Loading…

Complementary Roles of Primate Dorsal Premotor and Pre-Supplementary Motor Areas to the Control of Motor Sequences

We are able to temporally organize multiple movements in a purposeful manner in everyday life. Both the dorsal premotor (PMd) area and pre-supplementary motor area (pre-SMA) are known to be involved in the performance of motor sequences. However, it is unclear how each area differentially contribute...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of neuroscience 2022-09, Vol.42 (36), p.6946-6965
Main Authors: Nakajima, Toshi, Hosaka, Ryosuke, Mushiake, Hajime
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c508t-3073d03c4617b21133ee764d7c3b238cdbd3c03ff40b82a7347ac22b11e245a53
cites
container_end_page 6965
container_issue 36
container_start_page 6946
container_title The Journal of neuroscience
container_volume 42
creator Nakajima, Toshi
Hosaka, Ryosuke
Mushiake, Hajime
description We are able to temporally organize multiple movements in a purposeful manner in everyday life. Both the dorsal premotor (PMd) area and pre-supplementary motor area (pre-SMA) are known to be involved in the performance of motor sequences. However, it is unclear how each area differentially contributes to controlling multiple motor sequences. To address this issue, we recorded single-unit activity in both areas while monkeys (one male, one female) performed sixteen motor sequences. Each sequence comprised either a series of two identical movements (repetition) or two different movements (nonrepetition). The sequence was initially instructed with visual signals but had to be remembered thereafter. Here, we showed that the activity of single neurons in both areas transitioned from reactive- to predictive encoding while motor sequences were memorized. In the memory-guided trials, in particular, the activity of PMd cells preferentially represented the second movement (2M) in the sequence leading to a reward generally regardless of the first movement (1M). Such activity frequently began even before the 1M in a prospective manner, and was enhanced in nonrepetition sequences. Behaviorally, a lack of the activity enhancement often resulted in premature execution of the 2M. In contrast, cells in pre-SMA instantiated particular sequences of actions by coordinating switching or nonswitching movements in sequence. Our findings suggest that PMd and pre-SMA play complementary roles within behavioral contexts: PMd preferentially controls the movement that leads to a reward rather than the sequence per se, whereas pre-SMA coordinates all elements in a sequence by integrating temporal orders of multiple movements. Although both dorsal premotor (PMd) area and pre-supplementary motor area (pre-SMA) are involved in the control of motor sequences, it is not clear how these two areas contribute to coordination of sequential movements differently. To address this issue, we directly compared neuronal activity in the two areas recorded while monkeys memorized and performed multiple motor sequences. Our findings suggest that PMd preferentially controls the final action that ultimately leads to a reward in a prospective manner, whereas the pre-SMA coordinates switching among multiple actions within the context of the sequence. Our findings are of significance to understand the distinct roles for motor-related areas in the planning and executing motor sequences and the pathophysiology
doi_str_mv 10.1523/JNEUROSCI.2356-21.2022
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9463987</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2702977171</sourcerecordid><originalsourceid>FETCH-LOGICAL-c508t-3073d03c4617b21133ee764d7c3b238cdbd3c03ff40b82a7347ac22b11e245a53</originalsourceid><addsrcrecordid>eNpdUU1P3DAUtKpWZaH9CyhSL1yy2O85cXKphNItUNFSseVsOc5LWZTEWzupxL_HYekKerKe5kMzHsaOBV-KDPD024_V7c31urpcAmZ5CmIJHOANW0S0TEFy8ZYtOCie5lLJA3YYwj3nXHGh3rMDzErFs5wvmK9cv-2op2E0_iG5cR2FxLXJT7_pzUjJF-eD6eJJvRudT8zQzEe6nrYvZN-fsDNPJiSjS8Y7Sio3jN51s9cOXdOfiQZL4QN715ou0Mfn94jdfl39qi7Sq-vzy-rsKrUZL8YUucKGo5W5UDUIgUikctkoizVgYZu6QcuxbSWvCzAKpTIWoBaCQGYmwyP2eee7neqeGhuzetPp7dzMP2hnNvo1Mmzu9G_3V5cyx7JQ0eDk2cC7mD2Mut8ES11nBnJT0PF3oVRKKBGpn_6j3rvJD7FeZAkoikIqjKx8x7LeheCp3YcRXM-z6v2sep5Vg9DzrFF4_LLKXvZvR3wEq4mgZQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2712888473</pqid></control><display><type>article</type><title>Complementary Roles of Primate Dorsal Premotor and Pre-Supplementary Motor Areas to the Control of Motor Sequences</title><source>PubMed Central</source><creator>Nakajima, Toshi ; Hosaka, Ryosuke ; Mushiake, Hajime</creator><creatorcontrib>Nakajima, Toshi ; Hosaka, Ryosuke ; Mushiake, Hajime</creatorcontrib><description>We are able to temporally organize multiple movements in a purposeful manner in everyday life. Both the dorsal premotor (PMd) area and pre-supplementary motor area (pre-SMA) are known to be involved in the performance of motor sequences. However, it is unclear how each area differentially contributes to controlling multiple motor sequences. To address this issue, we recorded single-unit activity in both areas while monkeys (one male, one female) performed sixteen motor sequences. Each sequence comprised either a series of two identical movements (repetition) or two different movements (nonrepetition). The sequence was initially instructed with visual signals but had to be remembered thereafter. Here, we showed that the activity of single neurons in both areas transitioned from reactive- to predictive encoding while motor sequences were memorized. In the memory-guided trials, in particular, the activity of PMd cells preferentially represented the second movement (2M) in the sequence leading to a reward generally regardless of the first movement (1M). Such activity frequently began even before the 1M in a prospective manner, and was enhanced in nonrepetition sequences. Behaviorally, a lack of the activity enhancement often resulted in premature execution of the 2M. In contrast, cells in pre-SMA instantiated particular sequences of actions by coordinating switching or nonswitching movements in sequence. Our findings suggest that PMd and pre-SMA play complementary roles within behavioral contexts: PMd preferentially controls the movement that leads to a reward rather than the sequence per se, whereas pre-SMA coordinates all elements in a sequence by integrating temporal orders of multiple movements. Although both dorsal premotor (PMd) area and pre-supplementary motor area (pre-SMA) are involved in the control of motor sequences, it is not clear how these two areas contribute to coordination of sequential movements differently. To address this issue, we directly compared neuronal activity in the two areas recorded while monkeys memorized and performed multiple motor sequences. Our findings suggest that PMd preferentially controls the final action that ultimately leads to a reward in a prospective manner, whereas the pre-SMA coordinates switching among multiple actions within the context of the sequence. Our findings are of significance to understand the distinct roles for motor-related areas in the planning and executing motor sequences and the pathophysiology of apraxia and/or Parkinson's diseases that disables skilled motor actions.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/JNEUROSCI.2356-21.2022</identifier><identifier>PMID: 35970560</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Motor task performance ; Presupplementary motor area ; Reinforcement ; Sequences ; Supplementary motor area ; Unit activity ; Visual signals</subject><ispartof>The Journal of neuroscience, 2022-09, Vol.42 (36), p.6946-6965</ispartof><rights>Copyright © 2022 the authors.</rights><rights>Copyright Society for Neuroscience Sep 7, 2022</rights><rights>Copyright © 2022 the authors 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-3073d03c4617b21133ee764d7c3b238cdbd3c03ff40b82a7347ac22b11e245a53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9463987/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9463987/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35970560$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakajima, Toshi</creatorcontrib><creatorcontrib>Hosaka, Ryosuke</creatorcontrib><creatorcontrib>Mushiake, Hajime</creatorcontrib><title>Complementary Roles of Primate Dorsal Premotor and Pre-Supplementary Motor Areas to the Control of Motor Sequences</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>We are able to temporally organize multiple movements in a purposeful manner in everyday life. Both the dorsal premotor (PMd) area and pre-supplementary motor area (pre-SMA) are known to be involved in the performance of motor sequences. However, it is unclear how each area differentially contributes to controlling multiple motor sequences. To address this issue, we recorded single-unit activity in both areas while monkeys (one male, one female) performed sixteen motor sequences. Each sequence comprised either a series of two identical movements (repetition) or two different movements (nonrepetition). The sequence was initially instructed with visual signals but had to be remembered thereafter. Here, we showed that the activity of single neurons in both areas transitioned from reactive- to predictive encoding while motor sequences were memorized. In the memory-guided trials, in particular, the activity of PMd cells preferentially represented the second movement (2M) in the sequence leading to a reward generally regardless of the first movement (1M). Such activity frequently began even before the 1M in a prospective manner, and was enhanced in nonrepetition sequences. Behaviorally, a lack of the activity enhancement often resulted in premature execution of the 2M. In contrast, cells in pre-SMA instantiated particular sequences of actions by coordinating switching or nonswitching movements in sequence. Our findings suggest that PMd and pre-SMA play complementary roles within behavioral contexts: PMd preferentially controls the movement that leads to a reward rather than the sequence per se, whereas pre-SMA coordinates all elements in a sequence by integrating temporal orders of multiple movements. Although both dorsal premotor (PMd) area and pre-supplementary motor area (pre-SMA) are involved in the control of motor sequences, it is not clear how these two areas contribute to coordination of sequential movements differently. To address this issue, we directly compared neuronal activity in the two areas recorded while monkeys memorized and performed multiple motor sequences. Our findings suggest that PMd preferentially controls the final action that ultimately leads to a reward in a prospective manner, whereas the pre-SMA coordinates switching among multiple actions within the context of the sequence. Our findings are of significance to understand the distinct roles for motor-related areas in the planning and executing motor sequences and the pathophysiology of apraxia and/or Parkinson's diseases that disables skilled motor actions.</description><subject>Motor task performance</subject><subject>Presupplementary motor area</subject><subject>Reinforcement</subject><subject>Sequences</subject><subject>Supplementary motor area</subject><subject>Unit activity</subject><subject>Visual signals</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpdUU1P3DAUtKpWZaH9CyhSL1yy2O85cXKphNItUNFSseVsOc5LWZTEWzupxL_HYekKerKe5kMzHsaOBV-KDPD024_V7c31urpcAmZ5CmIJHOANW0S0TEFy8ZYtOCie5lLJA3YYwj3nXHGh3rMDzErFs5wvmK9cv-2op2E0_iG5cR2FxLXJT7_pzUjJF-eD6eJJvRudT8zQzEe6nrYvZN-fsDNPJiSjS8Y7Sio3jN51s9cOXdOfiQZL4QN715ou0Mfn94jdfl39qi7Sq-vzy-rsKrUZL8YUucKGo5W5UDUIgUikctkoizVgYZu6QcuxbSWvCzAKpTIWoBaCQGYmwyP2eee7neqeGhuzetPp7dzMP2hnNvo1Mmzu9G_3V5cyx7JQ0eDk2cC7mD2Mut8ES11nBnJT0PF3oVRKKBGpn_6j3rvJD7FeZAkoikIqjKx8x7LeheCp3YcRXM-z6v2sep5Vg9DzrFF4_LLKXvZvR3wEq4mgZQ</recordid><startdate>20220907</startdate><enddate>20220907</enddate><creator>Nakajima, Toshi</creator><creator>Hosaka, Ryosuke</creator><creator>Mushiake, Hajime</creator><general>Society for Neuroscience</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20220907</creationdate><title>Complementary Roles of Primate Dorsal Premotor and Pre-Supplementary Motor Areas to the Control of Motor Sequences</title><author>Nakajima, Toshi ; Hosaka, Ryosuke ; Mushiake, Hajime</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-3073d03c4617b21133ee764d7c3b238cdbd3c03ff40b82a7347ac22b11e245a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Motor task performance</topic><topic>Presupplementary motor area</topic><topic>Reinforcement</topic><topic>Sequences</topic><topic>Supplementary motor area</topic><topic>Unit activity</topic><topic>Visual signals</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakajima, Toshi</creatorcontrib><creatorcontrib>Hosaka, Ryosuke</creatorcontrib><creatorcontrib>Mushiake, Hajime</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakajima, Toshi</au><au>Hosaka, Ryosuke</au><au>Mushiake, Hajime</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Complementary Roles of Primate Dorsal Premotor and Pre-Supplementary Motor Areas to the Control of Motor Sequences</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2022-09-07</date><risdate>2022</risdate><volume>42</volume><issue>36</issue><spage>6946</spage><epage>6965</epage><pages>6946-6965</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>We are able to temporally organize multiple movements in a purposeful manner in everyday life. Both the dorsal premotor (PMd) area and pre-supplementary motor area (pre-SMA) are known to be involved in the performance of motor sequences. However, it is unclear how each area differentially contributes to controlling multiple motor sequences. To address this issue, we recorded single-unit activity in both areas while monkeys (one male, one female) performed sixteen motor sequences. Each sequence comprised either a series of two identical movements (repetition) or two different movements (nonrepetition). The sequence was initially instructed with visual signals but had to be remembered thereafter. Here, we showed that the activity of single neurons in both areas transitioned from reactive- to predictive encoding while motor sequences were memorized. In the memory-guided trials, in particular, the activity of PMd cells preferentially represented the second movement (2M) in the sequence leading to a reward generally regardless of the first movement (1M). Such activity frequently began even before the 1M in a prospective manner, and was enhanced in nonrepetition sequences. Behaviorally, a lack of the activity enhancement often resulted in premature execution of the 2M. In contrast, cells in pre-SMA instantiated particular sequences of actions by coordinating switching or nonswitching movements in sequence. Our findings suggest that PMd and pre-SMA play complementary roles within behavioral contexts: PMd preferentially controls the movement that leads to a reward rather than the sequence per se, whereas pre-SMA coordinates all elements in a sequence by integrating temporal orders of multiple movements. Although both dorsal premotor (PMd) area and pre-supplementary motor area (pre-SMA) are involved in the control of motor sequences, it is not clear how these two areas contribute to coordination of sequential movements differently. To address this issue, we directly compared neuronal activity in the two areas recorded while monkeys memorized and performed multiple motor sequences. Our findings suggest that PMd preferentially controls the final action that ultimately leads to a reward in a prospective manner, whereas the pre-SMA coordinates switching among multiple actions within the context of the sequence. Our findings are of significance to understand the distinct roles for motor-related areas in the planning and executing motor sequences and the pathophysiology of apraxia and/or Parkinson's diseases that disables skilled motor actions.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>35970560</pmid><doi>10.1523/JNEUROSCI.2356-21.2022</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0270-6474
ispartof The Journal of neuroscience, 2022-09, Vol.42 (36), p.6946-6965
issn 0270-6474
1529-2401
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9463987
source PubMed Central
subjects Motor task performance
Presupplementary motor area
Reinforcement
Sequences
Supplementary motor area
Unit activity
Visual signals
title Complementary Roles of Primate Dorsal Premotor and Pre-Supplementary Motor Areas to the Control of Motor Sequences
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T11%3A33%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Complementary%20Roles%20of%20Primate%20Dorsal%20Premotor%20and%20Pre-Supplementary%20Motor%20Areas%20to%20the%20Control%20of%20Motor%20Sequences&rft.jtitle=The%20Journal%20of%20neuroscience&rft.au=Nakajima,%20Toshi&rft.date=2022-09-07&rft.volume=42&rft.issue=36&rft.spage=6946&rft.epage=6965&rft.pages=6946-6965&rft.issn=0270-6474&rft.eissn=1529-2401&rft_id=info:doi/10.1523/JNEUROSCI.2356-21.2022&rft_dat=%3Cproquest_pubme%3E2702977171%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c508t-3073d03c4617b21133ee764d7c3b238cdbd3c03ff40b82a7347ac22b11e245a53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2712888473&rft_id=info:pmid/35970560&rfr_iscdi=true