Literature DB >> 26424880

Distinct Functional Modules for Discrete and Rhythmic Forelimb Movements in the Mouse Motor Cortex.

Riichiro Hira1, Shin-Ichiro Terada2, Masashi Kondo3, Masanori Matsuzaki4.   

Abstract

Movements of animals are composed of two fundamental dynamics: discrete and rhythmic movements. Although the movements with distinct dynamics are thought to be differently processed in the CNS, it is unclear how they are represented in the cerebral cortex. Here, we investigated the cortical representation of movement dynamics by developing prolonged transcranial optogenetic stimulation (pTOS) using awake, channelrhodopsin-2 transgenic mice. We found two domains that induced discrete forelimb movements in the forward and backward directions, and these sandwiched a domain that generated rhythmic forelimb movements. The forward discrete movement had an intrinsic velocity profile and the rhythmic movement had an intrinsic oscillation frequency. Each of the forward discrete and rhythmic domains possessed intracortical synaptic connections within its own domain, independently projected to the spinal cord, and weakened the neuronal activity and movement induction of the other domain. pTOS-induced movements were also classified as ethologically relevant movements. Forepaw-to-mouth movement was mapped in a part of the forward discrete domain, while locomotion-like movement was in a part of the rhythmic domain. Interestingly, photostimulation of the rhythmic domain resulted in a nonrhythmic, continuous lever-pull movement when a lever was present. The motor cortex possesses functional modules for distinct movement dynamics, and these can adapt to environmental constraints for purposeful movements. Significance statement: Animal behavior has discrete and rhythmic components, such as reaching and locomotion. It is unclear how these movements with distinct dynamics are represented in the cerebral cortex. We investigated the dynamics of movements induced by long-duration transcranial photostimulation on the dorsal cortex of awake channelrhodopsin-2 transgenic mice. We found two domains causing forward and backward discrete forelimb movements and a domain for rhythmic forelimb movements. A domain for forward discrete movement and a domain for rhythmic movement mutually weakened neuronal activity and movement size. The photostimulation of the rhythmic domain also induced nonrhythmic, lever-pull movement, when the lever was present. Thus, the motor cortex has functional modules with distinct dynamics, and each module retains flexibility for adaptation to different environments.
Copyright © 2015 the authors 0270-6474/15/3513311-12$15.00/0.

Entities:  

Keywords:  channelrhodopsin; complex movement; motor cortex; mouse; photostimulation

Mesh:

Substances:

Year:  2015        PMID: 26424880      PMCID: PMC6605479          DOI: 10.1523/JNEUROSCI.2731-15.2015

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  21 in total

1.  Intact skull chronic windows for mesoscopic wide-field imaging in awake mice.

Authors:  Gergely Silasi; Dongsheng Xiao; Matthieu P Vanni; Andrew C N Chen; Timothy H Murphy
Journal:  J Neurosci Methods       Date:  2016-04-19       Impact factor: 2.390

2.  Ipsilateral-Dominant Control of Limb Movements in Rodent Posterior Parietal Cortex.

Authors:  Shogo Soma; Junichi Yoshida; Shigeki Kato; Yukari Takahashi; Satoshi Nonomura; Yae K Sugimura; Alain Ríos; Masanori Kawabata; Kazuto Kobayashi; Fusao Kato; Yutaka Sakai; Yoshikazu Isomura
Journal:  J Neurosci       Date:  2018-11-26       Impact factor: 6.167

3.  Organization of the reach and grasp in head-fixed vs freely-moving mice provides support for multiple motor channel theory of neocortical organization.

Authors:  Ian Q Whishaw; Jamshid Faraji; Jessica Kuntz; Behroo Mirza Agha; Mukt Patel; Gerlinde A S Metz; Majid H Mohajerani
Journal:  Exp Brain Res       Date:  2017-03-18       Impact factor: 1.972

4.  Intracortical Microstimulation Maps of Motor, Somatosensory, and Posterior Parietal Cortex in Tree Shrews (Tupaia belangeri) Reveal Complex Movement Representations.

Authors:  Mary K L Baldwin; Dylan F Cooke; Leah Krubitzer
Journal:  Cereb Cortex       Date:  2017-02-01       Impact factor: 5.357

5.  Optogenetic fMRI and electrophysiological identification of region-specific connectivity between the cerebellar cortex and forebrain.

Authors:  Katrina Y Choe; Carlos F Sanchez; Neil G Harris; Thomas S Otis; Paul J Mathews
Journal:  Neuroimage       Date:  2018-02-27       Impact factor: 6.556

Review 6.  Learning in the Rodent Motor Cortex.

Authors:  Andrew J Peters; Haixin Liu; Takaki Komiyama
Journal:  Annu Rev Neurosci       Date:  2017-03-31       Impact factor: 12.449

7.  Moving slowly is hard for humans: limitations of dynamic primitives.

Authors:  Se-Woong Park; Hamal Marino; Steven K Charles; Dagmar Sternad; Neville Hogan
Journal:  J Neurophysiol       Date:  2017-03-29       Impact factor: 2.714

8.  Automated gesture tracking in head-fixed mice.

Authors:  A Giovannucci; E A Pnevmatikakis; B Deverett; T Pereira; J Fondriest; M J Brady; S S-H Wang; W Abbas; P Parés; D Masip
Journal:  J Neurosci Methods       Date:  2017-07-17       Impact factor: 2.390

9.  Orofacial Movements Involve Parallel Corticobulbar Projections from Motor Cortex to Trigeminal Premotor Nuclei.

Authors:  Nicole Mercer Lindsay; Per M Knutsen; Adrian F Lozada; Daniel Gibbs; Harvey J Karten; David Kleinfeld
Journal:  Neuron       Date:  2019-10-03       Impact factor: 17.173

10.  A Whole-brain Map of Long-range Inputs to GABAergic Interneurons in the Mouse Caudal Forelimb Area.

Authors:  Zhuonan Duan; Anan Li; Hui Gong; Xiangning Li
Journal:  Neurosci Bull       Date:  2020-01-19       Impact factor: 5.203

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.