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脂联素/AdipoR2 的下调与肥胖小鼠的脂肪性肝炎有关。

Downregulation of adiponectin/AdipoR2 is associated with steatohepatitis in obese mice.

机构信息

Department of Surgery, University of South Florida, Tampa, FL, USA.

出版信息

J Gastrointest Surg. 2009 Nov;13(11):2043-9. doi: 10.1007/s11605-009-1032-2. Epub 2009 Sep 18.

Abstract

BACKGROUND

Recent evidence suggests that obesity is associated with hypo-adiponectinmia and chronic inflammation. Adiponectin regulates fat storage, energy expenditure, and inflammation. We propose that high fat diet induces steatohepatitis, reduces serum adiponectin, and liver adiponectin receptors.

METHODS

A 4-week-old C57BL male mice were fed high fat diet (n = 8) or regular chow (control; n = 6) for 7 weeks. Body weight, liver weight, and serum adiponectin were measured. Liver sections were stained with hematoxylin and eosin and oil red for fat content. Liver homogenates were used for protein (immunoblotting) and mRNA (reverse transcription PCR) of Toll-like receptor 4 (TLR4), tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-6, sterol regulatory element-binding proteins (SREBP)-1c, and adiponectin receptors (AdipoR1/AdipoR2) in addition to nuclear phorsphorylated p65NF-kappaB. Gels were quantified using densitometry; t test was used, and p < 0.05 was significant.

RESULTS

High fat diet increased body (50%) and liver weight (33%), as well as hepatocyte fat content and ballooning. Mice fed high fat diet exhibited reduced serum adiponectin and liver AdipoR2. High fat diet increased hepatic levels of SREBP-1c, TLR4, TNF-alpha, and IL-6 protein and mRNA and increased activation of p65NF-kappaB.

CONCLUSIONS

Diet-induced liver steatosis is associated with increased lipogensis, upregulation of pro-inflammatory cytokines, and transcription factors as well as downregulation of AdipoR2. Reduction in serum adiponectin suggests that adiponectin signaling may be the crosslink between high fat diet, hepatic inflammation, and nonalcoholic fatty liver disease.

摘要

背景

最近的证据表明,肥胖与低 adiponectinmia 和慢性炎症有关。 adiponectin 调节脂肪储存、能量消耗和炎症。我们假设高脂肪饮食会诱导 steatohepatitis,降低血清 adiponectin 和肝脏 adiponectin 受体。

方法

4 周龄 C57BL 雄性小鼠用高脂肪饮食(n = 8)或常规饲料(对照;n = 6)喂养 7 周。测量体重、肝重和血清 adiponectin。肝组织切片用苏木精和伊红及油红染色检测脂肪含量。肝匀浆用于 Toll 样受体 4(TLR4)、肿瘤坏死因子 alpha(TNF-alpha)、白细胞介素(IL)-6、固醇调节元件结合蛋白(SREBP)-1c 和 adiponectin 受体(AdipoR1/AdipoR2)的蛋白(免疫印迹)和 mRNA(反转录 PCR),以及核磷酸化 p65NF-kappaB。使用密度计对凝胶进行定量;使用 t 检验,p < 0.05 为差异有统计学意义。

结果

高脂肪饮食增加了体重(50%)和肝重(33%),以及肝细胞脂肪含量和气球样变。高脂肪饮食组小鼠血清 adiponectin 和肝脏 AdipoR2 减少。高脂肪饮食增加了肝脏 SREBP-1c、TLR4、TNF-alpha 和 IL-6 蛋白和 mRNA 的水平,并增加了 p65NF-kappaB 的激活。

结论

饮食诱导的肝脂肪变性与脂肪生成增加、促炎细胞因子和转录因子上调以及 AdipoR2 下调有关。血清 adiponectin 减少表明 adiponectin 信号可能是高脂肪饮食、肝炎症和非酒精性脂肪性肝病之间的交叉点。

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