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金刚烷胺震颤,一种5-羟色胺介导的反应?

Amantadin e tremor, a 5-hydroxytryptamine-mediated response?

作者信息

Cox B, Tha S J

出版信息

Eur J Pharmacol. 1975 Feb;30(2):344-51. doi: 10.1016/0014-2999(75)90119-3.

Abstract

Amantadine-induced tremor has been investigated using mice. Experiments with, mebanazine, reserpine, diethyldithiocarbamate, and p-chlorophenylalanine suggest that the tremorgenic action of amantadine is influenced by a balance between three putative central nervous system (CNS) transmitters: noradrenaline, dopamine and 5-hydroxytryptamine (5-HT). Drugs which reduce the concentration of the catecholamines in brain increase amantadine induced tremor. p-Chlorophenylalanine, which specifically depletes brain 5-HT, antagonises amantadine-induced tremor. An ED50 (tremor) dose of amantadine decreases the concentration of 5-hydroxy-indoleacetic acid (5-HIAA) in rat brain, particularly when this elevated due to pretreatment with 5-hydroxytryptophan. Neither inhibition of monoamine oxidase nor reduction of 5-HT-reuptake appear to be responsible for this decrease. Experiments on rat fundus suggest that amantadine increased the sensitivity of receptors to 5-HT. A similar mechanism of action in the CNS could explain both the tremor and the decrease in brain 5-HIAA. The possible relevance of these findings is discussed with respect to the known anti-Parkinson action of amantadine.

摘要

已经利用小鼠对金刚烷胺诱发的震颤进行了研究。使用美加明、利血平、二乙基二硫代氨基甲酸盐和对氯苯丙氨酸进行的实验表明,金刚烷胺的致颤作用受三种假定的中枢神经系统(CNS)递质之间平衡的影响:去甲肾上腺素、多巴胺和5-羟色胺(5-HT)。降低脑中儿茶酚胺浓度的药物会增加金刚烷胺诱发的震颤。特异性耗尽脑5-HT的对氯苯丙氨酸可拮抗金刚烷胺诱发的震颤。金刚烷胺的半数有效剂量(致颤)会降低大鼠脑中5-羟吲哚乙酸(5-HIAA)的浓度,尤其是在因用5-羟色氨酸预处理而升高时。单胺氧化酶的抑制和5-HT再摄取的减少似乎都不是导致这种降低的原因。对大鼠眼底的实验表明,金刚烷胺增加了受体对5-HT的敏感性。中枢神经系统中类似的作用机制可以解释震颤和脑5-HIAA的降低。就金刚烷胺已知的抗帕金森作用而言,讨论了这些发现的可能相关性。

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