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肠道在控制葡萄糖稳态中的新功能。

The new functions of the gut in the control of glucose homeostasis.

作者信息

Mithieux Gilles

机构信息

INSERM, U449, Lyon F-69372, France.

出版信息

Curr Opin Clin Nutr Metab Care. 2005 Jul;8(4):445-9. doi: 10.1097/01.mco.0000172587.17385.aa.

DOI:10.1097/01.mco.0000172587.17385.aa
PMID:15930972
Abstract

PURPOSE OF REVIEW

It has become clear during the past few years that the intestine is more than a digestive tract. In addition to its role as a subtle endocrine organ, its participation in endogenous glucose production, a property so far believed to be restricted to the liver and kidney, has been emphasized.

RECENT FINDINGS

The role of the gut in the regulation of glucose homeostasis has received further experimental accreditation from both animal and human studies. In relation to the molecular mechanisms of control of glucose production the potential regulatory role of glutaminase and glycerokinase has been suggested from studies of fasting, and the transcription of the glucose-6 phosphatase gene has been specified in an intestinal context. Furthermore, two newly described metabolic pathways accounting for the transepithelial transport of glucose have received further support: from the intestinal lumen to inside the enterocyte, involving a translocation of the glucose transporter Glut2 to the apical membrane, and from inside the enterocyte into the blood, involving glucose 6-phosphatase and independent of Glut2.

SUMMARY

The new knowledge regarding the control of glucose, glutamine, and glycerol metabolisms in the small intestine should be of interest to those who care for diabetic or septic patients, or are involved in nutrition research in humans. They should also be of importance in the knowledge of inherited genetic deficiencies, such as glycogen storage disease type 1 (Von Gierke disease) and the Fanconi-Bickel and glucose-galactose malabsorption syndromes.

摘要

综述目的

在过去几年中,肠道已不仅仅被视为一个消化道这一点变得愈发清晰。除了作为一个精细的内分泌器官发挥作用外,其在内源性葡萄糖生成中的参与也受到了关注,而这一特性此前一直被认为仅限于肝脏和肾脏。

最新发现

肠道在葡萄糖稳态调节中的作用已从动物和人体研究中获得了更多实验证据。关于葡萄糖生成控制的分子机制,禁食研究提示了谷氨酰胺酶和甘油激酶的潜在调节作用,并明确了葡萄糖 - 6 - 磷酸酶基因在肠道环境中的转录情况。此外,两种新描述的负责葡萄糖跨上皮转运的代谢途径也得到了更多支持:从肠腔到肠上皮细胞内,涉及葡萄糖转运蛋白Glut2向顶端膜的转位;从肠上皮细胞内到血液中,涉及葡萄糖6 - 磷酸酶且不依赖于Glut2。

总结

关于小肠中葡萄糖、谷氨酰胺和甘油代谢控制的新知识,对于关注糖尿病或脓毒症患者的人员,以及从事人类营养研究的人员来说应是有意义的。它们在诸如1型糖原贮积病(冯·吉尔克病)、范科尼 - 比克勒综合征和葡萄糖 - 半乳糖吸收不良综合征等遗传性基因缺陷的认识方面也应具有重要意义。

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