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5-羟色胺对兔离体颈上交感神经节前纤维的去极化作用。

The depolarizing action of 5-hydroxytryptamine on rabbit isolated preganglionic cervical sympathetic nerves.

作者信息

Elliott P, Wallis D I

机构信息

Department of Physiology, University College, Cardiff, United Kingdom.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1988 Dec;338(6):608-15. doi: 10.1007/BF00165624.

Abstract

This study describes a depolarizing action of 5-hydroxytryptamine (5-HT) on rabbit isolated preganglionic cervical sympathetic nerves using an extracellular recording technique. From cumulative concentration-response curves for 5-HT (1 mumol/l-1 mmol/l), the mean maximal depolarization was shown to be 277 +/- 32 microV and EC50 was 9.4 mumol/l (6.5-13.6 mumol/l, geometric mean, 95% confidence limits, n = 42). The responses to 5-HT displayed marked tachyphylaxis. When cumulative concentration-response curves to 5-HT and 2-methyl-5-HT were determined in the same preparations (n = 4), the mean maximal response to 5-HT was 519 +/- 167 microV, EC50 32.2 mumol/l (8.8-118 mumol/l) and the mean maximal response to 2-methyl-5-HT was 317 +/- 63 microV, EC50 35.1 mumol/l (12.9-95.5 mumol/l, geometric means, 95% confidence limits). The action of selective 5-HT antagonists was tested on repeated cumulative concentration-response curves to 5-HT. Neither methiothepin (0.1-1 mumol/l, n = 3) nor ketanserin (0.1-1 mumol/l, n = 3) had an action on 5-HT responses. The selective 5-HT3 antagonists MDL 72222, ICS 205-930 and SDZ 206-830 were all potent antagonists of the 5-HT depolarizations. The action of these antagonists was quantified by determining the apparent pA2 from the dose ratios and a Schild plot.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究采用细胞外记录技术,描述了5-羟色胺(5-HT)对兔离体颈上交感神经节前神经的去极化作用。根据5-HT(1 μmol/L - 1 mmol/L)的累积浓度-反应曲线,平均最大去极化为277±32 μV,半数有效浓度(EC50)为9.4 μmol/L(几何均值6.5 - 13.6 μmol/L,95%置信区间,n = 42)。对5-HT的反应表现出明显的快速耐受。当在相同标本(n = 4)中测定5-HT和2-甲基-5-HT的累积浓度-反应曲线时,对5-HT的平均最大反应为519±167 μV,EC50为32.2 μmol/L(8.8 - 118 μmol/L),对2-甲基-5-HT的平均最大反应为317±63 μV,EC50为35.1 μmol/L(12.9 - 95.5 μmol/L,几何均值,95%置信区间)。在重复的5-HT累积浓度-反应曲线上测试了选择性5-HT拮抗剂的作用。甲硫噻吩(0.1 - 1 μmol/L,n = 3)和酮色林(0.1 - 1 μmol/L,n = 3)对5-HT反应均无作用。选择性5-HT3拮抗剂MDL 72222、ICS 205 - 930和SDZ 206 - 830均为5-HT去极化的强效拮抗剂。通过根据剂量比和Schild图确定表观pA2来量化这些拮抗剂的作用。(摘要截断于250字)

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