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单独或联合使用RO 15 - 4513和吲哚美辛进行预处理或后处理对乙醇的拮抗作用。

Antagonism of ethanol by pretreatment or posttreatment with RO 15-4513 and indomethacin alone or in combination.

作者信息

Elmer G I, George F R

机构信息

Southwest Institute on Drug and Alcohol Studies, Albuquerque, New Mexico 87190-3991, USA.

出版信息

Alcohol Clin Exp Res. 1995 Apr;19(2):490-5. doi: 10.1111/j.1530-0277.1995.tb01536.x.

Abstract

RO 15-4513, an inverse agonist at the GABA/benzodiazepine receptor Cl- channel complex, antagonizes multiple effects of ethanol. Prostaglandin synthesis inhibitors, such as indomethacin, also antagonize several effects of alcohols. However, prostaglandin synthesis inhibitors and RO 15-4513 each provide only partial antagonism of ethanol, typically seen as a dose-related effect with a maximum efficacy of approximately 50%. The purpose of this study was to: (1) compare the relative efficacy of these compounds for antagonizing ethanol; (2) compare the effectiveness of preethanol treatment versus postethanol treatment with each drug; and (3) compare the effect of RO 15-4513 and indomethacin in combination with the effects of each drug alone. The results show that indomethacin significantly decreased duration of loss of the righting reflex when administered either pre- or postethanol. Conversely, RO 15-4513 decreased duration of loss of the righting reflex only when given preethanol. When coadministered, RO 15-4513 and indomethacin did not show additive or synergistic effects. Compounds from these two drugs classes should continue to prove useful in elucidating ethanol's mechanisms of action.

摘要

RO 15 - 4513是一种γ-氨基丁酸/苯二氮䓬受体氯离子通道复合物的反向激动剂,可拮抗乙醇的多种作用。前列腺素合成抑制剂,如吲哚美辛,也能拮抗酒精的多种作用。然而,前列腺素合成抑制剂和RO 15 - 4513对乙醇的拮抗作用都只是部分性的,通常表现为一种剂量相关效应,最大效能约为50%。本研究的目的是:(1)比较这些化合物拮抗乙醇的相对效能;(2)比较每种药物在乙醇给药前治疗与乙醇给药后治疗的效果;(3)比较RO 15 - 4513和吲哚美辛联合使用的效果与每种药物单独使用的效果。结果显示,吲哚美辛在乙醇给药前或给药后使用时,均能显著缩短翻正反射消失的持续时间。相反,RO 15 - 4513只有在乙醇给药前使用时才会缩短翻正反射消失的持续时间。当两者合用时,RO 15 - 4513和吲哚美辛未显示出相加或协同作用。这两类药物的化合物在阐明乙醇的作用机制方面应会继续证明是有用的。

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