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Impact of interleukin-6 on the glucose metabolic capacity in rat liver

机译:白细胞介素6对大鼠肝脏葡萄糖代谢能力的影响

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The actute phase reaction mediated by the proinflammatory cytokine IL6 initiates a number of metabolic changes in the liver, which may contribute to the pathogenesis of the septic shock during prolonged exposition. Here, the impact of IL6 on the hepatic glucose providing capacity was studied by monitoring glycogen degradation and the expression of the gluconeogenic phosphoenolpyruvate carboxykinase (PCK1) in rat livers during the daily feeding rhythm. Eight hours after i.p. injection of IL6, mRNA levels of α2-macroglobulin, a prominent acute phase reactant in rat liver, were elevated as shown by Northern blot analysis and in situ hybridization (ISH). PCK1 mRNA levels were decreased by IL6 to 50% of levels in untreated animals due to the reduction of PCK1 mRNA in the periportal zone of the liver as shown by ISH. PCK1 enzyme activity was not affected by IL6. Glycogen degradation was accelerated by IL6, which led to nearly complete depletion of glycogen pools in periportal areas 8 h after IL6 injection. This was very likely due to inhibition of glycogen pool replenishment. Thus, the depletion of glycogen stores in the liver might contribute to the impairment of hepatic glucose production during prolonged acute phase challenge.
机译:由促炎细胞因子IL6介导的致动相反应在肝脏中引发许多代谢变化,这可能导致长期暴露期间败血性休克的发病机理。在这里,通过监测日常进食节律期间大鼠肝中糖原降解和糖异生性磷酸烯醇丙酮酸羧化激酶(PCK1)的表达,研究了IL6对肝葡萄糖提供能力的影响。 i.p.后八小时如Northern印迹分析和原位杂交(ISH)所示,注射IL6后,大鼠肝脏中显着的急性期反应物α2-巨球蛋白的mRNA水平升高。如ISH所示,由于未处理动物中PCK1 mRNA的水平降低了IL6,降至未治疗动物水平的50%,这是由于肝脏肝周区PCK1 mRNA的减少所致。 PCK1酶活性不受IL6的影响。 IL6加速了糖原的降解,导致IL6注射后8 h周围区域糖原池几乎完全耗尽。这很可能是由于糖原池补充的抑制。因此,在长期急性期攻击过程中,肝中糖原存储的消耗可能会导致肝葡萄糖生成的损害。

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