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体内甲状腺素治疗对大鼠脂肪细胞中胰岛素受体、葡萄糖转运及葡萄糖转运蛋白4的影响。

The effect of in vivo thyroxine treatment on insulin receptors, glucose transport and GLUT4 in rat adipocytes.

作者信息

Fickova M, Zorad S, Macho L

机构信息

Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia.

出版信息

Horm Metab Res. 1997 Jan;29(1):16-9. doi: 10.1055/s-2007-978973.

Abstract

Daily i.p. administration of thyroxine (T4; 50 micrograms/100 g BW) to adult male rats for one week doubled the thyroxinemia and induced significant augmentation of glycemia and insulinemia. Hyperthyroxinemia was also manifested by significant elevation of liver malic enzyme activity and by the presence of smaller fat cells. Adipocytes of T4 treated rats displayed significantly lower density of insulin receptors, decreased insulin stimulatory effect on glucose transport and less glucose transporter (GLUT4) protein in plasma membranes after insulin stimulation as those of controls. These results indicate a deleterious effect of hyperthyroxinemia on insulin controlled glucose metabolism in fat cells.

摘要

对成年雄性大鼠每日腹腔注射甲状腺素(T4;50微克/100克体重),持续一周,可使甲状腺素血症翻倍,并导致血糖和胰岛素血症显著升高。甲状腺素血症还表现为肝脏苹果酸酶活性显著升高以及脂肪细胞变小。与对照组相比,经T4处理的大鼠脂肪细胞显示胰岛素受体密度显著降低,胰岛素对葡萄糖转运的刺激作用减弱,胰岛素刺激后质膜中的葡萄糖转运蛋白(GLUT4)减少。这些结果表明甲状腺素血症对脂肪细胞中胰岛素控制的葡萄糖代谢具有有害作用。

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