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腺苷、腺嘌呤核苷酸和吗啡对胆碱能神经乙酰胆碱释放的抑制作用:茶碱的拮抗作用。

Inhibition of acetylcholine release from cholinergic nerves by adenosine, adenine nucleotides and morphine: antagonism by theophylline.

作者信息

Sawynok J, Jhamandas K H

出版信息

J Pharmacol Exp Ther. 1976 May;197(2):379-90.

PMID:1271286
Abstract

Adenosine and adenine nucleotides [adenosine-5'-monophosphate, adenosine-5'-diphosphate, adenosine triphosphate (ATP), cyclic adenosine 3',5'-monophosphate (dbcAMP)], but not (cAMP) and dibutyryl cyclic adenosine 3',5'-monosphosphate (dbcAMP)], but not adenine or inosine, inhibited the twitch response of the electrically stimulated guinea-pig myenteric plexus-longitudinal muscle preparation. With each agent except dbcAMP, inhibition was manifest muscle preparation. With each agent except dbcAMP, inhibition was manifest from 1 to 500 muM was maximal within 1 minute. For dbcAMP, higher concentrations were required (10-fold increase) and inhibition was maximal after 20 to 30 minutes. Theophylline (0.05-0.5 mM) both reversed and prevented the inhibition produced by each of these agents. In higher concentrations (greater than 1 mM), theophylline itself depressed the twitch response. Neither propranolol nor phenoxybenzamine altered theophylline-induced depression, whereas phenoxybenzamine did not alter adenosine-induced inhibition. Adenosine, ATP, cAMP and theophylline (0.25 mM) did not alter acetylcholine-induced contractions, whereas a higher concentration of theophylline (2.5 mM) inhibited contractions. Theophylline (up to 0.5 mM) did not antagonize epinephrine- or dopamine-induced inhibition of the twitch response, but did antagonize morphine-induced inhibition. These findings suggest that adenosine and related nucleotides act at a common receptor site at which theophylline acts as a competitive antagonist and that there is a link between morphine and adenine nucleotide action in this preparation.

摘要

腺苷及腺嘌呤核苷酸[5'-单磷酸腺苷、5'-二磷酸腺苷、三磷酸腺苷(ATP)、环磷腺苷3',5'-单磷酸(dbcAMP)],而非(cAMP)及二丁酰环磷腺苷3',5'-单磷酸(dbcAMP),也非腺嘌呤或肌苷,可抑制电刺激豚鼠肠肌丛-纵肌标本的抽搐反应。除dbcAMP外,每种试剂在1至500μM浓度时,1分钟内抑制作用即显现,且抑制作用在该浓度范围内达到最大。对于dbcAMP,需要更高浓度(增加10倍),且20至30分钟后抑制作用达到最大。茶碱(0.05 - 0.5 mM)可逆转并预防这些试剂所产生的抑制作用。在更高浓度(大于1 mM)时,茶碱自身会抑制抽搐反应。普萘洛尔和酚苄明均未改变茶碱引起的抑制作用,而酚苄明未改变腺苷引起的抑制作用。腺苷、ATP、cAMP及茶碱(0.25 mM)未改变乙酰胆碱引起的收缩,而更高浓度的茶碱(2.5 mM)则抑制收缩。茶碱(高达0.5 mM)未拮抗肾上腺素或多巴胺引起的抽搐反应抑制,但拮抗了吗啡引起的抑制。这些发现表明,腺苷及相关核苷酸作用于一个共同的受体位点,茶碱在该位点作为竞争性拮抗剂发挥作用,且在该标本中吗啡与腺嘌呤核苷酸的作用之间存在联系。

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