Department of Physiology, Fujita Health University School of Medicine, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake 470-1192, Japan; Department of Neuroscience II, Research Institute of Environmental Medicine, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan; Department of Functional Anatomy & Neuroscience, Graduate School of Medicine, Nagoya University, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Department of Computational Biology, Fujita Health University School of Medicine, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake 470-1192, Japan; Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma 630-0192, Japan; International Center for Brain Science (ICBS), Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake 470-1192, Japan.
Curr Biol. 2023 Aug 21;33(16):3436-3451.e7. doi: 10.1016/j.cub.2023.07.013. Epub 2023 Aug 2.
During reward-based learning tasks, animals make orofacial movements that globally influence brain activity at the timings of reward expectation and acquisition. These orofacial movements are not explicitly instructed and typically appear along with goal-directed behaviors. Here, we show that reinforcing optogenetic stimulation of dopamine neurons in the ventral tegmental area (oDAS) in mice is sufficient to induce orofacial movements in the whiskers and nose without accompanying goal-directed behaviors. Pavlovian conditioning with a sensory cue and oDAS elicited cue-locked and oDAS-aligned orofacial movements, which were distinguishable by a machine-learning model. Inhibition or knockout of dopamine D1 receptors in the nucleus accumbens inhibited oDAS-induced motion but spared cue-locked motion, suggesting differential regulation of these two types of orofacial motions. In contrast, inactivation of the whisker primary motor cortex (wM1) abolished both types of orofacial movements. We found specific neuronal populations in wM1 representing either oDAS-aligned or cue-locked whisker movements. Notably, optogenetic stimulation of wM1 neurons successfully replicated these two types of movements. Our results thus suggest that accumbal D1-receptor-dependent and -independent neuronal signals converge in the wM1 for facilitating distinct uninstructed orofacial movements during a reward-based learning task.
在基于奖励的学习任务中,动物会做出口腔面部运动,这些运动在奖励预期和获取的时间点上全局性地影响大脑活动。这些口腔面部运动不是明确指示的,通常与目标导向行为一起出现。在这里,我们表明,强化腹侧被盖区(VTA)多巴胺神经元的光遗传学刺激(oDAS)足以诱导小鼠的胡须和鼻子的口腔面部运动,而无需伴随目标导向行为。用感觉线索和 oDAS 进行的条件反射诱发了线索锁定和 oDAS 对齐的口腔面部运动,这些运动可以通过机器学习模型区分。伏隔核中多巴胺 D1 受体的抑制或敲除抑制了 oDAS 诱导的运动,但保留了线索锁定的运动,表明这两种类型的口腔面部运动受到不同的调节。相比之下,胡须初级运动皮层(wM1)的失活消除了这两种类型的口腔面部运动。我们在 wM1 中发现了特定的神经元群体,它们分别代表 oDAS 对齐或线索锁定的胡须运动。值得注意的是,wM1 神经元的光遗传学刺激成功复制了这两种类型的运动。因此,我们的研究结果表明,伏隔核中 D1 受体依赖性和非依赖性神经元信号在 wM1 中汇聚,以促进基于奖励的学习任务中两种不同的非指令性口腔面部运动。