arbitrary response rules.<a class="footnote-ref" id="fnref:12" href="#fn:12">12</a><a class="footnote-ref" id="fnref:13" href="#fn:13">13</a><a class="footnote-ref" id="fnref:14" href="#fn:14">14</a> In this sense, it may resemble the prefrontal cortex more than other motor cortex fields. It may also have some relation to eye movement. Electrical stimulation in the PMDr can evoke eye movements<a class="footnote-ref" id="fnref:15" href="#fn:15">15</a> and neuronal activity in the PMDr can be modulated by eye movement.<a class="footnote-ref" id="fnref:16" href="#fn:16">16</a>

<h3>PMVc(F4)</h3>
PMVc or F4 is often studied with respect to its role in the sensory guidance of movement. Neurons here are responsive to tactile stimuli, visual stimuli, and auditory stimuli.<a class="footnote-ref" id="fnref:17" href="#fn:17">17</a><a class="footnote-ref" id="fnref:18" href="#fn:18">18</a><a class="footnote-ref" id="fnref:19" href="#fn:19">19</a><a class="footnote-ref" id="fnref:20" href="#fn:20">20</a> These neurons are especially sensitive to objects in the space immediately surrounding the body, in so-called peripersonal space. Electrical stimulation of these neurons causes an apparent defensive movement as if protecting the body surface.<a class="footnote-ref" id="fnref:21" href="#fn:21">21</a><a class="footnote-ref" id="fnref:22" href="#fn:22">22</a> This premotor region may be part of a larger circuit for maintaining a margin of safety around the body and guiding movement with respect to nearby objects.<a class="footnote-ref" id="fnref:23" href="#fn:23">23</a>

<h3>PMVr(F5)</h3>
PMVr or F5 is often studied with respect to its role in shaping the hand during grasping and in interactions between the hand and the mouth.<a class="footnote-ref" id="fnref:24" href="#fn:24">24</a><a class="footnote-ref" id="fnref:25" href="#fn:25">25</a> Electrical stimulation of at least some parts of F5, when the stimulation is applied on a behavioral time scale, evokes a complex movement in which the hand moves to the mouth, closes in a grip, orients such that the grip faces the mouth, the neck turns to align the mouth to the hand, and the mouth opens.<a class="footnote-ref" id="fnref:26" href="#fn:26">26</a><a class="footnote-ref" id="fnref:27" href="#fn:27">27</a>
<a href="/facts/Mirror_neurons/xfbp6k0S">Mirror neurons</a> were first discovered in area F5 in the monkey brain by Rizzolatti and colleagues.<a class="footnote-ref" id="fnref:28" href="#fn:28">28</a><a class="footnote-ref" id="fnref:29" href="#fn:29">29</a> These neurons are active when the monkey grasps an object. Yet the same neurons become active when the monkey watches an experimenter grasp an object in the same way. The neurons are therefore both sensory and motor. Mirror neurons are proposed to be a basis for understanding the actions of others by internally imitating the actions using one's own motor control circuits.

<h2 id="history">History</h2>
In the earliest work on the motor cortex, researchers recognized only one cortical field involved in motor control. Campbell<a class="footnote-ref" id="fnref:30" href="#fn:30">30</a> in 1905 was the first to suggest that there might be two fields, a "primary" motor cortex and an "intermediate precentral" motor cortex. His reasons were largely based on cytoarchitectonics. The primary motor cortex contains cells with giant cell bodies known as "<a href="/facts/Betz_cells/xHjmWlev">Betz cells</a>". The <a href="/facts/Betz_cells/xHjmWlev">Betz cells</a> are rare or absent in the adjacent cortex.
On similar criteria Brodmann<a class="footnote-ref" id="fnref:31" href="#fn:31">31</a> in 1909 also distinguished between his area 4 (coextensive with the primary motor cortex) and his area 6 (coextensive with the premotor cortex).
Vogt and Vogt<a class="footnote-ref" id="fnref:32" href="#fn:32">32</a><a class="footnote-ref" id="fnref:33" href="#fn:33">33</a> in 1919 also suggested that motor cortex was divided into a primary motor cortex (area 4) and a higher-order motor cortex (area 6) adjacent to it. Furthermore, in their account, area 6 could be divided into 6a (the dorsal part) and 6b (the ventral part). The dorsal part could be further divided into 6a-alpha (a posterior part adjacent to the primary motor cortex) and 6a-beta (an anterior part adjacent to the prefrontal cortex). These cortical fields formed a hierarchy in which 6a-beta controlled movement at the most complex level, 6a-alpha had intermediate properties, and the primary motor cortex controlled movement at the simplest level. Vogt and Vogt are therefore the original source of the idea of a caudal (6a-alpha) and a rostral (6a-beta) premotor cortex.
Fulton<a class="footnote-ref" id="fnref:34" href="#fn:34">34</a> in 1935 helped to solidify the distinction between a primary motor map of the body in area 4 and a higher-order premotor cortex in area 6. His main evidence came from lesion studies in monkeys. It is not clear where the term "premotor" came from or who used it first, but Fulton popularized the term.
A caveat about the premotor cortex, noted early in its study, is that the hierarchy between the premotor cortex and the primary motor cortex is not absolute. Instead both the premotor cortex and primary motor cortex project directly to the spinal cord, and each has some capability to control movement even in the absence of the other. Therefore, the two cortical fields operate at least partly in parallel rather than in a strict hierarchy. This parallel relationship was noted as early as 1919 by Vogt and Vogt<a class="footnote-ref" id="fnref:35" href="#fn:35">35</a><a class="footnote-ref" id="fnref:36" href="#fn:36">36</a> and also emphasized by Fulton.<a class="footnote-ref" id="fnref:37" href="#fn:37">37</a>
<a href="/facts/Wilder_Penfield/hIpcRkUg">Penfield</a><a class="footnote-ref" id="fnref:38" href="#fn:38">38</a> in 1937 notably disagreed with the idea of a premotor cortex. He suggested that there was no functional distinction between a primary motor and a premotor area. In his view both were part of the same map. The most posterior part of the map, in area 4, emphasized the hand and fingers and the most anterior part, in area 6, emphasized the muscles of the back and neck.
Woolsey<a class="footnote-ref" id="fnref:39" href="#fn:39">39</a> who studied the motor map in monkeys in 1956 also believed there was no distinction between primary motor and premotor cortex. He used the term M1 for the proposed single map that encompassed both the primary motor cortex and the premotor cortex. He used the term M2 for the medial motor cortex now commonly known as the supplementary motor area. (Sometimes in modern reviews M1 is incorrectly equated with the primary motor cortex.)
Given this work by Penfield on the human brain and by Woolsey on the monkey brain, by the 1960s the idea of a lateral premotor cortex as separate from the primary motor cortex had mainly disappeared from the literature. Instead M1 was considered to be a single map of the body, perhaps with complex properties, arranged along the central sulcus.

<h3>Re-emergence</h3>
The hypothesis of a separate premotor cortex re-emerged and gained ground in the 1980s. Several key lines of research helped to establish the premotor cortex by showing that it had properties distinct from those of the adjacent primary motor cortex.
Roland and colleagues<a class="footnote-ref" id="fnref:40" href="#fn:40">40</a><a class="footnote-ref" id="fnref:41" href="#fn:41">41</a> studied the dorsal premotor cortex and the supplementary motor area in humans while blood flow in the brain was monitored in a positron emission scanner. When people made complex sensory-guided movements such as following verbal instructions, more blood flow was measured in the dorsal premotor cortex. When people made internally paced sequences of movements, more blood flow was measured in the supplementary motor area. When people made simple movements that required little planning, such as palpating an object with the hand, the blood flow was more limited to the primary motor cortex. By implication, the primary motor cortex was more involved in execution of simple movement, the premotor cortex was more involved in sensory guided movement, and the supplementary motor area was more involved in internally generated movements.
Wise and his colleagues<a class="footnote-ref" id="fnref:42" href="#fn:42">42</a><a class="footnote-ref" id="fnref:43" href="#fn:43">43</a> studied the dorsal premotor cortex of monkeys. The monkeys were trained to perform a delayed response task, making a movement in response to a sensory instruction cue. During the task, neurons in the dorsal premotor cortex became active in response to the sensory cue and often remained active during the few seconds of delay or preparation time before the monkey performed the instructed movement. Neurons in the primary motor cortex showed much less activity during the preparation period and were more likely to be active only during the movement itself. By implication, the dorsal premotor cortex was more involved in planning or preparing for movement and the primary motor cortex more involved in executing movement.
Rizzolatti and colleagues<a class="footnote-ref" id="fnref:44" href="#fn:44">44</a> divided the premotor cortex into four parts or fields based on cytoarchitectonics, two dorsal fields and two ventral fields. They then studied the properties of the ventral premotor fields, establishing tactile, visual, and motor properties of a complex nature (summarized in greater detail above in Divisions of the premotor cortex).<a class="footnote-ref" id="fnref:45" href="#fn:45">45</a><a class="footnote-ref" id="fnref:46" href="#fn:46">46</a><a class="footnote-ref" id="fnref:47" href="#fn:47">47</a>
At least three representations of the hand were reported in the motor cortex, one in the primary motor cortex, one in the ventral premotor cortex, and one in the dorsal premotor cortex.<a class="footnote-ref" id="fnref:48" href="#fn:48">48</a><a class="footnote-ref" id="fnref:49" href="#fn:49">49</a> By implication, at least three different cortical fields may exist, each one performing its own special function in relation to the fingers and wrist.
For these and other reasons, a consensus has now emerged that the lateral motor cortex does not consist of a single, simple map of the body, but instead contains multiple subregions including the primary motor cortex and several premotor fields. These premotor fields have diverse properties. Some project to the spinal cord and may play a direct role in movement control, whereas others do not. Whether these cortical areas are arranged in a hierarchy or share some other more complex relationship is still debated.
<a href="/facts/Michael_Graziano/ML2uQmHb">Graziano</a> and colleagues suggested an alternative principle of organization for the primary motor cortex and the caudal part of the premotor cortex, all regions that project directly to the spinal cord and that were included in the Penfield and Woolsey definition of M1. In this alternative proposal, the motor cortex is organized as a map of the natural behavioral repertoire.<a class="footnote-ref" id="fnref:50" href="#fn:50">50</a><a class="footnote-ref" id="fnref:51" href="#fn:51">51</a> The complicated, multifaceted nature of the behavioral repertoire results in a complicated, heterogeneous map in cortex, in which different parts of the movement repertoire are emphasized in different cortical subregions.
More complex movements such as reaching or climbing require more coordination among body parts, the processing of more complex control variables, the monitoring of objects in the space near the body, and planning several seconds into the future. Other parts of the movement repertoire, such as manipulating an object with the fingers once the object has been acquired, or manipulating an object in the mouth, involve less planning, less computation of spatial trajectory, and more control of individual joint rotations and muscle forces. In this view the more complex movements, especially multi-segmental movements, come to be emphasized in the more anterior part of the motor map because that cortex emphasizes the musculature of the back and neck which serves as the coordinating link between body parts. In contrast the simpler parts of the movement repertoire that tend to focus more on the distal musculature are emphasized in the more <a href="/facts/Posterior_cortex/f0d21cya">posterior cortex</a>. In this alternative view, though movements of lesser complexity are emphasized in the primary motor cortex and movements of greater complexity are emphasized in the caudal premotor cortex, this difference does not necessarily imply a control hierarchy. Instead the regions differ from each other, and contain subregions with differing properties, because the natural movement repertoire itself is heterogeneous.

<h2 id="references">References</h2>

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</ol>

Premotor cortex open-in-new

Premotor cortex