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糖异生紊乱。

Disorders of gluconeogenesis.

作者信息

van den Berghe G

机构信息

Laboratory of Physiological Chemistry, International Institute of Cellular and Molecular Pathology, Brussels, Belgium.

出版信息

J Inherit Metab Dis. 1996;19(4):470-7. doi: 10.1007/BF01799108.

Abstract

Gluconeogenesis, or the formation of glucose from mainly lactate/ pyruvate, glycerol and alanine, plays an essential role in the maintenance of normoglycaemia during fasting. Inborn deficiencies are known of each of the four enzymes of the glycolytic-gluconeogenic pathway that ensure a unidirectional flux from pyruvate to glucose: pyruvate carboxylase, phosphoenolpyruvate carboxykinase, fructose-1,6-bisphosphatase, and glucose-6-phosphatase. In this paper, the clinical picture, pathophysiology, diagnostic tests, genetics, treatment and prognosis of the deficiencies of fructose-1,6-bisphosphatase and phosphoenolpyruvate carboxykinase are reviewed.

摘要

糖异生作用,即主要由乳酸/丙酮酸、甘油和丙氨酸生成葡萄糖的过程,在禁食期间维持血糖正常方面起着至关重要的作用。糖酵解-糖异生途径中的四种酶各自都存在先天性缺陷,这些酶确保了从丙酮酸到葡萄糖的单向通量,它们分别是丙酮酸羧化酶、磷酸烯醇式丙酮酸羧激酶、果糖-1,6-二磷酸酶和葡萄糖-6-磷酸酶。本文对果糖-1,6-二磷酸酶和磷酸烯醇式丙酮酸羧激酶缺乏症的临床表现、病理生理学、诊断测试、遗传学、治疗及预后进行了综述。

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