Draznin B, Sussman K E, Kao M, Sherman N
Medical Research Service, Veterans Administration Medical Center, Denver, Colorado 80220.
Endocrinology. 1988 Jun;122(6):2578-83. doi: 10.1210/endo-122-6-2578.
We have examined the relationship between insulin-stimulated 2-deoxyglucose uptake and cytosolic free calcium concentrations, [( Ca2+]i), in adipocytes isolated from 2- and 12-month-old rats. The basal rates of glucose uptake and the levels of cytosolic Ca2+ were only minimally reduced in 12-month-old animals. In contrast, insulin-stimulated glucose up-take and [Ca2+]i were significantly decreased in older adipocytes at all insulin concentrations (P less than 0.01). When the rate of glucose uptake was plotted as a function of [Ca2+]i, insulin-stimulated glucose uptake was almost identical in older and younger animals at any given level of [Ca2+]i. Similar to insulin, glyburide and K+ increased [Ca2+]i in both younger and older adipocytes. However, glyburide- and K+-elicited responses were lower in older rats (P less than 0.01). The effects of insulin, glyburide, and K+ on [Ca2+]i are mediated via voltage-dependent Ca2+ channels. Thus, the present observations suggest an impairment in either function and/or availability of the voltage-dependent Ca2+ channels in older animals. This was supported by the finding of reduced [3H]nitrendipine binding in adipocytes isolated from older animals (6.5% vs. 3.3% in 2- and 12-month-old rats, respectively; P less than 0.01). The results of these experiments indicate that the postreceptor changes in adipocyte responsiveness to insulin in aging may involve inadequate increases in [Ca2+]i. The latter probably occurs as a result of decreased availability and/or function of the voltage-dependent calcium channels.
我们研究了胰岛素刺激的2-脱氧葡萄糖摄取与从2月龄和12月龄大鼠分离的脂肪细胞中胞质游离钙浓度([Ca2+]i)之间的关系。12月龄动物的基础葡萄糖摄取率和胞质Ca2+水平仅略有降低。相比之下,在所有胰岛素浓度下,老年脂肪细胞中胰岛素刺激的葡萄糖摄取和[Ca2+]i均显著降低(P<0.01)。当将葡萄糖摄取率绘制为[Ca2+]i的函数时,在任何给定的[Ca2+]i水平下,老年和年轻动物中胰岛素刺激的葡萄糖摄取几乎相同。与胰岛素类似,格列本脲和K+可增加年轻和老年脂肪细胞中的[Ca2+]i。然而,老年大鼠中格列本脲和K+引起的反应较低(P<0.01)。胰岛素、格列本脲和K+对[Ca2+]i的作用是通过电压依赖性Ca2+通道介导的。因此,目前的观察结果表明老年动物中电压依赖性Ca2+通道的功能和/或可用性受损。从老年动物分离的脂肪细胞中[3H]尼群地平结合减少的发现支持了这一点(2月龄和12月龄大鼠分别为6.5%和3.3%;P<0.01)。这些实验结果表明,衰老过程中脂肪细胞对胰岛素反应性的受体后变化可能涉及[Ca2+]i增加不足。后者可能是由于电压依赖性钙通道的可用性和/或功能降低所致。