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大鼠体内吗啡和苯丙胺致瞳孔散大的自主神经机制

Autonomic mechanisms for morphine and amphetamine mydriasis in the rat.

作者信息

Klemfuss H, Adler M W

出版信息

J Pharmacol Exp Ther. 1986 Sep;238(3):788-93.

PMID:3018221
Abstract

Morphine sulfate and amphetamine sulfate dilate the pupil of the conscious, unrestrained rat. To examine the mechanisms underlying amphetamine and morphine mydriasis, the pupil diameter of freely moving rats was measured from photographs taken before and after these drugs were administered s.c., i.c.v. or by instillation into the eye. Some rats received monoamine antagonists, sympathetic denervation, or adrenalectomy before drug administration. The results indicate that both amphetamine and morphine mydriasis are primarily due to centrally mediated inhibition of parasympathetic outflow, although for both drugs there may be a sympathetic component. Pharmacological evidence indicates that the mydriatic effect of a low dose of amphetamine is mediated by actions on both alpha-1 and alpha-2 adrenergic receptors, whereas only alpha-2 adrenergic receptors are involved in morphine mydriasis.

摘要

硫酸吗啡和硫酸苯丙胺可使清醒、未受束缚的大鼠瞳孔散大。为研究苯丙胺和吗啡致瞳孔散大的机制,通过皮下注射、脑室内注射或滴眼给药后,从自由活动大鼠给药前后拍摄的照片测量瞳孔直径。一些大鼠在给药前接受了单胺拮抗剂、交感神经去神经支配或肾上腺切除术。结果表明,苯丙胺和吗啡所致瞳孔散大主要是由于中枢介导的副交感神经传出抑制,尽管两种药物可能都有交感神经成分。药理学证据表明,低剂量苯丙胺的散瞳作用是通过对α-1和α-2肾上腺素能受体的作用介导的,而吗啡散瞳仅涉及α-2肾上腺素能受体。

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