Defalque D, Brandt N, Ketelslegers J M, Thissen J P
Unité de Diabétologie et Nutrition, School of Medicine, The University of Louvain, B-1200 Brussels, Belgium.
Am J Physiol. 1999 Mar;276(3):E565-72. doi: 10.1152/ajpendo.1999.276.3.E565.
Sepsis induces a state of growth hormone (GH) resistance associated with a decrease of circulating insulin-like growth factor (IGF) I, a GH-dependent anabolic hormone mainly produced by the liver. To address the mechanisms that might trigger GH insensitivity in sepsis, we investigated the regulation of liver GH receptor (GHR) and its gene expression by endotoxin. Endotoxin injection in rats decreased serum IGF-I and liver GH-binding sites after 10 h. In contrast to liver GHR, circulating GH-binding protein (GHBP) levels were not significantly reduced after endotoxin injection. The parallel decrease in IGF-I and GHR and in their corresponding liver mRNAs suggests that decreased serum IGF-I and liver GHR were likely to result from decreased liver synthesis. Although GH administration in control animals significantly enhanced serum IGF-I, it did fail to prevent the decline in serum IGF-I and liver GH-binding sites in endotoxemic rats. In this study, we showed that endotoxin injection induces a state of GH insensitivity associated with decreased liver GHR. This decline in GHR, which cannot be prevented by exogenous GH, might contribute to the GH insensitivity observed in sepsis.
脓毒症会引发一种生长激素(GH)抵抗状态,这与循环胰岛素样生长因子(IGF)-I水平降低有关,IGF-I是一种主要由肝脏产生的依赖GH的合成代谢激素。为了探究脓毒症中可能引发GH不敏感的机制,我们研究了内毒素对肝脏GH受体(GHR)及其基因表达的调控。给大鼠注射内毒素10小时后,血清IGF-I和肝脏GH结合位点减少。与肝脏GHR不同,注射内毒素后循环GH结合蛋白(GHBP)水平没有显著降低。IGF-I和GHR及其相应肝脏mRNA的平行下降表明,血清IGF-I和肝脏GHR降低可能是肝脏合成减少所致。尽管给对照动物注射GH可显著提高血清IGF-I水平,但它未能阻止内毒素血症大鼠血清IGF-I和肝脏GH结合位点的下降。在本研究中,我们表明注射内毒素会引发一种与肝脏GHR降低相关的GH不敏感状态。这种GHR的下降不能被外源性GH所阻止,可能是脓毒症中观察到的GH不敏感的原因之一。