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去甲肾上腺素通过β-肾上腺素能受体促进绒球中小脑平行纤维到浦肯野细胞突触处的长时程抑制的诱导。

Norepinephrine Facilitates Induction of Long-term Depression through β-Adrenergic Receptor at Parallel Fiber-to-Purkinje Cell Synapses in the Flocculus.

作者信息

Inoshita Takuma, Hirano Tomoo

机构信息

Department of Biophysics, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan.

Department of Biophysics, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan.

出版信息

Neuroscience. 2021 May 10;462:141-150. doi: 10.1016/j.neuroscience.2020.05.037. Epub 2020 Jun 2.

Abstract

The cerebellum is involved in motor learning, and long-term depression (LTD) at parallel fiber-to-Purkinje cell (PF-PC) synapses has been considered to be a primary cellular mechanism for motor learning. In addition, the contribution of norepinephrine (NE) to cerebellum-dependent learning paradigms has been reported. Thus, the roles of LTD and of NE in motor learning have been studied separately, and the relationship between the effects of NE and LTD remains unclear. Here, we examined effects of β-adrenergic receptor (β-AR) activity on the synaptic transmission and LTD at PF-PC synapses in the cerebellar flocculus. The flocculus regulates adaptation of oculomotor reflexes, and we previously reported the involvement of both LTD and β-AR in adaptation of an oculomotor reflex. Here we found that specific agonists for β-AR or NE did not directly change synaptic transmission, but lowered the threshold for LTD induction at PF-PC synapses in the flocculus. In addition, protein kinase A (PKA), which is activated downstream of β-AR, facilitated the LTD induction. Altogether, these results suggest that NE facilitates LTD induction at PF-PC synapses in the flocculus by activating PKA through β-AR.

摘要

小脑参与运动学习,平行纤维到浦肯野细胞(PF-PC)突触处的长时程抑制(LTD)被认为是运动学习的主要细胞机制。此外,已有报道称去甲肾上腺素(NE)对小脑依赖的学习范式有作用。因此,LTD和NE在运动学习中的作用是分别进行研究的,而NE与LTD效应之间的关系仍不清楚。在此,我们研究了β-肾上腺素能受体(β-AR)活性对小脑绒球PF-PC突触处突触传递和LTD的影响。绒球调节动眼反射的适应性,我们之前报道过LTD和β-AR都参与了动眼反射的适应性。在此我们发现,β-AR或NE的特异性激动剂不会直接改变突触传递,但会降低绒球中PF-PC突触处LTD诱导的阈值。此外,在β-AR下游被激活的蛋白激酶A(PKA)促进了LTD的诱导。总之,这些结果表明,NE通过β-AR激活PKA,促进了绒球中PF-PC突触处的LTD诱导。

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