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Effect of multiple cytokines plus bacterial endotoxin on glucose and nitric oxide production by cultured hepatocytes.

机译:多种细胞因子加细菌内毒素对培养的肝细胞产生葡萄糖和一氧化氮的影响。

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摘要

Treatment of cultured hepatocytes with a combination of cytokines, including tumour necrosis factor-alpha, interferon-gamma and interleukin-1 beta, plus lipopolysaccharide resulted in a time-dependent induction of nitric oxide (NO) synthase (as measured by NO2- (+) NO3- production) and inhibition of hepatic gluconeogenesis and glycogen breakdown. The inhibition of glucose release was comparable with the observed following treatment of rats with lipopolysaccharide or treatment of isolated hepatocytes with artificial NO donors. In addition, this effect was also evident with all substrates tested that enter the gluconeogenic pathway below the level of phosphoenolpyruvate carboxykinase, suggesting that this combination of cytokines may underlie the inhibition of gluconeogenesis observed in endotoxic shock. The maximal inhibition of glucose output required the presence of all the cytokines plus lipopolysaccharide, whereas the induction of NO synthase was independent of the lipopolysaccharide when the cytokines were employed. Inclusion of interferon-gamma was essential to obtain a maximal response for either parameter. Inclusion of 1 mM N(G)-monomethyl-L-arginine in the incubation abolished the increase in NO2- (+) NO3- observed with the complete cytokine mixture and various combinations; however, it failed to prevent the inhibition in glucose output, indicating that mechanisms other than NO underlie the cytokine-induced inhibition of glucose release.
机译:用细胞因子(包括肿瘤坏死因子-α,干扰素-γ和白介素-1β)以及脂多糖联合处理培养的肝细胞会导致时间依赖性的一氧化氮(NO)合酶诱导(以NO2-(+ )产生NO3-)并抑制肝糖异生和糖原分解。葡萄糖释放的抑制作用与用脂多糖处理大鼠或用人工NO供体处理分离的肝细胞后观察到的相当。此外,在所有测试的进入糖异生途径低于磷酸烯醇丙酮酸羧激酶水平的糖异生途径的底物上,这种作用也很明显,表明这种细胞因子的结合可能是内毒素休克中糖异生抑制的基础。葡萄糖输出的最大抑制需要所有细胞因子加脂多糖的存在,而当使用细胞因子时,NO合酶的诱导与脂多糖无关。包含干扰素-γ对于获得任一参数的最大响应至关重要。在培养中加入1 mM N(G)-单甲基-L-精氨酸消除了用完整的细胞因子混合物和各种组合观察到的NO2-(+)NO3-的增加;然而,它不能阻止对葡萄糖输出的抑制,表明除NO外的其他机制是细胞因子诱导的葡萄糖释放抑制的基础。

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