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豚鼠膀胱条带中[3H]γ-氨基丁酸释放的调节

Regulation of [3H]GABA release from strips of guinea pig urinary bladder.

作者信息

Shirakawa J, Taniyama K, Iwai S, Tanaka C

机构信息

Department of Anesthesiology, Kobe University, School of Medicine, Japan.

出版信息

Am J Physiol. 1988 Dec;255(6 Pt 2):R888-93. doi: 10.1152/ajpregu.1988.255.6.R888.

Abstract

The presence of receptors that regulate the release of gamma-aminobutyric acid (GABA) was studied in strips of the guinea pig urinary bladder. GABA (10(-8)-10(-5) M) and muscimol (10(-8)-10(-5) M), but not baclofen (10(-5) M), reduced the Ca2+-dependent, tetrodotoxin-resistant release of [3H]GABA evoked by high K+ from the urinary bladder strips preloaded with [3H]GABA. The inhibitory effect of muscimol was antagonized by bicuculline and potentiated by diazepam, clonazepam, and pentobarbital sodium. The potentiating effect of clonazepam was antagonized by Ro 15-1788. Acetylcholine (ACh) inhibited the high K+-evoked release of [3H]GABA. The inhibitory effect of ACh was antagonized by atropine sulfate and pirenzepine but not by hexamethonium. Norepinephrine (NE) inhibited the evoked release of [3H]GABA. The inhibitory effect of NE was mimicked by clonidine, but not by phenylephrine, and was antagonized by yohimbine but not by prazosin. These results provide evidence that the release of GABA from strips of guinea pig urinary bladder is regulated via the bicuculline-sensitive GABAA receptor, M1-muscarinic, and alpha 2-adrenergic receptors.

摘要

在豚鼠膀胱条带中研究了调节γ-氨基丁酸(GABA)释放的受体的存在情况。GABA(10^(-8)-10^(-5)M)和蝇蕈醇(10^(-8)-10^(-5)M),但巴氯芬(10^(-5)M)不行,可减少预先用[3H]GABA加载的膀胱条带中高钾诱发的[3H]GABA的钙依赖性、河豚毒素抗性释放。蝇蕈醇的抑制作用被荷包牡丹碱拮抗,被地西泮、氯硝西泮和戊巴比妥钠增强。氯硝西泮的增强作用被Ro 15-1788拮抗。乙酰胆碱(ACh)抑制高钾诱发的[3H]GABA释放。ACh的抑制作用被硫酸阿托品和哌仑西平拮抗,但不被六甲铵拮抗。去甲肾上腺素(NE)抑制诱发的[3H]GABA释放。NE的抑制作用被可乐定模拟,但不被去氧肾上腺素模拟,且被育亨宾拮抗但不被哌唑嗪拮抗。这些结果提供了证据,表明豚鼠膀胱条带中GABA的释放是通过荷包牡丹碱敏感的GABAA受体、M1-毒蕈碱受体和α2-肾上腺素能受体调节的。

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