Tanira M O, Furman B L
Department of Pharmacology, College of Medicine, Sultan Qaboos University, Muscat-123, Oman.
Pharmacol Res. 1999 May;39(5):349-56. doi: 10.1006/phrs.1998.0446.
Many reports suggest that extrapancreatic actions contribute to the antidiabetic effect of sulphonylurea drugs (SUs). In this work, the ability of two SUs, namely, gliclazide and glibenclamide, to augment insulin action was studied in vivo. Both drugs elevated the plasma concentration of immunoreactive insulin (IRI) and lowered the plasma concentrations of glucose and non-esterified fatty acids (NEFA) in normal intact rats. These changes were not reproduced in alloxan-diabetic or eviscerated rats. The actions of insulin on plasma glucose and NEFA were not augmented by gliclazide in alloxan-diabetic rats. Neither gliclazide nor glibenclamide (given acutely and for 30 days) augmented the actions of exogenously administered insulin in reducing plasma glucose or NEFA concentrations in intact or eviscerated animals. It was concluded that these SUs do not produce their acute or chronic effects on blood glucose by augmenting the actions of insulin.
许多报告表明,磺脲类药物(SUs)的降糖作用与其胰腺外作用有关。在本研究中,我们在体内研究了两种磺脲类药物(格列齐特和格列本脲)增强胰岛素作用的能力。在正常完整大鼠中,这两种药物均能提高免疫反应性胰岛素(IRI)的血浆浓度,并降低血浆葡萄糖和非酯化脂肪酸(NEFA)的浓度。在四氧嘧啶糖尿病大鼠或去内脏大鼠中,这些变化并未重现。在四氧嘧啶糖尿病大鼠中,格列齐特并未增强胰岛素对血浆葡萄糖和NEFA的作用。无论是格列齐特还是格列本脲(急性给药30天),均未增强外源性胰岛素在完整或去内脏动物中降低血浆葡萄糖或NEFA浓度的作用。由此得出结论,这些磺脲类药物并非通过增强胰岛素作用来产生其对血糖的急性或慢性影响。