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大鼠电刺激自身兴奋和药物诱导震颤中的中枢胆碱能机制。

Central cholinergic mechanisms in electrical self-stimulation and in drug-induced tremor in rats.

作者信息

Wishart T B, Herberg L J

出版信息

Pharmacol Biochem Behav. 1979 Dec;11(6):625-9. doi: 10.1016/0091-3057(79)90253-3.

Abstract

Oxotremorine, a specific stimulant of central muscarinic acetylcholine receptors, inhibited lateral hypothalamic self-stimulation at a dose-level less than one-tenth of that necessary to produce body tremor. Tremor induced by oxotremorine (0.5 mg/kg) was inhibited by pretreatment with hyoscine (scopolamine) (0.3 mg/kg) or propranolol (20 mg/kg) but not by methylhyoscine (0.3 mg/kg) or apomorphine (0.3 mg/kg). Inhibition of self-stimulation by oxotremorine (.03 mg/kg) was prevented by hyoscine (0.3 mg/kg) but not by any other of the drugs tested and thus constitutes a uniquely specific in vivo model for assessing central antimuscarinic activity. The results confirm the presence of centrally situated ACh receptors eleciting tremor and inhibiting self-stimulation but provide no evidence of an effect on tremor by central adrenergic beta-receptors.

摘要

氧化震颤素是一种中枢毒蕈碱型乙酰胆碱受体的特异性兴奋剂,它抑制下丘脑外侧的自我刺激,其剂量水平低于产生身体震颤所需剂量的十分之一。氧化震颤素(0.5毫克/千克)诱发的震颤可被预先给予的东莨菪碱(0.3毫克/千克)或普萘洛尔(20毫克/千克)抑制,但不能被甲东莨菪碱(0.3毫克/千克)或阿扑吗啡(0.3毫克/千克)抑制。氧化震颤素(0.03毫克/千克)对自我刺激的抑制作用可被东莨菪碱(0.3毫克/千克)阻止,但不能被所测试的任何其他药物阻止,因此构成了一种独特的用于评估中枢抗毒蕈碱活性的体内模型。结果证实存在位于中枢的引发震颤并抑制自我刺激的乙酰胆碱受体,但没有提供中枢肾上腺素能β受体对震颤有影响的证据。

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