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慢性吗啡处理对大鼠心脏儿茶酚胺含量及机械反应的影响。

Effects of chronic morphine treatment on catecholamines content and mechanical response in the rat hearts.

作者信息

Rabadán J V, Milanés M V, Laorden M L

机构信息

Department of Physiology and Pharmacology, University School of Medicine, Murcia, Spain.

出版信息

J Pharmacol Exp Ther. 1997 Jan;280(1):32-7.

PMID:8996178
Abstract

Our investigation was aimed at elucidating if the chronic administration and withdrawal of a preferential mu-agonist, morphine, induce changes on the heart catecholaminergic neuronal activity. With this purpose the effects of morphine or naloxone (preferentially mu-antagonist) on noradrenaline, adrenaline or dopamine (DA) content and the mechanical response of the left atria were studied in chronically placebo- or morphine-treated rats (implanted s.c. with pellets for 7 days). In morphine-treated rats, a challenge dose of morphine (30 mg/kg i.p.) increased the auricular noradrenaline, adrenaline and DA content and decreased dihydroxy phenyl acetic acid/DA ratio; these changes were accompanied by a decrease in the force of contraction in the isolated left atria. No changes were observed in placebo-treated rats. The administration of naloxone (1 mg/kg s.c.) to morphine-treated animals induced a decrease on the auricular content of noradrenaline, adrenaline and DA and an increase in dihydroxy phenyl acetic acid/DA ratio. The study of the mechanical response to naloxone in the isolated left atria showed an enhancement in the force of contraction in preparations from morphine-treated rats, whereas in the placebo-pelleted rats naloxone induced a decrease in this parameter. These findings demonstrate that the heart of rats that had received chronic morphine-treatment exhibit excitatory reactions to naloxone-precipitated withdrawal and suggest that the changes observed in the heart by the chronic administration of morphine and after naloxone precipitated withdrawal are mostly mediated by the catecholaminergic system.

摘要

我们的研究旨在阐明长期给予并撤停一种选择性μ受体激动剂吗啡是否会引起心脏儿茶酚胺能神经元活动的变化。为此,我们研究了吗啡或纳洛酮(选择性μ受体拮抗剂)对长期接受安慰剂或吗啡治疗的大鼠(皮下植入药粒7天)的去甲肾上腺素、肾上腺素或多巴胺(DA)含量以及左心房机械反应的影响。在吗啡治疗的大鼠中,一剂激发剂量的吗啡(30毫克/千克腹腔注射)增加了心房去甲肾上腺素、肾上腺素和DA的含量,并降低了二羟基苯乙酸/DA比值;这些变化伴随着离体左心房收缩力的降低。在接受安慰剂治疗的大鼠中未观察到变化。对吗啡治疗的动物皮下注射纳洛酮(1毫克/千克)导致心房去甲肾上腺素、肾上腺素和DA含量降低,二羟基苯乙酸/DA比值升高。对离体左心房对纳洛酮的机械反应研究表明,吗啡治疗大鼠的制剂中收缩力增强,而在植入安慰剂药粒的大鼠中,纳洛酮导致该参数降低。这些发现表明,接受长期吗啡治疗的大鼠心脏对纳洛酮诱发的戒断表现出兴奋反应,并提示长期给予吗啡以及纳洛酮诱发戒断后在心脏中观察到的变化主要由儿茶酚胺能系统介导。

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