Castro M, Pedrosa D, Osuna J I
Departamento de Bioquímica y Biología Molecular, Facultad de Medicina, Universidad de Granada, Spain.
Experientia. 1993 Oct 15;49(10):850-3. doi: 10.1007/BF01952596.
We investigated the effect of aging on glucose uptake, glucose-induced O2 consumption, glucose-induced 45Ca movements, and calmodulin content to elucidate age-related impairment of glucose-induced insulin release in pancreatic islets of Wistar rats. Intact pancreatic islets from old (24-month-old) rats showed impaired glucose-induced insulin release; glucose uptake and O2 consumption were lower in old than in young (2-month-old) or adult (12-month-old) rats. Moreover, 45Ca uptake and calmodulin content were decreased in pancreatic islets from older rats, which explained the impairment in glucose-induced insulin release in aging. No major differences between the 3 age groups in glucose-induced 45Ca efflux in pancreatic islets were observed.
我们研究了衰老对葡萄糖摄取、葡萄糖诱导的氧气消耗、葡萄糖诱导的45Ca转运以及钙调蛋白含量的影响,以阐明Wistar大鼠胰岛中与年龄相关的葡萄糖诱导的胰岛素释放受损情况。来自老年(24月龄)大鼠的完整胰岛显示葡萄糖诱导的胰岛素释放受损;老年大鼠的葡萄糖摄取和氧气消耗低于年轻(2月龄)或成年(12月龄)大鼠。此外,老年大鼠胰岛中的45Ca摄取和钙调蛋白含量降低,这解释了衰老过程中葡萄糖诱导的胰岛素释放受损的原因。在3个年龄组的胰岛中,未观察到葡萄糖诱导的45Ca外流有重大差异。