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[儿茶酚胺在肝脑变性发病机制生化机制中的作用]

[Role of catecholamines in the biochemical mechanisms of the pathogenesis of hepatocerebral dystrophy].

作者信息

Barkhatova V P

出版信息

Zh Nevropatol Psikhiatr Im S S Korsakova. 1982;82(7):78-84.

PMID:7124230
Abstract

In 48 patients with hepatocerebral dystrophy the principal parameters of the catecholamine metabolism were examined. Pronounced changes characterized primarily by a considerable diminution of dopamine and noradrenaline excretion and an increase of the excretion of their immediate precursor, i.e. DOPA, were noted. On the basis of the data obtained it was assumed that the synthesis of these neurotransmitting catecholamines was depressed. In the course of treatment with d-penicillamine which is capable of mobilizing copper and stimulating its excretion from the body a statistically significant increase of the dopamine excretion (as compared with its initial level) was noted, and in patients with the graver rigid-arrhythmohyperkinetic form of the disease the excretion of not only dopamine, but also noradrenaline, was increased. It is supposed that the disturbances of catecholamine metabolism in hepatocerebral dystrophy have a complicated mechanism, and are associated with both the grave hepatic pathology and disturbances of copper metabolism. In this connection additional methods of treating that disease are offered. These methods influence catecholamine metabolism, and act primarily on extrapyramid motor, and also psychic disorders. The studies carried out by the author make a contribution to the existing concepts of the biochemical mechanisms of the hepatocerebral dystrophy pathogenesis, and expand the possibilities of treating the grave hereditary disease.

摘要

对48例肝脑变性患者的儿茶酚胺代谢主要参数进行了检测。发现了明显变化,主要表现为多巴胺和去甲肾上腺素排泄量显著减少,而其直接前体即多巴的排泄量增加。根据所获数据推测,这些神经递质儿茶酚胺的合成受到抑制。在用能够动员铜并促进其从体内排泄的d-青霉胺治疗过程中,发现多巴胺排泄量(与初始水平相比)有统计学意义的增加,而且在病情较重的强直-心律失常-运动增多型患者中,不仅多巴胺排泄量增加,去甲肾上腺素排泄量也增加。据推测,肝脑变性中儿茶酚胺代谢紊乱机制复杂,与严重的肝脏病变及铜代谢紊乱均有关。就此提出了该病的其他治疗方法。这些方法影响儿茶酚胺代谢,主要作用于锥体外系运动障碍以及精神障碍。作者所进行的研究对肝脑变性发病机制的生化机制现有概念有所贡献,并拓展了治疗这种严重遗传性疾病的可能性。

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