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速尿在成年大鼠高尔基细胞与颗粒细胞突触处显示出异质性GABA(A)受体表达。

Furosemide reveals heterogeneous GABA(A) receptor expression at adult rat Golgi cell to granule cell synapses.

作者信息

Wall Mark J

机构信息

Neurobiology Group, Department of Biological Sciences, University of Warwick, Coventry CV4 7AL, UK.

出版信息

Neuropharmacology. 2002 Sep;43(4):737-49. doi: 10.1016/s0028-3908(02)00085-0.

Abstract

The contribution that alpha6 subunit-containing GABA(A) receptors make to inhibitory synaptic transmission to granule cells was investigated by making whole-cell patch clamp recordings from granule cells in adult rat cerebellar slices and applying furosemide, the specific alpha6 subunit-containing GABA(A) receptor antagonist. Endogenous, extracellular GABA continually activated GABA(A) receptors producing a tonic current. Since this current was markedly reduced by furosemide it was probably produced by alpha6 subunit-containing receptors. In contrast, furosemide had little effect on the amplitude or kinetics of fast spontaneous inhibitory postsynaptic currents (sIPSCs), although such sIPSCs were abolished by bicuculline and SR95331. However, the amplitude of evoked IPSCs with a very slow rise and decay were markedly reduced by furosemide. These IPSCs probably resulted from the spillover of GABA from neighbouring synapses activating high affinity alpha6 subunit-containing receptors. In the rest of the cells (40 out of 46), evoked IPSCs had rise and decay kinetics that lay in-between fast sIPSCs and slow 'spillover' IPSCs. Such IPSCs had variable kinetics and also exhibited considerable variation in the magnitude of furosemide block. Thus the GABA(A) receptors present at adult Golgi cell-granule cell synapses, at a developmental stage where receptor expression is complete, are highly heterogeneous.

摘要

通过对成年大鼠小脑切片中的颗粒细胞进行全细胞膜片钳记录,并应用速尿(一种特异性的含α6亚基的GABA(A)受体拮抗剂),研究了含α6亚基的GABA(A)受体对颗粒细胞抑制性突触传递的贡献。内源性细胞外GABA持续激活GABA(A)受体,产生一种强直电流。由于这种电流被速尿显著降低,它可能是由含α6亚基的受体产生的。相比之下,速尿对快速自发抑制性突触后电流(sIPSCs)的幅度或动力学影响很小,尽管这种sIPSCs被荷包牡丹碱和SR95331消除。然而,上升和衰减非常缓慢的诱发IPSCs的幅度被速尿显著降低。这些IPSCs可能是由于来自相邻突触的GABA溢出激活了含高亲和力α6亚基的受体所致。在其余的细胞中(46个中的40个),诱发IPSCs的上升和衰减动力学介于快速sIPSCs和缓慢的“溢出”IPSCs之间。这种IPSCs具有可变的动力学,并且在速尿阻断的幅度上也表现出相当大的变化。因此,在受体表达完成的发育阶段,成年高尔基细胞 - 颗粒细胞突触处存在的GABA(A)受体具有高度异质性。

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