Kaino Y, Hirai H, Ito T, Kida K
Department of Pediatrics, Ehime University School of Medicine, Japan.
Diabetes Res Clin Pract. 1996 Sep;34(1):7-11. doi: 10.1016/s0168-8227(96)01326-5.
It has been shown that prophylactic exogenous insulin treatment prevents the development of insulin-dependent diabetes mellitus (IDDM) in animal models and humans. In this study, we examined whether the development of diabetes and insulitis in female non-obese diabetic (NOD) mice could be affected by prophylactic administration of insulin-like growth factor I (IGF-I), which shares structural homology with insulin and has insulin-like metabolic effects. Two experiments which differed in duration and dosage of IGF-I treatment were carried out. In the first experiment, animals were treated from 4 to 9 weeks of age with IGF-I (17.9 nmol/day at 4-5 weeks of age and 35.9 nmol/day at 6-9 weeks of age) and observed up to 34 weeks of age. In the second experiment, the animals were treated from 4 to 34 weeks of age with IGF-I (1.79 nmol/day at 4-5 weeks of age, 3.59 nmol/day at 6-9 weeks of age, and 5.38 nmol/day at 10-34 weeks of age). The former treatment could significantly delay the onset of diabetes (P < 0.05) and decrease the insulitis score at 10 weeks of age (P < 0.01). On the other hand, the latter treatment did not affect the incidence of diabetes, the age at onset or the insulitis score. Our results suggest that the IGF-I treatment at the early age may provide protection against autoimmune beta-cell destruction in NOD mice.
研究表明,预防性外源性胰岛素治疗可预防动物模型和人类胰岛素依赖型糖尿病(IDDM)的发生。在本研究中,我们检测了预防性给予胰岛素样生长因子I(IGF-I)是否会影响雌性非肥胖糖尿病(NOD)小鼠糖尿病和胰岛炎的发生,IGF-I与胰岛素具有结构同源性,并具有胰岛素样代谢作用。进行了两项IGF-I治疗持续时间和剂量不同的实验。在第一个实验中,动物在4至9周龄时接受IGF-I治疗(4至5周龄时为17.9 nmol/天,6至9周龄时为35.9 nmol/天),并观察至34周龄。在第二个实验中,动物在4至34周龄时接受IGF-I治疗(4至5周龄时为1.79 nmol/天,6至9周龄时为3.59 nmol/天,10至34周龄时为5.38 nmol/天)。前一种治疗可显著延迟糖尿病的发病(P<0.05),并降低10周龄时的胰岛炎评分(P<0.01)。另一方面,后一种治疗对糖尿病发病率、发病年龄或胰岛炎评分没有影响。我们的结果表明,早期给予IGF-I治疗可能为NOD小鼠的自身免疫性β细胞破坏提供保护。