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马吲哚和46 - 034(山德士公司)对大鼠分离脂肪细胞葡萄糖氧化及胰岛素结合的影响。

The effects of mazindol and 46-034 (Sandoz) on glucose oxidation and insulin binding by rat isolated fat cells.

作者信息

Harrison L C, King-Roach A P

出版信息

Clin Exp Pharmacol Physiol. 1976 Sep-Oct;3(5):503-6. doi: 10.1111/j.1440-1681.1976.tb00630.x.

Abstract
  1. The anorexic agent mazindol and its major metabolite 46-034 (Sandoz) in high concentrations ( greater than 0-4 mM) abolished basal and insulin-stimulated conversion of 1-14C-glucose to 14CO2 by rat isolated fat cells. 2. High concentrations (1mM) also inhibited specific binding of 125 I-insulin to fat cells. 3. The observed effects appeared to be due in part to perturbation of the plasma membrane since there was a rise in the lactate dehydrogenase content of the incubation medium, increased 125I-insulin degradation and a reduction in cellular tritiated water space. 4. These effects are unlikely to be relevant to the therapeutic action of mazindol.
摘要
  1. 厌食药马吲哚及其主要代谢产物46 - 034(山德士公司)在高浓度(大于0.4 mM)时,可消除大鼠分离脂肪细胞将1 - 14C - 葡萄糖转化为14CO2的基础转化以及胰岛素刺激的转化。2. 高浓度(1 mM)也抑制125I - 胰岛素与脂肪细胞的特异性结合。3. 观察到的这些效应似乎部分归因于质膜的扰动,因为孵育培养基中乳酸脱氢酶含量增加、125I - 胰岛素降解增加以及细胞氚化水空间减少。4. 这些效应不太可能与马吲哚的治疗作用相关。

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