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一氧化氮合酶抑制剂L-NA对胆汁淤积小鼠模型中纳洛酮诱发的戒断症状的抑制作用。

Inhibition by L-NA, a nitric oxide synthase inhibitor, of naloxone-precipitated withdrawal signs in a mouse model of cholestasis.

作者信息

Ghafourifar P, Dehpour A R, Akbarloo N

机构信息

Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Iran.

出版信息

Life Sci. 1997;60(19):PL 265-70. doi: 10.1016/s0024-3205(97)00115-x.

Abstract

Following the naloxone administration in bile duct resected animals, striking opioid withdrawal signs are observed due to increased opioidergic tone. Pretreatment of animals with L-nitro arginine, a nitric oxide synthase inhibitor, reduces the naloxone-precipitated withdrawal signs as well as increase the antinociception. The results of this study support evidence for the involvement of the L-arg-nitric oxide pathway in opioidergic-dependent manifestation of cholestasis in an animal model.

摘要

在对胆管切除的动物给予纳洛酮后,由于阿片能张力增加,观察到明显的阿片戒断症状。用一氧化氮合酶抑制剂L-硝基精氨酸对动物进行预处理,可减少纳洛酮诱发的戒断症状,并增强抗伤害感受作用。本研究结果支持L-精氨酸-一氧化氮途径参与动物模型中胆汁淤积的阿片能依赖性表现的证据。

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