首页> 外文OA文献 >Retinol binding Protein-4 circulating levels were higher in nonalcoholic fatty liver disease vs. histologically normal liver from morbidly obese women.
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Retinol binding Protein-4 circulating levels were higher in nonalcoholic fatty liver disease vs. histologically normal liver from morbidly obese women.

机译:在非酒精性脂肪肝疾病中,视黄醇结合蛋白4循环水平高于病态肥胖妇女的组织学正常肝脏。

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摘要

We aimed to analyze the retinol binding protein-4 (RBP4) messenger RNA (mRNA) expression profiles in adipose tissues and liver of morbidly obese (MO) women with or without nonalcoholic fatty liver disease (NAFLD), and to study the relationships with other pro- and anti-inflammatory adipokines in vivo and in vitro. We performed a cross-sectional analysis of subcutaneous adipose tissue (SAT), visceral adipose tissue (VAT) and liver samples from four lean and 45 MO women with or without NAFLD by enzyme-linked immunosorbent assay and real-time reverse transcription-PCR. We also studied RBP4 expression in HepG2 hepatocytes under various inflammatory stimuli. Circulating RBP4 levels were higher in MO women, and specifically, in MO subjects with NAFLD compared with normal liver controls (lean and MO). RBP4 liver expression was higher in nonalcoholic steatohepatitis (NASH)-moderate/severe than in NASHmild. Overall RBP4 gene expression was higher in liver than in adipose tissues. Among them, the higher expression corresponded to SAT. VAT expression was lower in the MO cohort. In HepG2, RBP4 mRNA expression was reduced by tumor necrosis factor (TNF)-α and increased by adiponectin treatment. In conclusion, the results obtained in MO women with NAFLD, brings up the use of RBP4 and other adipokines as a panel of noninvasive molecular biomarkers when NAFLD is suspected. Further studies are needed with other obesity groups.
机译:我们旨在分析视黄醇结合蛋白4(RBP4)信使RNA(mRNA)在患有或不患有非酒精性脂肪性肝病(NAFLD)的病态肥胖(MO)妇女的脂肪组织和肝脏中的表达特征,并研究其与其他人的关系体内和体外的促炎和抗炎脂肪因子。我们通过酶联免疫吸附测定和实时逆转录-PCR对来自有或没有NAFLD的四名瘦和45个MO妇女的皮下脂肪组织(SAT),内脏脂肪组织(VAT)和肝脏样本进行了横断面分析。我们还研究了在各种炎症刺激下HepG2肝细胞中RBP4的表达。与正常肝对照组(瘦肉和MO)相比,MO妇女(尤其是患有NAFLD的MO受试者)的循环RBP4水平更高。在非酒精性脂肪性肝炎(NASH)中/重度,RBP4肝表达高于NASHmild。肝脏中总体RBP4基因表达高于脂肪组织。其中,较高的表达对应于SAT。 MO队列中的VAT表达较低。在HepG2中,RBP4 mRNA表达被肿瘤坏死因子(TNF)-α降低,而脂联素处理则使RBP4 mRNA表达增加。总之,在怀疑患有NAFLD的MO女性NAFLD患者中获得的结果表明,使用RBP4和其他脂肪因子作为一组非侵入性分子生物标记物。其他肥胖人群需要进一步研究。

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