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用四氧嘧啶和链脲佐菌素诱导的糖尿病大鼠肝脏表皮生长因子受体表达降低。

Decreased expression of liver epidermal growth factor receptors in rats with alloxan and streptozotocin diabetes.

作者信息

Lev-Ran A, Hwang D L, Barseghian G

出版信息

Biochem Biophys Res Commun. 1986 May 29;137(1):258-62. doi: 10.1016/0006-291x(86)91204-0.

Abstract

Male rats (200 g) were rendered diabetic with one intraperitoneal injection of alloxan (150 mg/kg) or streptozotocin (60 mg/kg). In hyperglycemic animals within 3 hours after the injection, the binding of EGF to liver membranes decreased by 43-52%; the maximal drop was by 70% and persisted for the 20 days of the experiment. EGF receptors decreased in number with almost no changes in their affinity. Autophosphorylation of the receptors decreased parallel to the ligand binding. In animals that received lower doses and did not develop diabetes and in animals in whom diabetes was prevented by the injections of glucose (before alloxan) or nicotinamide (before streptozotocin) the binding of EGF to liver receptors remained normal. We conclude that the decreased expression of EGF receptors was caused by diabetes and not by the toxic effects of the diabetogenic compounds on the liver.

摘要

雄性大鼠(200克)通过腹腔注射一次四氧嘧啶(150毫克/千克)或链脲佐菌素(60毫克/千克)诱导糖尿病。注射后3小时内的高血糖动物中,表皮生长因子(EGF)与肝细胞膜的结合减少了43%-52%;最大降幅为70%,并在实验的20天内持续存在。EGF受体数量减少,其亲和力几乎没有变化。受体的自磷酸化与配体结合平行下降。在接受较低剂量且未患糖尿病的动物以及通过注射葡萄糖(在四氧嘧啶之前)或烟酰胺(在链脲佐菌素之前)预防糖尿病的动物中,EGF与肝受体的结合保持正常。我们得出结论,EGF受体表达降低是由糖尿病引起的,而非致糖尿病化合物对肝脏的毒性作用所致。

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