Li Hao, Feng Jingyu, Chen Mengying, Xin Min, Chen Xi, Liu Wenhao, Wang Liping, Wang Kuan Hong, He Jufang
Departments of Neuroscience and Biomedical Sciences, City University of Hong Kong, Hong Kong, China.
Centre for Regenerative Medicine and Health, Hong Kong Institute of Science & Innovation, Chinese Academy of Sciences, Hong Kong, China.
Elife. 2024 May 3;13:e83897. doi: 10.7554/eLife.83897.
Cholecystokinin (CCK) is an essential modulator for neuroplasticity in sensory and emotional domains. Here, we investigated the role of CCK in motor learning using a single pellet reaching task in mice. Mice with a knockout of gene () or blockade of CCK-B receptor (CCKBR) showed defective motor learning ability; the success rate of retrieving reward remained at the baseline level compared to the wildtype mice with significantly increased success rate. We observed no long-term potentiation upon high-frequency stimulation in the motor cortex of mice, indicating a possible association between motor learning deficiency and neuroplasticity in the motor cortex. In vivo calcium imaging demonstrated that the deficiency of CCK signaling disrupted the refinement of population neuronal activity in the motor cortex during motor skill training. Anatomical tracing revealed direct projections from CCK-expressing neurons in the rhinal cortex to the motor cortex. Inactivation of the CCK neurons in the rhinal cortex that project to the motor cortex bilaterally using chemogenetic methods significantly suppressed motor learning, and intraperitoneal application of CCK4, a tetrapeptide CCK agonist, rescued the motor learning deficits of mice. In summary, our results suggest that CCK, which could be provided from the rhinal cortex, may surpport motor skill learning by modulating neuroplasticity in the motor cortex.
胆囊收缩素(CCK)是感觉和情感领域神经可塑性的重要调节因子。在此,我们使用小鼠单颗粒抓取任务研究了CCK在运动学习中的作用。基因敲除()或CCK-B受体(CCKBR)阻断的小鼠表现出运动学习能力缺陷;与成功率显著提高的野生型小鼠相比,获取奖励的成功率维持在基线水平。我们在小鼠运动皮层高频刺激后未观察到长时程增强,这表明运动学习缺陷与运动皮层神经可塑性之间可能存在关联。体内钙成像显示,CCK信号的缺乏在运动技能训练期间破坏了运动皮层中群体神经元活动的精细化。解剖追踪显示,鼻周皮层中表达CCK的神经元直接投射到运动皮层。使用化学遗传学方法双侧失活投射到运动皮层的鼻周皮层中的CCK神经元可显著抑制运动学习,腹腔注射CCK4(一种四肽CCK激动剂)可挽救小鼠的运动学习缺陷。总之,我们的结果表明,可由鼻周皮层提供的CCK可能通过调节运动皮层的神经可塑性来支持运动技能学习。