Cayón A, Crespo Javier, Mayorga M, Guerra A, Pons-Romero F
Gastroenterology and Hepatology Unit, University Hospital Marqués de Valdecilla, School of Medicine, Santander, Spain.
Liver Int. 2006 Nov;26(9):1065-71. doi: 10.1111/j.1478-3231.2006.01337.x.
The main aim of this study was to examine the relationship of the leptin system in steatosis and nonalcoholic steatohepatitis (NASH). The study also analysed the pathogenic role of the leptin system in the development of hepatic fibrosis and its relation with the TGF-beta1 system.
The study included 90 subjects, 55 with NASH and 35 with simple steatosis. Gene expression of leptin, leptin receptor and TGF-beta mRNA was analysed by real-time PCR on liver tissue. Leptin serum levels were determined by RIA. Leptin receptor expression was also assessed by immunohistochemistry.
Increased expression was found for leptin receptor mRNA (P=0.0016) and its protein (P<0.05) in patients with NASH, especially those with fibrosis. There was a marked increase in gene expression of TGF-beta1 in patients with NASH (P=0.0002). A strong correlation was demonstrated between leptin receptor gene expression and TGF-beta1 gene expression (P=0.023). No leptin expression was found in the liver tissue. All patients showed a marked hyperleptinemia, which was closely related to the anthropometric characteristics analysed and independent of development or not of NASH.
The results of the study demonstrate for the first time increased leptin receptor expression in liver tissue and its relationship with overexpression of TGF-beta1 and the degree of hepatic fibrosis.
本研究的主要目的是探讨瘦素系统在脂肪变性和非酒精性脂肪性肝炎(NASH)中的关系。该研究还分析了瘦素系统在肝纤维化发展中的致病作用及其与转化生长因子-β1(TGF-β1)系统的关系。
该研究纳入90名受试者,其中55名患有NASH,35名患有单纯性脂肪变性。通过对肝组织进行实时聚合酶链反应(PCR)分析瘦素、瘦素受体和TGF-β mRNA的基因表达。通过放射免疫分析(RIA)测定血清瘦素水平。还通过免疫组织化学评估瘦素受体表达。
在NASH患者中,尤其是那些患有纤维化的患者,发现瘦素受体mRNA(P = 0.0016)及其蛋白(P < 0.05)表达增加。NASH患者中TGF-β1的基因表达显著增加(P = 0.0002)。瘦素受体基因表达与TGF-β1基因表达之间存在强相关性(P = 0.023)。在肝组织中未发现瘦素表达。所有患者均表现出明显的高瘦素血症,这与所分析的人体测量学特征密切相关,且与NASH的发生与否无关。
该研究结果首次证明肝组织中瘦素受体表达增加及其与TGF-β1过表达和肝纤维化程度的关系。