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首页> 外文期刊>Bioscience Reports >Deleterious Effects of Supplementation with Dehydroepiandrosterone Sulphate or Dexamethasone on Rat Insulin-Secreting Cells Under In Vitro Culture Condition
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Deleterious Effects of Supplementation with Dehydroepiandrosterone Sulphate or Dexamethasone on Rat Insulin-Secreting Cells Under In Vitro Culture Condition

机译:在体外培养条件下补充硫酸脱氢表雄酮或地塞米松对大鼠胰岛素分泌细胞的有害作用

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Dehydroepiandrosterone (DHEA) and glucocorticoids are steroid hormones synthesised in the adrenal cortex. Administration of DHEA, its sulphate derivative, DHEAS, and more controversially dexamethasone (DEX), a synthetic glucocorticoid, have beneficial effects in diabetic animals. Cultivating BRIN-BD11 cells for 3?days with either DHEAS (30?μM) or DEX (100?nM), reduced total cell number and reduced cell viability and cellular insulin content. DHEAS-treated cells had poor glucose responsiveness and regulated insulin release, coupled with reduced basal insulin release. In contrast, DEX-treated cells lacked responsiveness to glucose and membrane depolarisation, and both protein kinase A (PKA) and protein kinase C (PKC) secretory pathways were desensitised. Therefore, we conclude that this steroid hormone and synthetic glucocorticoid are not beneficial to pancreatic β-cells in vitro.
机译:脱氢表雄酮(DHEA)和糖皮质激素是在肾上腺皮质中合成的类固醇激素。 DHEA,其硫酸盐衍生物,DHEAS以及更具争议性的地塞米松(DEX)(一种合成的糖皮质激素)的给药对糖尿病动物具有有益的作用。用DHEAS(30?μM)或DEX(100?nM)培养BRIN-BD11细胞3天,减少了细胞总数,降低了细胞活力和细胞胰岛素含量。 DHEAS处理的细胞具有较差的葡萄糖反应性和调节的胰岛素释放,以及降低的基础胰岛素释放。相反,经DEX处理的细胞缺乏对葡萄糖和膜去极化的反应性,并且蛋白激酶A(PKA)和蛋白激酶C(PKC)分泌途径均被脱敏。因此,我们得出结论,这种类固醇激素和合成的糖皮质激素在体外对胰腺β细胞无益。

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