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毒蕈碱诱导大鼠前庭小脑浦肯野细胞自发放电性兴奋性突触后电流频率增加。

Muscarine-induced increase in frequency of spontaneous EPSCs in Purkinje cells in the vestibulo-cerebellum of the rat.

作者信息

Takayasu Yukihiro, Iino Masae, Furuya Nobuhiko, Ozawa Seiji

机构信息

Department of Physiology, Gunma University School of Medicine, Maebashi, Gunma, 371-8511, Japan.

出版信息

J Neurosci. 2003 Jul 16;23(15):6200-8. doi: 10.1523/JNEUROSCI.23-15-06200.2003.

Abstract

Cholinergic projections are relatively sparse in the cerebellum compared with other parts of the brain. However, some mossy fibers in the vestibulo-cerebellum are known to be cholinergic. To clarify the functional roles of cholinergic mossy fibers in the vestibulo-cerebellum, we investigated the effects of acetylcholine (ACh) on the membrane electrical properties of both granule cells and Purkinje cells in slices of the cerebellar vermis of the rat using whole-cell patch-clamp techniques. The bath application of ACh induced a marked increase in the frequency of spontaneous EPSCs (sEPSCs) in Purkinje cells specifically in the vestibulo-cerebellum. This effect of ACh was mimicked by muscarine but not by nicotine. It was abolished by application of either tetrodotoxin or the antagonist of AMPA receptors, indicating that the ACh-induced enhancement of sEPSCs occurred indirectly via the activation of neurons sending glutamatergic projections to Purkinje cells. In approximately 15% of granule cells tested in the vestibulo-cerebellum, muscarine elicited membrane depolarization accompanied by a decrease in membrane conductance and increased the neuronal excitability. The muscarine-induced depolarization of granule cells in the vestibulo-cerebellum was attributable to the inhibition of standing-outward K+ currents (IKSO) most likely via the activation of muscarinic M3 receptors. Taken together, these results indicate that ACh increases the firing frequency of granule cells by inhibiting IKSO, which in turn increases the frequency of sEPSCs in Purkinje cells in the rat vestibulo-cerebellum.

摘要

与大脑的其他部分相比,胆碱能投射在小脑中相对稀少。然而,已知前庭小脑的一些苔藓纤维是胆碱能的。为了阐明胆碱能苔藓纤维在前庭小脑中的功能作用,我们使用全细胞膜片钳技术研究了乙酰胆碱(ACh)对大鼠小脑蚓部切片中颗粒细胞和浦肯野细胞膜电特性的影响。浴用ACh可使浦肯野细胞中自发放电性兴奋性突触后电流(sEPSCs)的频率显著增加,特别是在前庭小脑中。ACh的这种作用可被毒蕈碱模拟,但不能被烟碱模拟。应用河豚毒素或AMPA受体拮抗剂可消除这种作用,这表明ACh诱导的sEPSCs增强是通过激活向浦肯野细胞发送谷氨酸能投射的神经元间接发生的。在前庭小脑中测试的约15%的颗粒细胞中,毒蕈碱引起膜去极化,同时膜电导降低,并增加了神经元兴奋性。前庭小脑中颗粒细胞的毒蕈碱诱导的去极化最有可能是通过毒蕈碱M3受体的激活抑制外向持续钾电流(IKSO)所致。综上所述,这些结果表明,ACh通过抑制IKSO增加颗粒细胞的放电频率,进而增加大鼠前庭小脑中浦肯野细胞的sEPSCs频率。

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