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局部用可乐定通过中枢神经系统作用产生散瞳。

Topical clonidine produces mydriasis by a central nervous system action.

作者信息

Koss M C

出版信息

Eur J Pharmacol. 1979 May 1;55(3):305-10. doi: 10.1016/0014-2999(79)90198-5.

Abstract

One drop of clonidine solution (0.125, 0.25 or 0.5%) was administered topically to one eye in cats anesthetized with pentobarbital in which the vagosympathetic nerves had been sectioned. Clonidine caused a simultaneous dose-related mydriasis in both eyes along with a decrease in heart rate. The peak effects were observed in about 20--30 min. Topical administration of clonidine (0.5%) produced no effect on the parasympathectomized, eserinized iris but did dilate the opposite pupil. Epinephrine (0.1--30 microgram, i.a.) produced equal pupillary dilation in both eyes. In addition, topical clonidine caused a dramatic decrease in postganglionic ciliary nerve activity. All of the effects of clonidine were antagonized by yohimbine (0.5 mg/kg, i.v.). These results demonstrate that topical administration of clonidine causes my driasis in the cat and that this effect is mediated totally by means of CNS inhibition of parasympathetic tone to the iris.

摘要

将一滴可乐定溶液(0.125%、0.25%或0.5%)局部滴入用戊巴比妥麻醉且已切断迷走交感神经的猫的一只眼睛。可乐定导致双眼同时出现与剂量相关的瞳孔散大以及心率下降。在约20 - 30分钟时观察到峰值效应。局部应用可乐定(0.5%)对已进行副交感神经切除、用毒扁豆碱处理过的虹膜无作用,但能使对侧瞳孔散大。肾上腺素(0.1 - 30微克,眼内注射)使双眼产生同等程度的瞳孔散大。此外,局部应用可乐定导致节后睫状神经活动显著降低。可乐定的所有效应均被育亨宾(0.5毫克/千克,静脉注射)拮抗。这些结果表明,局部应用可乐定可使猫出现瞳孔散大,且这种效应完全是通过中枢神经系统抑制虹膜的副交感神经张力介导的。

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