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κ型阿片类物质对乙醇摄入的影响。

Involvement of kappa type opioids on ethanol drinking.

作者信息

Sandi C, Borrell J, Guaza C

机构信息

Cajal Institute, Department of Psychobiology, C.S.I.C., Madrid, Spain.

出版信息

Life Sci. 1988;42(10):1067-75. doi: 10.1016/0024-3205(88)90562-0.

Abstract

The effects of the administration of the kappa agonist dynorphin1-17 and/or the kappa antagonist MR-2266-BS on ethanol preference was investigated using a paradigm by which rats develop alcohol preference. Administration of dynorphin shortly before or after the conditioning session (forced ethanol exposure) failed to affect later ethanol preference. However, dynorphin treatment prior to the first choice session reduced ethanol preference during the three consecutive testing days. This effect was reversed by the simultaneous administration of the kappa antagonist MR-2266-BS. The results of the present study provide further support for evidence of the involvement of dynorphinergic systems on drinking behavior and suggest that kappa-type opioid mechanisms may be involved in the consumption and development of preference to ethanol in rats.

摘要

使用一种使大鼠产生酒精偏好的范式,研究了κ激动剂强啡肽1 - 17和/或κ拮抗剂MR - 2266 - BS给药对乙醇偏好的影响。在条件训练阶段(强迫乙醇暴露)之前或之后不久给予强啡肽,并未影响随后的乙醇偏好。然而,在第一次选择阶段之前进行强啡肽治疗,在连续三天的测试中降低了乙醇偏好。同时给予κ拮抗剂MR - 2266 - BS可逆转这种效应。本研究结果为强啡肽能系统参与饮酒行为的证据提供了进一步支持,并表明κ型阿片类机制可能参与大鼠对乙醇的消费和偏好形成。

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