Couturier E
Diabetes Res Clin Pract. 1985;1(6):343-7. doi: 10.1016/s0168-8227(86)80047-x.
Twelve type II diabetics were treated with gliclazide, a potent hypoglycaemic sulfonylurea, for 5 months. Plasma immunoreactive insulin (IRI), connecting peptide (C-peptide) and immunoreactive glucagon (IRG) were measured during a 2 h oral glucose tolerance test (OGTT) before and during gliclazide therapy. The OGTT improved in 7 patients. In those patients IRI concentrations were significantly more elevated during than before the treatment period. By contrast, gliclazide treatment did not affect the hepatic extraction of insulin (estimated by the molar ratio of C-peptide to IRI) nor the inappropriate glucagon release commonly observed in this type of patients.
12名II型糖尿病患者接受了格列齐特(一种强效降糖磺脲类药物)治疗,为期5个月。在格列齐特治疗前及治疗期间,于2小时口服葡萄糖耐量试验(OGTT)过程中测定血浆免疫反应性胰岛素(IRI)、连接肽(C肽)和免疫反应性胰高血糖素(IRG)。7名患者的OGTT有所改善。在这些患者中,治疗期间IRI浓度较治疗前显著升高。相比之下,格列齐特治疗既不影响胰岛素的肝脏摄取(通过C肽与IRI的摩尔比估算),也不影响这类患者中常见的不适当胰高血糖素释放。