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肝脏糖异生:高蛋白喂养大鼠应对餐后氨基酸过量的一条途径?

Liver glyconeogenesis: a pathway to cope with postprandial amino acid excess in high-protein fed rats?

作者信息

Azzout-Marniche Dalila, Gaudichon Claire, Blouet Clémence, Bos Cécile, Mathé Véronique, Huneau Jean-François, Tomé Daniel

机构信息

INRA, AgroParisTech, UMR914 Nutrition Physiology and Ingestive Behavior, 16 rue Claude Bernard, Paris, F75005, France.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2007 Apr;292(4):R1400-7. doi: 10.1152/ajpregu.00566.2006. Epub 2006 Dec 7.

Abstract

This paper provides molecular evidence for a liver glyconeogenic pathway, that is, a concomitant activation of hepatic gluconeogenesis and glycogenesis, which could participate in the mechanisms that cope with amino acid excess in high-protein (HP) fed rats. This evidence is based on the concomitant upregulation of phosphoenolpyruvate carboxykinase (PEPCK) gene expression, downregulation of glucose 6-phosphatase catalytic subunit (G6PC1) gene expression, an absence of glucose release from isolated hepatocytes and restored hepatic glycogen stores in the fed state in HP fed rats. These effects are mainly due to the ability of high physiological concentrations of portal blood amino acids to counteract glucagon-induced liver G6PC1 but not PEPCK gene expression. These results agree with the idea that the metabolic pathway involved in glycogen synthesis is dependent upon the pattern of nutrient availability. This nonoxidative glyconeogenic disposal pathway of gluconeogenic substrates copes with amino excess and participates in adjusting both amino acid and glucose homeostasis. In addition, the pattern of PEPCK and G6PC1 gene expression provides evidence that neither the kidney nor the small intestine participated in gluconeogenic glucose production under our experimental conditions. Moreover, the main glucose-6-phosphatase (G6Pase) isoform expressed in the small intestine is the ubiquitous isoform of G6Pase (G6PC3) rather than the G6PC1 isoform expressed in gluconeogenic organs.

摘要

本文提供了肝脏糖异生途径的分子证据,即肝脏糖异生和糖原生成的同时激活,这可能参与了高蛋白(HP)喂养大鼠应对氨基酸过量的机制。该证据基于磷酸烯醇式丙酮酸羧激酶(PEPCK)基因表达的同时上调、葡萄糖6-磷酸酶催化亚基(G6PC1)基因表达的下调、分离的肝细胞中无葡萄糖释放以及HP喂养大鼠在进食状态下肝脏糖原储备的恢复。这些效应主要归因于高生理浓度的门静脉血氨基酸能够抵消胰高血糖素诱导的肝脏G6PC1基因表达,但不能抵消PEPCK基因表达。这些结果与糖原合成所涉及的代谢途径取决于营养物质供应模式的观点一致。这种糖异生底物的非氧化糖异生处置途径应对氨基酸过量,并参与调节氨基酸和葡萄糖的稳态。此外,PEPCK和G6PC1基因表达模式提供了证据,表明在我们的实验条件下,肾脏和小肠均未参与糖异生葡萄糖的产生。此外,小肠中表达的主要葡萄糖-6-磷酸酶(G6Pase)同工型是G6Pase的普遍存在的同工型(G6PC3),而不是糖异生器官中表达的G6PC1同工型。

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