Correlation between inhibitions of morphine withdrawal and nitric-oxide synthase by agmatine.

J Li, X Li, G Pei, B Y Qin
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Abstract

Aim: To study correlation between inhibitions of naloxone-precipitated withdrawal jumps and nitric-oxide synthase (NOS) activity by agmatine.

Methods: NOS activities in mouse brain were measured by determination of concentration of [3H]citrulline, the product of [3H]arginine.

Results: Agmatine inhibited NOS activity in naive and morphine-dependent mouse cerebellum, forebrain, and thalamus in substrate-competitive manner in vitro. Naloxone induced withdrawal jumps and an increase in NOS activity in cerebellum, forebrain, and thalamus of abstinent mice. Pretreatment of mice with morphine plus agmatine inhibited the effect of naloxone to precipitate withdrawal jumps and increase in NOS activity. The effect of agmatine was blocked by idazoxan.

Conclusion: The inhibitory effect of agmatine on naloxone-precipitated withdrawal jumps is related to its inhibition of NOS activity by substrate competitive manner and activation of imidazoline receptors.

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胍丁胺抑制吗啡戒断与一氧化氮合酶的关系。
目的:研究胍丁氨酸抑制纳洛酮沉淀戒断跳跃与一氧化氮合酶(NOS)活性的关系。方法:通过测定[3H]精氨酸产物[3H]瓜氨酸浓度,测定小鼠脑内NOS活性。结果:胍丁胺在体外以底物竞争方式抑制吗啡依赖小鼠小脑、前脑和丘脑的NOS活性。纳洛酮引起戒断小鼠小脑、前脑和丘脑NOS活性增加。吗啡加胍丁胺预处理小鼠,抑制纳洛酮沉淀戒断跳跃和NOS活性增加的作用。咪唑嗪阻断了胍丁氨酸的作用。结论:胍丁胺对纳洛酮沉淀戒断跳跃的抑制作用与其通过底物竞争方式抑制NOS活性和激活咪唑啉受体有关。
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