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大鼠皮肤电反应的生理与药理学分析

A physiological and pharmacological analysis of the electrodermal response in the rat.

作者信息

Girardot M N, Koss M C

出版信息

Eur J Pharmacol. 1984 Feb 17;98(2):185-91. doi: 10.1016/0014-2999(84)90589-2.

Abstract

Electrodermal responses (EDR) of the sympathetic-cholinergic sudomotor system were elicited in the footpads of the hindpaws of anesthetized rats. The most reactive CNS loci were caudal to the region of the posterior hypothalamus. Peripherally evoked responses were elicited by electrical stimulation of the decentralized tibial nerve. The amplitude of these evoked EDR was stable over time and both the centrally and peripherally elicited responses were frequency-dependent. Atropine (200 micrograms/kg) depressed the EDR elicited by both peripheral and central stimulation whereas hexamethonium (20 mg/kg) only inhibited the central EDR. Clonidine had no effect on the EDR evoked at the periphery but produced a significant dose-dependent depressant effect on the centrally evoked EDR; this effect was partially antagonized by yohimbine (0.75 mg/kg). It is suggested that the rat is a suitable species for the use of the sudomotor system in the investigation of adrenergic agents which are thought to have a central sympatho-inhibitory action.

摘要

在麻醉大鼠的后爪脚垫中诱发交感胆碱能发汗运动系统的皮肤电反应(EDR)。反应最强烈的中枢神经系统位点位于下丘脑后部区域的尾侧。通过对去传入的胫神经进行电刺激来诱发外周诱发反应。这些诱发的EDR的幅度随时间稳定,并且中枢和外周诱发的反应均与频率相关。阿托品(200微克/千克)抑制外周和中枢刺激诱发的EDR,而六甲铵(20毫克/千克)仅抑制中枢EDR。可乐定对外周诱发的EDR没有影响,但对中枢诱发的EDR产生显著的剂量依赖性抑制作用;育亨宾(0.75毫克/千克)可部分拮抗这种作用。有人提出,大鼠是在研究被认为具有中枢交感抑制作用的肾上腺素能药物时使用发汗运动系统的合适物种。

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