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假定神经递质在前列腺素E2对大鼠胃的中枢性抑酸作用中的作用

Role of putative neurotransmitters in the central gastric antisecretory effect of prostaglandin E2 in rats.

作者信息

Puurunen J

出版信息

Br J Pharmacol. 1985 May;85(1):213-21. doi: 10.1111/j.1476-5381.1985.tb08849.x.

Abstract

The role of putative neurotransmitters of the central nervous system in the central gastric antisecretory effect of prostaglandin E2 (PGE2) was investigated in pylorus-ligated rats. Pretreatment of the rats with an intracerebroventricular (i.c.v.) injection of 6-hydroxydopamine (6-OHDA) prevented the antisecretory effect of the i.c.v. administration of PGE2, whereas pretreatment with 5,6-dihydroxytryptamine (5,6-DHT) plus p-chlorophenylalanine (PCPA) had no effect. I.c.v.-administered phentolamine and idazoxan antagonized the inhibition of gastric secretion induced by i.c.v. PGE2, whereas prazosin, propranolol and sulpiride injected via the same route were ineffective. Diphenhydramine, cimetidine, naloxone and theophylline, all administered i.c.v., did not modify the antisecretory effect of i.c.v. PGE2. The results suggest that an activation of alpha 2-adrenoceptors in the brain is involved in the central gastric antisecretory effect of PGE2, whereas neither central 5-hydroxytryptamine receptors, alpha 1- or beta-adrenoceptors, D2-dopamine receptors, histamine or opioid receptors nor adenosine seem to play any role here.

摘要

在幽门结扎的大鼠中研究了中枢神经系统假定神经递质在前列腺素E2(PGE2)的中枢性胃泌酸抑制作用中的作用。给大鼠脑室内注射6-羟基多巴胺(6-OHDA)进行预处理,可防止脑室内注射PGE2的泌酸抑制作用,而用5,6-二羟基色胺(5,6-DHT)加对氯苯丙氨酸(PCPA)进行预处理则无作用。脑室内注射酚妥拉明和咪唑克生可拮抗脑室内注射PGE2引起的胃分泌抑制,而经相同途径注射的哌唑嗪、普萘洛尔和舒必利则无效。脑室内注射苯海拉明、西咪替丁、纳洛酮和茶碱均未改变脑室内注射PGE2的泌酸抑制作用。结果表明,脑中α2-肾上腺素能受体的激活参与了PGE2的中枢性胃泌酸抑制作用,而中枢5-羟色胺受体、α1-或β-肾上腺素能受体、D2-多巴胺受体、组胺或阿片受体以及腺苷在此似乎均不起任何作用。

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Central gastric antisecretory action of adenosine in the rat.腺苷对大鼠胃的中枢性抑酸作用。
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