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蛋白质诱导性高胰岛素血症低血糖症的分子机制。

Molecular mechanisms of protein induced hyperinsulinaemic hypoglycaemia.

机构信息

Suresh Chandran, Department of Neonatology, KK Women's and Children's Hospital, Singapore 229899, Singapore.

出版信息

World J Diabetes. 2014 Oct 15;5(5):666-77. doi: 10.4239/wjd.v5.i5.666.

Abstract

The interplay between glucose metabolism and that of the two other primary nutrient classes, amino acids and fatty acids is critical for regulated insulin secretion. Mitochondrial metabolism of glucose, amino acid and fatty acids generates metabolic coupling factors (such as ATP, NADPH, glutamate, long chain acyl-CoA and diacylglycerol) which trigger insulin secretion. The observation of protein induced hypoglycaemia in patients with mutations in GLUD1 gene, encoding the enzyme glutamate dehydrogenase (GDH) and HADH gene, encoding for the enzyme short-chain 3-hydroxyacyl-CoA dehydrogenase has provided new mechanistic insights into the regulation of insulin secretion by amino acid and fatty acid metabolism. Metabolic signals arising from amino acid and fatty acid metabolism converge on the enzyme GDH which integrates both signals from both pathways and controls insulin secretion. Hence GDH seems to play a pivotal role in regulating both amino acid and fatty acid metabolism.

摘要

葡萄糖代谢与另外两种主要营养素——氨基酸和脂肪酸——的相互作用对于调节胰岛素分泌至关重要。葡萄糖、氨基酸和脂肪酸的线粒体代谢产生代谢偶联因子(如 ATP、NADPH、谷氨酸、长链酰基辅酶 A 和二酰基甘油),这些因子触发胰岛素分泌。在 GLUD1 基因(编码谷氨酸脱氢酶 [GDH] 的酶)和 HADH 基因(编码短链 3-羟酰基辅酶 A 脱氢酶的酶)发生突变的患者中观察到的蛋白诱导性低血糖症,为氨基酸和脂肪酸代谢调节胰岛素分泌提供了新的机制见解。来自氨基酸和脂肪酸代谢的代谢信号集中在酶 GDH 上,该酶整合了两条途径的信号,并控制胰岛素分泌。因此,GDH 似乎在调节氨基酸和脂肪酸代谢方面发挥着关键作用。

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本文引用的文献

1
Neonatal hypoglycemia.新生儿低血糖症
Indian J Pediatr. 2014 Jan;81(1):58-65. doi: 10.1007/s12098-013-1135-3. Epub 2013 Aug 1.
3

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