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毒蕈碱样和烟碱样对大鼠打哈欠和伸舌的影响。

Muscarinic and nicotinic effects on yawning and tongue protruding in the rat.

作者信息

Ushijima I, Yamada K, Inoue T, Tokunaga T, Furukawa T, Noda Y

出版信息

Pharmacol Biochem Behav. 1984 Aug;21(2):297-300. doi: 10.1016/0091-3057(84)90229-6.

Abstract

Physostigmine, an anticholinesterase agent, elicited yawning with a marked protrusion of the tongue and teeth chattering. Yawning and chattering were also observed after pilocarpine, a cholinergic agonist predominantly acting upon muscarinic receptors. Apomorphine at low doses (0.1-0.5 mg/kg), which preferentially activates presynaptic dopamine autoreceptors, elicited yawning, whereas at high doses (1-2 mg/kg) it produced stereotypy. Yawning induced by both cholinergic agonists and apomorphine was inhibited by scopolamine, a muscarinic receptor blocking agent, but not by methylscopolamine, a peripheral anticholinergic agent and mecamylamine, a nicotinic receptor blocking agent. Low dose (0.02 mg/kg) of haloperidol, which has been reported to block presynaptic dopamine autoreceptors, inhibited apomorphine-induced yawning but did not affect cholinergic agonist-induced yawning. Physostigmine-elicited tongue protruding was inhibited by mecamylamine. The results imply that yawning behavior is essentially associated with the stimulation of central muscarinic receptors, and that physostigmine also induces tongue protruding by activating the central nicotinic receptors.

摘要

毒扁豆碱,一种抗胆碱酯酶药,引发了打哈欠,并伴有明显的伸舌和牙齿打颤。毛果芸香碱,一种主要作用于毒蕈碱受体的胆碱能激动剂,给药后也观察到了打哈欠和打颤现象。低剂量(0.1 - 0.5毫克/千克)的阿扑吗啡优先激活突触前多巴胺自身受体,引发打哈欠,而高剂量(1 - 2毫克/千克)时则产生刻板行为。毒蕈碱受体阻断剂东莨菪碱可抑制胆碱能激动剂和阿扑吗啡诱导的打哈欠,但外周抗胆碱能药甲基东莨菪碱和烟碱受体阻断剂美加明则无此作用。据报道,低剂量(0.02毫克/千克)的氟哌啶醇可阻断突触前多巴胺自身受体,抑制阿扑吗啡诱导的打哈欠,但不影响胆碱能激动剂诱导的打哈欠。美加明可抑制毒扁豆碱引发的伸舌行为。结果表明,打哈欠行为本质上与中枢毒蕈碱受体的刺激有关,且毒扁豆碱还通过激活中枢烟碱受体诱导伸舌。

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