Blazquez Pablo M, Yakusheva Tatyana A
Department of Otolaryngology, Washington University School of Medicine, 4566 Scott Avenue, St. Louis, MO 63110, USA.
Department of Otolaryngology, Washington University School of Medicine, 4566 Scott Avenue, St. Louis, MO 63110, USA.
Cell Rep. 2015 May 19;11(7):1043-53. doi: 10.1016/j.celrep.2015.04.020. Epub 2015 May 7.
Data from in vitro and anesthetized preparations indicate that inhibition plays a major role in cerebellar cortex function. We investigated the role of GABA-A inhibition in the macaque cerebellar ventral-paraflocculus while animals performed oculomotor behaviors that are known to engage the circuit. We recorded Purkinje cell responses to these behaviors with and without application of gabazine, a GABA-A receptor antagonist, near the recorded neuron. Gabazine increased the neuronal responsiveness to saccades in all directions and the neuronal gain to VOR cancellation and pursuit, most significantly the eye and head velocity sensitivity. L-glutamate application indicated that these changes were not the consequence of increases in baseline firing rate. Importantly, gabazine did not affect behavior or efference copy, suggesting that only local computations were disrupted. Our data, collected while the cerebellum performs behaviorally relevant computations, indicate that inhibition is a potent regulatory mechanism for the control of input-output gain and spatial tuning in the cerebellar cortex.
来自体外和麻醉制剂的数据表明,抑制在小脑皮质功能中起主要作用。我们研究了GABA-A抑制在猕猴小脑腹侧副小叶中的作用,同时动物进行已知会激活该回路的动眼行为。我们记录了浦肯野细胞对这些行为的反应,记录神经元附近应用或未应用GABAA受体拮抗剂gabazine。Gabazine增加了神经元对所有方向扫视的反应性以及对前庭眼反射取消和追踪的神经元增益,最显著的是眼和头速度敏感性。应用L-谷氨酸表明这些变化不是基线放电率增加的结果。重要的是,gabazine不影响行为或传出副本,这表明只有局部计算受到干扰。我们在小脑进行与行为相关的计算时收集的数据表明,抑制是控制小脑皮质输入-输出增益和空间调谐的有效调节机制。