Neonatal stimulation of beta-cells reduces the incidence and delays the onset of diabetes in a barrier-protected breeding colony of BB rats.

A K Hansen, K Josefsen, C Pedersen, K Buschard
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引用次数: 5

Abstract

The off-spring in a barrier maintained colony of spontaneously type 1 diabetic BB/Wor/Mol-BB rats was treated with a daily injection of either saline, forskolin, arginine, glucose or both glucose and arginine for the first six days after birth. The incidence was reduced from 88% to 72% by the neonatal stimulation with arginine and glucose in combination, which also delayed the onset time from 76.0 +/- 2.2 days to 88.1 +/- 2.3 days. No such effect was observed after stimulation with either one of the compounds. Neonatal stimulation with forskolin also delayed the onset to 87.9 +/- 3.8 days, however without reducing the incidence. A higher incidence of diabetes was observed in the barrier-protected rats taking part in this study than in an earlier study using BB rats of the same origin, but kept under conventional conditions.

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在屏障保护的BB大鼠繁殖群体中,新生儿刺激β细胞可降低糖尿病的发病率并延缓其发病。
在屏障维持的自发性1型糖尿病BB/Wor/Mol-BB大鼠的后代中,在出生后的前6天,每天注射生理盐水、福斯可林、精氨酸、葡萄糖或葡萄糖和精氨酸同时注射。精氨酸和葡萄糖联合刺激可使新生儿发病时间从76.0 +/- 2.2天延迟至88.1 +/- 2.3天,发生率从88%降至72%。用任何一种化合物刺激后都没有观察到这种效果。用福斯克林刺激新生儿也将发病延迟至87.9±3.8天,但没有降低发病率。与先前使用相同来源的BB大鼠在常规条件下进行的研究相比,在参与本研究的屏障保护大鼠中观察到更高的糖尿病发病率。
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