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可乐定对发育中大鼠的运动效应及其与α-氟哌噻吨或氟哌啶醇的相互作用。

The locomotor effect of clonidine and its interaction with alpha-flupenthixol or haloperidol in the developing rat.

作者信息

Nomura Y

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1980 Aug;313(1):33-7. doi: 10.1007/BF00505802.

Abstract

The interaction of clonidine with alpha-flupenthixol and haloperidol on the locomotion was investigation in the rat during postnatal development. A subcutaneous injection of clonidine 0.039--3.9 mu mol/kg produced a marked hypermotility in infant animals between day 1 and day 7 but hypomotility in animals older than 20 days. Pretreatment with alpha-flupenthixol and haloperidol significantly reduced clonidine-hypermotility in infants. In adult rats, clonidine-hypomotility were increased by a preceding administration of alpha-flupenthixol. It is suggested that intact function of both alpha-adrenoceptors and dopamine receptors is involved in the control of locomotor activity in developing rats and that there is the complex interaction of noradrenergic and dopaminergic system in the control of locomotor activity.

摘要

在出生后发育过程中,对大鼠进行了可乐定与α-氟哌噻吨及氟哌啶醇对运动的相互作用研究。皮下注射0.039 - 3.9μmol/kg的可乐定,在出生后第1天至第7天的幼龄动物中产生明显的运动亢进,但在20日龄以上的动物中则产生运动减退。用α-氟哌噻吨和氟哌啶醇预处理可显著降低幼龄动物的可乐定诱导的运动亢进。在成年大鼠中,预先给予α-氟哌噻吨可增强可乐定诱导的运动减退。提示α-肾上腺素能受体和多巴胺受体的完整功能均参与发育中大鼠运动活动的控制,并且在运动活动的控制中去甲肾上腺素能和多巴胺能系统存在复杂的相互作用。

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