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二甲双胍对大鼠小肠中SGLT1、GLUT2和GLUT5己糖转运蛋白基因表达的影响。

Effect of metformin on SGLT1, GLUT2, and GLUT5 hexose transporter gene expression in small intestine from rats.

作者信息

Lenzen S, Lortz S, Tiedge M

机构信息

nstitute of Clinical Biochemistry, Hannover Medical School, Hannover, Germany.

出版信息

Biochem Pharmacol. 1996 Apr 12;51(7):893-6. doi: 10.1016/0006-2952(95)02243-0.

Abstract

The effect of the antihyperglycaemic agent metformin was studied on gene expression of the energy-dependent sodium-hexose cotransporter (SGLT1) and the facilitative hexose transporters GLUT2 and GLUT5 in rat intestine. Metformin treatment (125 mg/kg body wt. twice daily for a period of 3 days) significantly increased SGLT1 gene expression in duodenum and jejunum. GLUT5 gene expression was increased by metformin treatment only in the jejunum. Gene expression of GLUT2 in the intestine was not significantly affected by metformin treatment. This increase in transporter gene expression offers the potential for increases in hexose uptake at the brush border membrane, and may compensate for other effects of the drug that have been suggested to decrease glucose uptake by SGLT1, as well as for metformin stimulation of glucose utilization by the intestinal mucosa.

摘要

研究了抗高血糖药物二甲双胍对大鼠肠道中能量依赖性钠-己糖共转运蛋白(SGLT1)以及易化性己糖转运蛋白GLUT2和GLUT5基因表达的影响。二甲双胍治疗(125mg/kg体重,每日两次,持续3天)显著增加了十二指肠和空肠中SGLT1的基因表达。二甲双胍治疗仅使空肠中的GLUT5基因表达增加。二甲双胍治疗对肠道中GLUT2的基因表达没有显著影响。转运蛋白基因表达的这种增加有可能提高刷状缘膜处己糖的摄取,并可能补偿该药物其他已表明会降低SGLT1介导的葡萄糖摄取的作用,以及二甲双胍对肠黏膜葡萄糖利用的刺激作用。

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