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组胺及组胺能药物对平滑肌制剂中去甲肾上腺素摄取的作用。

Role of histamine and histaminergic agents on noradrenaline uptake in smooth muscle preparations.

作者信息

Zamfirova R, Todorov S, Konstantinova E

机构信息

Institute of Physiology, Bulgarian Academy of Science, Sofia.

出版信息

Methods Find Exp Clin Pharmacol. 1994 Jan-Feb;16(1):15-9.

PMID:8164470
Abstract

It has been shown that adrenergic neurotransmission in different tissues can be modified by histamine (HIST) but the mechanisms of this action have still not been fully clarified. This study aimed to demonstrate the possible involvement of H-receptor subtypes in the realization of histamine inhibitory effects on smooth muscle tissues. HIST, 2-(2-aminoethyl)thiazole (AET) and dimaprit (DMP) exerted a similar inhibition of noradrenaline (NA)-uptake1 in rat vas deferens and rabbit ear artery. After H1-blockade with mepyramine (MEP), HIST and DMP did not change the uptake1 in rat vas deferens and decreased NA neuronal accumulation in rabbit ear artery. The H2-blockade with ranitidine (RAN) did not affect HIST- and AET-induced inhibition of NA-uptake1 in rat vas deferens and completely abolished it in rabbit ear artery. These data suggest that different H-receptor subtypes might be involved in HIST inhibitory action on NA neuronal uptake in both tissues. It appears, however, that the inhibition of NA uptake1 plays only a minor role in the effects of HIST on smooth muscle contractions.

摘要

已表明组胺(HIST)可改变不同组织中的肾上腺素能神经传递,但其作用机制仍未完全阐明。本研究旨在证明H受体亚型可能参与组胺对平滑肌组织的抑制作用的实现过程。组胺、2-(2-氨基乙基)噻唑(AET)和二甲双胍(DMP)对大鼠输精管和兔耳动脉中的去甲肾上腺素(NA)摄取1具有相似的抑制作用。用美吡拉敏(MEP)阻断H1后,组胺和二甲双胍并未改变大鼠输精管中的摄取1,却降低了兔耳动脉中NA的神经元蓄积。用雷尼替丁(RAN)阻断H2对组胺和AET诱导的大鼠输精管中NA摄取1的抑制作用没有影响,但在兔耳动脉中则完全消除了这种抑制作用。这些数据表明,不同的H受体亚型可能参与了组胺对两种组织中NA神经元摄取的抑制作用。然而,NA摄取1的抑制似乎在组胺对平滑肌收缩的影响中仅起次要作用。

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