Masiello P, Broca C, Gross R, Roye M, Manteghetti M, Hillaire-Buys D, Novelli M, Ribes G
Istituto di Patologia Generale, University of Pisa, Italy.
Diabetes. 1998 Feb;47(2):224-9. doi: 10.2337/diab.47.2.224.
We took advantage of the partial protection exerted by suitable dosages of nicotinamide against the beta-cytotoxic effect of streptozotocin (STZ) to create a new experimental diabetic syndrome in adult rats that appears closer to NIDDM than other available animal models with regard to insulin responsiveness to glucose and sulfonylureas. Among the various dosages of nicotinamide tested in 3-month-old Wistar rats (100-350 mg/kg body wt), the dosage of 230 mg/kg, given intraperitoneally 15 min before STZ administration (65 mg/kg i.v.) yielded a maximum of animals with moderate and stable nonfasting hyperglycemia (155 +/- 3 vs. 121 +/- 3 mg/dl in controls; P < 0.05) and 40% preservation of pancreatic insulin stores. We also evaluated beta-cell function both in vitro and in vivo 4-9 weeks after inducing diabetes. In the isolated perfused pancreas, insulin response to glucose elevation (5-11 mmol/l) was clearly present, although significantly reduced with respect to controls (P < 0.01). Moreover, the insulin response to tolbutamide (0.19 mmol/l) was similar to that observed in normal pancreases. Perfused pancreases from diabetic animals also exhibited a striking hypersensitivity to arginine infusion (7 mmol/l). In rats administered STZ plus nicotinamide, intravenous glucose tolerance tests revealed clear abnormalities in glucose tolerance and insulin responsiveness, which were interestingly reversed by tolbutamide administration (40 mg/kg i.v.). In conclusion, this novel NIDDM syndrome with reduced pancreatic insulin stores, which is similar to human NIDDM in that it has a significant response to glucose (although abnormal in kinetics) and preserved sensitivity to tolbutamide, may provide a particularly advantageous tool for pharmacological investigations of new insulinotropic agents.
我们利用适当剂量的烟酰胺对链脲佐菌素(STZ)的β细胞毒性作用所产生的部分保护作用,在成年大鼠中创建了一种新的实验性糖尿病综合征。就胰岛素对葡萄糖和磺脲类药物的反应性而言,该综合征比其他现有动物模型更接近非胰岛素依赖型糖尿病(NIDDM)。在3个月大的Wistar大鼠(体重100 - 350 mg/kg)中测试的各种烟酰胺剂量中,在静脉注射STZ(65 mg/kg)前15分钟腹腔注射230 mg/kg的剂量,产生了最多数量的具有中度且稳定的非空腹高血糖的动物(对照组为121±3 mg/dl,实验组为155±3 mg/dl;P < 0.05),并且胰腺胰岛素储备保留了40%。我们还在诱导糖尿病后4 - 9周对β细胞功能进行了体外和体内评估。在离体灌注胰腺中,对葡萄糖升高(5 - 11 mmol/l)的胰岛素反应明显存在,尽管相对于对照组显著降低(P < 0.01)。此外,对甲苯磺丁脲(0.19 mmol/l)的胰岛素反应与正常胰腺中观察到的相似。糖尿病动物的灌注胰腺对精氨酸输注(7 mmol/l)也表现出显著的超敏反应。在给予STZ加烟酰胺的大鼠中,静脉葡萄糖耐量试验显示葡萄糖耐量和胰岛素反应性明显异常,有趣的是,给予甲苯磺丁脲(40 mg/kg静脉注射)后这些异常得到了逆转。总之,这种新型的NIDDM综合征胰腺胰岛素储备减少,与人类NIDDM相似,即对葡萄糖有显著反应(尽管动力学异常)且对甲苯磺丁脲保持敏感性,可能为新型促胰岛素分泌剂的药理学研究提供特别有利的工具。