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促肾上腺皮质激素释放因子通过调节钠、钾和Ih电流增加浦肯野神经元的兴奋性。

Corticotropin-releasing factor increases Purkinje neuron excitability by modulating sodium, potassium, and Ih currents.

作者信息

Libster Avraham M, Title Ben, Yarom Yosef

机构信息

Edmond & Lily Safra Center for Brain Sciences, Department of Neurobiology, Institute of Life Sciences, The Hebrew University, Jerusalem, Israel

Edmond & Lily Safra Center for Brain Sciences, Department of Neurobiology, Institute of Life Sciences, The Hebrew University, Jerusalem, Israel.

出版信息

J Neurophysiol. 2015 Dec;114(6):3339-50. doi: 10.1152/jn.00745.2015. Epub 2015 Oct 7.

Abstract

Corticotropin-releasing factor (CRF) is a neuromodulator closely associated with stress responses. It is synthesized and released in the central nervous system by various neurons, including neurons of the inferior olive. The targets of inferior olivary neurons, the cerebellar Purkinje neurons (PNs), are endowed with CRF receptors. CRF increases the excitability of PNs in vivo, but the biophysical mechanism is not clear. Here we examine the effect of CRF on the firing properties of PNs using acute rat cerebellar slices. CRF increased the PN firing rate, regardless of whether they were firing tonically or switching between firing and quiescent periods. Current- and voltage-clamp experiments showed that the increase in firing rate was associated with a voltage shift of the activation curve of the persistent sodium current and hyperpolarizing-activated current, as well as activation of voltage-dependent potassium current. The multiple effects on various ionic currents, which are in agreement with the possibility that activation of CRF receptors triggers several intracellular pathways, are manifested as an increase excitability of PN.

摘要

促肾上腺皮质激素释放因子(CRF)是一种与应激反应密切相关的神经调质。它由包括下橄榄核神经元在内的各种神经元在中枢神经系统中合成并释放。下橄榄核神经元的靶标,即小脑浦肯野神经元(PNs),具有CRF受体。CRF在体内可增加PNs的兴奋性,但其生物物理机制尚不清楚。在这里,我们使用急性大鼠小脑切片研究了CRF对PNs放电特性的影响。无论PNs是持续放电还是在放电和静息期之间切换,CRF均增加了其放电频率。电流钳和电压钳实验表明,放电频率的增加与持续性钠电流和超极化激活电流激活曲线的电压偏移以及电压依赖性钾电流的激活有关。对各种离子电流的多种影响与CRF受体激活触发多种细胞内途径的可能性一致,表现为PNs兴奋性增加。

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