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咪唑诱导大鼠颤抖的拮抗作用:一种预测抗运动障碍活性的行为学工具?

Antagonism of imidazole-induced shaking in the rat: a behavioural tool predictive of antidyskinetic activity?

作者信息

Ferrari F, Ferrari P, Baggio G, Mangiafico V

出版信息

Arch Int Pharmacodyn Ther. 1986 Oct;283(2):209-21.

PMID:3789884
Abstract

In rats the intraperitoneal injection of imidazole (IMID) induced shaking behaviour, the effect appearing to be age- and sex-linked; younger animals responded less vigorously than older animals, while females always exhibited a significantly weaker response than males of the same age. After ovariectomy, however, the number of shakes of the two sexes was very similar. A number of drugs were examined for their antagonism of this highly reproducible syndrome. IMID-shakes were antagonized by reserpine, clonidine, high doses of B-HT 920, propranolol, haloperidol, morphine and diazepam, were not affected by apomorphine, (+)3-PPP, physostigmine, naloxone or methysergide, and were potentiated by sulpiride and scopolamine. The results are considered in the light of the possible neurochemical mechanisms underlying the IMID-syndrome; the suggested usefulness of this test for the study of human dyskinetic movements is disputed.

摘要

在大鼠中,腹腔注射咪唑(IMID)会诱发颤抖行为,这种效应似乎与年龄和性别有关;年幼动物的反应不如年长动物强烈,而雌性动物的反应总是比同龄雄性动物明显较弱。然而,卵巢切除术后,两性的颤抖次数非常相似。研究了多种药物对这种高度可重复综合征的拮抗作用。利血平、可乐定、高剂量的B-HT 920、普萘洛尔、氟哌啶醇、吗啡和地西泮可拮抗IMID诱发的颤抖,阿扑吗啡、(+)3-PPP、毒扁豆碱、纳洛酮或甲基麦角新碱对其无影响,而舒必利和东莨菪碱可增强这种颤抖。根据IMID综合征潜在的可能神经化学机制对结果进行了分析;有人对该试验在研究人类运动障碍方面的潜在用途提出了质疑。

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