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一种由心脏磷酸化酶激酶缺乏引起的新型糖原贮积病。

A new type of glycogen storage disease caused by deficiency of cardiac phosphorylase kinase.

作者信息

Mizuta K, Hashimoto E, Tsutou A, Eishi Y, Takemura T, Narisawa K, Yamamura H

出版信息

Biochem Biophys Res Commun. 1984 Mar 15;119(2):582-7. doi: 10.1016/s0006-291x(84)80288-0.

Abstract

A five-month-old Japanese boy was found to have marked glycogen accumulation only in the heart. A survey of enzymes revealed normal activities of phosphorylase, cyclic AMP-dependent protein kinase, acid maltase and amylo-1,6-glucosidase. However, the heart had capacity of activating neither rabbit muscle phosphorylase b nor endogenous phosphorylase b, which was converted to active form only when supplemented rabbit muscle phosphorylase kinase. In contrast to the heart, activities of phosphorylase kinase were found within normal levels in other organ tissues so far tested. These findings indicate that the present case of the cardiac glycogenosis is caused by deficiency of cardiac phosphorylase kinase.

摘要

一名五个月大的日本男婴被发现仅在心脏中有明显的糖原积累。对酶的检测显示,磷酸化酶、环磷酸腺苷依赖性蛋白激酶、酸性麦芽糖酶和淀粉-1,6-葡萄糖苷酶的活性正常。然而,心脏既没有激活兔肌肉磷酸化酶b的能力,也没有激活内源性磷酸化酶b的能力,只有在添加兔肌肉磷酸化酶激酶时,内源性磷酸化酶b才会转化为活性形式。与心脏不同,在迄今为止检测的其他器官组织中,磷酸化酶激酶的活性处于正常水平。这些发现表明,目前的心脏糖原贮积症病例是由心脏磷酸化酶激酶缺乏引起的。

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