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牛肾上腺髓质嗜铬细胞上GABAA受体特性与功能的电生理研究

An electrophysiological investigation of the characteristics and function of GABAA receptors on bovine adrenomedullary chromaffin cells.

作者信息

Peters J A, Lambert J J, Cottrell G A

机构信息

Department of Pharmacology and Clinical Pharmacology, Ninewells Hospital, Medical School, University of Dundee, Great Britain.

出版信息

Pflugers Arch. 1989 Oct;415(1):95-103. doi: 10.1007/BF00373146.

Abstract

The characteristics and function of gamma-aminobutyric acidA (GABAA) receptors expressed on bovine chromaffin cells in culture have been investigated using patch-clamp techniques. In voltage-clamped whole-cells, locally applied GABA (100 microM) evoked a transmembrane chloride current which demonstrated outward rectification. The amplitude of such currents was reversibly suppressed by the GABAA receptor antagonists bicuculline, picrotoxin and RU5135, and enhanced by the general anaesthetic propanidid. Glycine (100 microM) and baclofen (100 microM) were ineffective as agonists. In support of a physiological role for GABA in the adrenal medulla, the co-existence of GABAA and nicotinic acetylcholine (ACh) receptors was demonstrated on whole cells and outside-out membrane patches. Ionophoretically applied GABA reduced the amplitude of depolarization and action potential discharge occurring in response to locally applied ACh (100 microM), but had no effect upon the underlying ACh-induced current. In addition, an excitatory action of GABA was demonstrated by recording action potential waveforms in cell-attached patches. The results are discussed in the context of a GABA-ergic regulation of catecholamine secretion.

摘要

利用膜片钳技术研究了培养的牛嗜铬细胞上表达的γ-氨基丁酸A(GABAA)受体的特性和功能。在电压钳制的全细胞中,局部施加的GABA(100微摩尔)诱发了一种跨膜氯离子电流,该电流表现出外向整流。此类电流的幅度被GABAA受体拮抗剂荷包牡丹碱、印防己毒素和RU5135可逆性抑制,并被全身麻醉剂丙泮尼地增强。甘氨酸(100微摩尔)和巴氯芬(100微摩尔)作为激动剂无效。为支持GABA在肾上腺髓质中的生理作用,在全细胞和外侧向外膜片上证实了GABAA和烟碱型乙酰胆碱(ACh)受体共存。离子电泳施加的GABA降低了对局部施加的ACh(100微摩尔)产生的去极化幅度和动作电位发放,但对潜在的ACh诱导电流没有影响。此外,通过记录细胞贴附片上的动作电位波形证实了GABA的兴奋作用。在儿茶酚胺分泌的GABA能调节背景下讨论了这些结果。

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