首页> 美国卫生研究院文献>The Journal of Physiology >Leptin activates ATP-sensitive potassium channels in the rat insulin-secreting cell line CRI-G1.
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Leptin activates ATP-sensitive potassium channels in the rat insulin-secreting cell line CRI-G1.

机译:瘦素激活大鼠胰岛素分泌细胞系CRI-G1中的ATP敏感性钾通道。

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摘要

1. Whole-cell current-clamp recordings demonstrate that leptin (0.3-10 nm) hyperpolarizes CRI-G1 insulin-secreting cells. This effect is slow on onset and is not reversed on washout of the leptin. 2. Voltage-clamp recordings indicate that leptin activates a potassium conductance in the presence of intracellular ATP (5 mm), but has not effect in its absence. Following activation of ATP-sensitive K+ (KATP) current by diazoxide (0.2 mm), addition of leptin did not alter cell membrane potential or potassium current further. 3. The leptin-induced hyperpolarization and increased potassium conductance are completely inhibited by the application of the sulphonylureas tolbutamide (100 microM) and glibenclamide (0.5 microM). 4. Cell-attached and inside-out single-channel recordings indicate that leptin activates tolbutamide-sensitive KATP channels in CRI-G1 insulin-secreting cells.
机译:1.全细胞电流钳记录表明,瘦素(0.3-10 nm)使CRI-G1胰岛素分泌细胞超极化。该作用起效缓慢,并且在瘦素洗脱后不会逆转。 2.电压钳记录表明,瘦素在存在细胞内ATP(5毫米)的情况下激活钾电导,但在不存在时不起作用。用二氮嗪(0.2 mm)激活ATP敏感性K +(KATP)电流后,添加瘦素不会进一步改变细胞膜电位或钾电流。 3.磺脲类甲苯磺丁酰胺(100 microM)和格列本脲(0.5 microM)的应用完全抑制了瘦素诱导的超极化和钾电导的增加。 4.细胞附着和由内而外的单通道记录表明,瘦素激活CRI-G1胰岛素分泌细胞中对甲苯磺丁酰胺敏感的KATP通道。

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