首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Insulin requirement for contraction of cultured rat glomerular mesangial cells in response to angiotensin II: possible role for insulin in modulating glomerular hemodynamics.
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Insulin requirement for contraction of cultured rat glomerular mesangial cells in response to angiotensin II: possible role for insulin in modulating glomerular hemodynamics.

机译:胰岛素对培养的大鼠肾小球系膜细胞响应血管紧张素II收缩的胰岛素需求:胰岛素在调节肾小球血流动力学中的可能作用。

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摘要

One proposed role of glomerular mesangial cells is the regulation of glomerular blood flow by contraction. Alterations in the contractile activity of mesangial cells could lead to alterations in glomerular hemodynamics and then to glomerular injury. In this study, the effects of glucose and insulin on the contractile response of cloned homogeneous cultures of rat glomerular mesangial cells to angiotensin II were examined. Cells were cultured in normal-glucose medium (D-glucose at 200 mg/dl) and normal-glucose medium with added insulin (4 microgram/ml). To mimic the diabetic state, cells were cultured in high-glucose medium (D-glucose at 550 mg/dl) and high-glucose medium with added insulin. The media contained 20% fetal calf serum. Cells were grown for at least 1 wk in medium prior to contraction experiments. All clones of mesangial cells grown in the presence of additional insulin, in either normal- or high-glucose media, underwent contraction when treated with angiotensin II (0.001-10 microM). Seventy-five percent of the cells contracted. Not one contracted cell was seen in cultures grown without insulin in the medium, even when exposed to 10 microM angiotensin II. From these data, it appears that insulin may be required for the contractile response of mesangial cells to angiotensin II. Loss of contractile activity by mesangial cells in low- or no-insulin conditions (e.g., juvenile diabetes mellitus) could lead to a marked increase in glomerular blood flow, ultimately resulting in glomerulosclerosis.
机译:肾小球系膜细胞的一种建议作用是通过收缩调节肾小球的血流。肾小球系膜细胞收缩活性的改变可能导致肾小球血流动力学改变,进而导致肾小球损伤。在这项研究中,研究了葡萄糖和胰岛素对大鼠肾小球系膜细胞克隆同质培养物对血管紧张素II收缩反应的影响。在正常葡萄糖培养基(D-葡萄糖为200 mg / dl)和添加了胰岛素的正常葡萄糖培养基(4微克/毫升)中培养细胞。为了模拟糖尿病状态,将细胞在高葡萄糖培养基(D-葡萄糖为550 mg / dl)和高葡萄糖培养基中添加胰岛素进行培养。培养基含有20%的胎牛血清。在收缩实验之前,将细胞在培养基中生长至少1周。当使用血管紧张素II(0.001-10 microM)处理时,在正常或高葡萄糖培养基中在其他胰岛素存在下生长的所有系膜细胞克隆均发生收缩。百分之七十五的细胞收缩。即使暴露于10 microM血管紧张素II,在培养基中不添加胰岛素的培养物中也看不到一个收缩细胞。从这些数据看来,胰岛素可能是肾小球系膜细胞对血管紧张素II的收缩反应所必需的。肾小球系膜细胞在低胰岛素或无胰岛素条件下(例如青少年糖尿病)的收缩活性丧失可能导致肾小球血流量显着增加,最终导致肾小球硬化。

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