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实验性糖尿病酮症酸中毒中胰岛素与分离的脂肪细胞结合受损。

Impaired insulin binding to isolated adipocytes in experimental diabetic ketoacidosis.

作者信息

Whittaker J, Cuthbert C, Hammond V, Alberti K G

出版信息

Diabetologia. 1981 Dec;21(6):563-8. doi: 10.1007/BF00281550.

Abstract

Insulin sensitivity in vivo and insulin binding in vitro to adipocytes have been studied in streptozotocin diabetic rats with ketoacidosis. Insulin sensitivity in vivo measured as the acute (20 min) fall in blood glucose in response to an insulin infusion of 1 U/kg body weight per hour correlated positively with arterial blood pH (r = 0.92, p less than 0.01: n - 38). At pH less than 6.9 there was no fall in blood glucose. For studies in insulin binding to adipocytes ketoacidotic animals were divided into a group with moderate ketoacidosis (pH greater than 7.0) and a second group with severe ketoacidosis (pH less than 6.9). Insulin binding to adipocytes was maximal in cells from both ketoacidotic and from normal rats at pH 7.6-7.8. Total binding was decreased in he diabetic rats (P less than 0.01) and this was more marked in the severely diabetic group (p less than 0.001) at all pHs studied. At pH 7.4, 125I-insulin binding was decreased in diabetics compared with normal rats (0.89 +/- 0.14 versus 2.0 +/- 0.24% with 2 x 10(5) cells/ml: n = 6;p less than 0.01) and also in the severe compared with the moderate ketoacidotic rats (0.5 +/- 0.08%/2 X 10(5) cells; n = 6, p less than 0.05). Equilibrium binding studies showed that there was a small decrease in apparent affinity in adipocytes from both groups of diabetics (KD = 2.8 +/#- 0.2 X 10-9 mol/l, n = 6 in moderate ketoacidosis; 2.5 +/- 0.3 X 10-9 mol/l, n = 6 in severe ketoacidosis) compared with control animals (KD = 1.8 +/- 0.15 X 10-9 mol/l, n = 6). Scatchard analysis revealed that there was also a decrease in receptor concentration which was greater in the severely ketoacidotic group. These findings may explain in part the insulin resistance of severe ketoacidosis.

摘要

在患有酮症酸中毒的链脲佐菌素糖尿病大鼠中,对体内胰岛素敏感性和体外胰岛素与脂肪细胞的结合进行了研究。体内胰岛素敏感性通过每小时输注1 U/kg体重胰岛素后血糖在20分钟内的急性下降来衡量,其与动脉血pH呈正相关(r = 0.92,p < 0.01:n = 38)。当pH小于6.9时,血糖没有下降。为了研究胰岛素与脂肪细胞的结合,将酮症酸中毒动物分为中度酮症酸中毒组(pH > 7.0)和重度酮症酸中毒组(pH < 6.9)。在pH 7.6 - 7.8时,来自酮症酸中毒大鼠和正常大鼠的脂肪细胞中胰岛素结合达到最大值。在所有研究的pH值下,糖尿病大鼠的总结合量均降低(P < 0.01),在重度糖尿病组中更为明显(p < 0.001)。在pH 7.4时,与正常大鼠相比,糖尿病大鼠的125I胰岛素结合量降低(2×10⁵个细胞/ml时,分别为0.89±0.14%和2.0±0.24%:n = 6;p < 0.01);与中度酮症酸中毒大鼠相比,重度酮症酸中毒大鼠的结合量也降低(0.5±0.08%/2×10⁵个细胞;n = 6,p < 0.05)。平衡结合研究表明,两组糖尿病大鼠脂肪细胞的表观亲和力均略有下降(中度酮症酸中毒组KD = 2.8±0.2×10⁻⁹mol/l,n = 6;重度酮症酸中毒组KD = 2.5±0.3×10⁻⁹mol/l,n = 6),而对照动物的KD = 1.8±0.15×10⁻⁹mol/l,n = 6。Scatchard分析显示,受体浓度也降低,在重度酮症酸中毒组中降低更为明显。这些发现可能部分解释了重度酮症酸中毒的胰岛素抵抗。

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