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去甲肾上腺素能受体阻断剂对大鼠脑内5-羟色胺代谢的影响。

The effect of noradrenergic receptor blocking agents on 5-hydroxytryptamine turnover in the brain of rats.

作者信息

Zebrowska-Lupina I

出版信息

Pol J Pharmacol Pharm. 1976 May-Jun;28(4):341-7.

PMID:135973
Abstract

Phenoxybenzamine (PB), phentolamine (PT) and aceperone (AC) in doses of 25 and 50 mg/kg increased cerebral noradrenaline (NA) turnover so these doses were regarded as blocking brain NA receptors. PB (50 mg/kg), PT (50 mg/kg) and AC (25 and 50 mg/kg) accelerated also the turnover of brain 5-HT. PT in a dose of 25 mg/kg counteracted deceleration of 5-HT turnover induced by clonidine but not by quipazine. Almost the same extent of decrease in 5-HIAA concentration after quipazine was observed in controls as in the rats pretreated with NA blockers in a dose of 25 mg/kg. On the contrary PT given in a dose of 50 mg/kg antagonized significantly the effect of quipazine. The results indicate that NA blockig agents given in lower doses do not affect the 5-HT system, however after higher doses such effect is possible.

摘要

以25毫克/千克和50毫克/千克的剂量给予苯氧苄胺(PB)、酚妥拉明(PT)和阿塞哌隆(AC)可增加脑内去甲肾上腺素(NA)的周转率,因此这些剂量被视为阻断脑内NA受体。PB(50毫克/千克)、PT(50毫克/千克)和AC(25毫克/千克和50毫克/千克)也加速了脑内5-羟色胺(5-HT)的周转率。25毫克/千克剂量的PT抵消了可乐定而非喹哌嗪引起的5-HT周转率减慢。在对照组中观察到的喹哌嗪后5-羟吲哚乙酸(5-HIAA)浓度降低程度与用25毫克/千克剂量的NA阻断剂预处理的大鼠中观察到的几乎相同。相反,50毫克/千克剂量的PT显著拮抗了喹哌嗪的作用。结果表明,较低剂量的NA阻断剂不影响5-HT系统,然而,在较高剂量后可能会有这种影响。

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