Optophysiology Lab, Institute of Biology III, University of Freiburg, Freiburg 79104, Germany
Optophysiology Lab, Institute of Biology III, University of Freiburg, Freiburg 79104, Germany.
eNeuro. 2021 Mar 9;8(2). doi: 10.1523/ENEURO.0453-20.2021. Print 2021 Mar-Apr.
Tactile sensation is one of our primary means to collect information about the nearby environment and thus crucial for daily activities and survival. Therefore, it is of high importance to restore sensory feedback after sensory loss. Optogenetic manipulation allows local or pathway-specific write-in of information. However, it remains elusive whether optogenetic stimulation can be interpreted as tactile sensation to guide operant behavior and how it is integrated with tactile stimuli. To address these questions, we employed a vibrotactile detection task combined with optogenetic neuromodulation in freely moving rats. By bidirectionally manipulating the activity of neurons in primary somatosensory cortex (S1), we demonstrated that optical activation as well as inhibition of S1 reduced the detection rate for vibrotactile stimuli. Interestingly, activation of corticostriatal terminals improved the detection of tactile stimuli, while inhibition of corticostriatal terminals did not affect the performance. To manipulate the corticostriatal pathway more specifically, we employed a dual viral system. Activation of corticostriatal cell bodies disturbed the tactile perception while activation of corticostriatal terminals slightly facilitated the detection of vibrotactile stimuli. In the absence of tactile stimuli, both corticostriatal cell bodies as well as terminals caused a reaction. Taken together, our data confirmed the possibility to restore sensation using optogenetics and demonstrated that S1 and its descending projections to striatum play differential roles in the neural processing underlying vibrotactile detection.
触觉是我们收集周围环境信息的主要方式之一,因此对日常活动和生存至关重要。因此,恢复感觉丧失后的感觉反馈非常重要。光遗传学操作允许局部或特定路径的信息写入。然而,光遗传学刺激是否可以被解释为触觉感觉以指导操作性行为,以及它如何与触觉刺激整合,仍然难以捉摸。为了解决这些问题,我们在自由移动的大鼠中采用了振动触觉检测任务结合光遗传学神经调节。通过双向操纵初级体感皮层(S1)中的神经元活动,我们证明了 S1 的光激活和抑制都降低了对振动触觉刺激的检测率。有趣的是,皮质纹状体末端的激活改善了触觉刺激的检测,而皮质纹状体末端的抑制并不影响性能。为了更具体地操纵皮质纹状体通路,我们采用了双重病毒系统。皮质纹状体细胞体的激活扰乱了触觉感知,而皮质纹状体末端的激活略微促进了对振动触觉刺激的检测。在没有触觉刺激的情况下,皮质纹状体细胞体和末端都会引起反应。总之,我们的数据证实了使用光遗传学恢复感觉的可能性,并表明 S1 及其向纹状体的下行投射在振动触觉检测的神经处理中发挥了不同的作用。