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Regulation of hepatic glucose metabolism by leptin in pig and rat primary hepatocyte cultures.

机译:瘦素在猪和大鼠原代肝细胞培养物中对肝葡萄糖代谢的调节。

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Direct effects of leptin on gluconeogenesis in rat hepatocytes are equivocal, and model systems from other species have not been extensively explored in assessing the regulation of glucose metabolism by leptin. Therefore, the goal of the present study was to compare the effects of leptin on gluconeogenesis in pig and rat hepatocyte cultures as well as to investigate an underlying mechanism of action at the level of phosphoenolpyruvate carboxykinase (PEPCK). In rat hepatocytes, leptin exposure (3 h, 50 and 100 nM) attenuated glucagon-stimulated hepatic gluconeogenesis by 35 and 38% (P < 0.05), respectively. However, leptin did not produce any significant acute effect in pig hepatocytes. Leptin exposure for 24 h failed to produce any significant effect on gluconeogenesis in either rat or pig hepatocytes cultured in the presence of glucagon or dexamethasone. Mechanistically, there was a 25-35% decrease (P < 0.05) in glucagon-induced PEPCK mRNA levels in rat but not pig hepatocytes cultured with leptin. This effect on PEPCK mRNA was not due to an alteration in the relative abundance of the leptin receptor or the ability of PEPCK to respond to cAMP. The nonuniformity of the effects of leptin on gluconeogenesis in pig and rat hepatocytes indicates differences in leptin action between species. Furthermore, the unique action of leptin in porcine hepatocytes points to the utility of this model system for biomedical research and also underscores the value of comparative studies.
机译:瘦素对大鼠肝细胞糖异生的直接作用是模棱两可的,在评估瘦素对葡萄糖代谢的调节方面,尚未广泛探索其他物种的模型系统。因此,本研究的目的是比较瘦素对猪和大鼠肝细胞培养中糖异生的影响,并研究在磷酸烯醇丙酮酸羧激酶(PEPCK)水平上潜在的作用机制。在大鼠肝细胞中,瘦素暴露(3 h,50和100 nM)分别使胰高血糖素刺激的肝糖异生减少35%和38%(P <0.05)。但是,瘦素在猪肝细胞中没有产生任何明显的急性作用。在存在胰高血糖素或地塞米松的情况下培养的大鼠或猪肝细胞中,瘦素暴露24 h未能对糖异生产生任何显着影响。从机制上讲,胰高血糖素诱导的大鼠PCPCK mRNA水平降低了25-35%(P <0.05),但瘦素培养的猪肝细胞没有下降。对PEPCK mRNA的这种作用不是由于瘦素受体相对丰度的改变或PEPCK对cAMP的反应能力所致。瘦素对猪和大鼠肝细胞糖异生作用的影响不均匀,表明物种之间瘦素作用的差异。此外,瘦素在猪肝细胞中的独特作用表明该模型系统可用于生物医学研究,也强调了比较研究的价值。

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