Hira Riichiro, Terada Shin-Ichiro, Kondo Masashi, Matsuzaki Masanori
Division of Brain Circuits, National Institute for Basic Biology, Myodaiji, Okazaki 444-8585, Japan, Department of Basic Biology, SOKENDAI, The Graduate University for Advanced Studies, Okazaki 444-8585, Japan.
Division of Brain Circuits, National Institute for Basic Biology, Myodaiji, Okazaki 444-8585, Japan, Laboratory of Cell Recognition and Pattern Formation, Graduate School of Biostudies, Kyoto University, Kyoto 606-8501, Japan, and.
J Neurosci. 2015 Sep 30;35(39):13311-22. doi: 10.1523/JNEUROSCI.2731-15.2015.
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.
离散运动和节律性运动。尽管人们认为具有不同动力学的运动在中枢神经系统中的处理方式不同,但它们在大脑皮层中是如何表征的尚不清楚。在这里,我们通过对清醒的、表达通道视紫红质-2的转基因小鼠进行长时间经颅光遗传学刺激(pTOS),研究了运动动力学的皮层表征。我们发现了两个诱导前肢向前和向后离散运动的区域,这两个区域夹着一个产生前肢节律性运动的区域。向前的离散运动具有内在的速度曲线,而节律性运动具有内在的振荡频率。向前离散区域和节律性区域各自在其自身区域内具有皮质内突触连接,独立投射到脊髓,并减弱另一个区域的神经元活动和运动诱导。pTOS诱导的运动也被分类为与行为学相关的运动。前爪到嘴的运动映射在向前离散区域的一部分,而类似 locomotion 的运动映射在节律性区域的一部分。有趣的是,当有杠杆存在时,对节律性区域的光刺激会导致非节律性的、连续的杠杆拉动运动。运动皮层具有用于不同运动动力学的功能模块,并且这些模块可以适应环境限制以进行有目的的运动。意义声明:动物行为具有离散和节律性成分,例如伸手和 locomotion。尚不清楚这些具有不同动力学的运动在大脑皮层中是如何表征的。我们研究了长时间经颅光刺激对清醒的、表达通道视紫红质-2的转基因小鼠背侧皮层诱导的运动动力学。我们发现了两个导致前肢向前和向后离散运动的区域以及一个前肢节律性运动的区域。向前离散运动区域和节律性运动区域相互减弱神经元活动和运动幅度。当有杠杆存在时,对节律性区域的光刺激也会诱导非节律性的杠杆拉动运动。因此,运动皮层具有具有不同动力学的功能模块,并且每个模块都保留了适应不同环境的灵活性。