Center of Basic Research, Biomedical Research Foundation Academy of Athens, Athens 11527, Greece.
School of Psychology and Neuroscience, University of St. Andrews, St. Andrews KY16 9JP, United Kingdom.
Proc Natl Acad Sci U S A. 2023 Sep 26;120(39):e2300348120. doi: 10.1073/pnas.2300348120. Epub 2023 Sep 21.
The intensity of muscle contraction, and therefore movement vigor, needs to be adaptable to enable complex motor behaviors. This can be achieved by adjusting the properties of motor neurons, which form the final common pathway for all motor output from the central nervous system. Here, we identify roles for a neuropeptide, cocaine- and amphetamine-regulated transcript (CART), in the control of movement vigor. We reveal distinct but parallel mechanisms by which CART and acetylcholine, both released at C bouton synapses on motor neurons, selectively amplify the output of subtypes of motor neurons that are recruited during intense movement. We find that mice with broad genetic deletion of CART or selective elimination of acetylcholine from C boutons exhibit deficits in behavioral tasks that require higher levels of motor output. Overall, these data uncover spinal modulatory mechanisms that control movement vigor to support movements that require a high degree of muscle force.
肌肉收缩的强度,进而运动活力,需要具有适应性,以实现复杂的运动行为。这可以通过调节运动神经元的特性来实现,运动神经元是中枢神经系统所有运动输出的最终共同途径。在这里,我们确定了一种神经肽——可卡因和安非他命调节转录物(CART)在控制运动活力中的作用。我们揭示了 CART 和乙酰胆碱以不同但平行的机制,选择性放大运动神经元亚型的输出,这些亚型在剧烈运动时被募集。我们发现,CART 广泛遗传缺失或 C 末梢乙酰胆碱选择性消除的小鼠在需要更高运动输出水平的行为任务中表现出缺陷。总的来说,这些数据揭示了控制运动活力的脊髓调节机制,以支持需要高度肌肉力量的运动。