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胰岛素在人脂肪细胞中的受体结合及生物学效应

Receptor binding and biological effect of insulin in human adipocytes.

作者信息

Andersen O, Gliemann J, Gammeltoft S

出版信息

Diabetologia. 1977 Dec;13(6):589-93. doi: 10.1007/BF01236312.

Abstract

The binding of 125I-labelled insulin to human adipocytes was studied at 37 degrees C. The precipitability of the 125I-labelled insulin preparation (0.03 nmol/l) in trichloroacetic acid and the concentration of biologically active insulin (7.5 nmol/l) remained constant in buffer incubated with human adipocytes (100 microliter cells/ml suspension) for 30--60 minutes at 37 degrees C, whereas more than half of the insulin was inactivated by rat fat cells under the same conditions. A constant level of binding of 125I-labelled insulin (0.03 nmol/l) to human adipocytes was obtained after 45 minutes. The apparent dissociation constant of receptor binding was about 0.2 nmol/l as compared to about 2 nmol/l for rat adipocytes. Conversion of [UP14C]glucose to lipids was stimulated half-maximally by about 0.05 nmol/l of insulin (similar to rat adipocytes). Thus, half-maximal stimulation of human adipocytes was obtained with a recptor occupancy of about 20--30 per cent.

摘要

在37℃下研究了125I标记的胰岛素与人脂肪细胞的结合。125I标记的胰岛素制剂(0.03 nmol/l)在三氯乙酸中的沉淀性以及生物活性胰岛素的浓度(7.5 nmol/l),在37℃下与人类脂肪细胞(100微升细胞/毫升悬浮液)一起孵育30 - 60分钟的缓冲液中保持恒定,而在相同条件下,超过一半的胰岛素被大鼠脂肪细胞灭活。45分钟后,获得了125I标记的胰岛素(0.03 nmol/l)与人脂肪细胞的恒定结合水平。受体结合的表观解离常数约为0.2 nmol/l,而大鼠脂肪细胞约为2 nmol/l。[U-14C]葡萄糖向脂质的转化在约0.05 nmol/l胰岛素作用下达到最大刺激的一半(与大鼠脂肪细胞相似)。因此,人类脂肪细胞在受体占有率约为20 - 30%时获得最大刺激的一半。

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