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非酒精性脂肪性肝病发生中Perilipin和ADRP表达变化实验研究

Analysis of Perilipin and ADRP changes in the nonalcoholic fatty liver disease
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摘要 目的:探讨高脂饮食诱导大鼠非酒精性脂肪性肝病(NAFLD)形成过程中,肝组织Perilipin(脂滴包被蛋白)和ADRP(脂肪分化相关蛋白)的表达变化及意义。方法:建立大鼠高脂饮食NAFLD模型并设正常对照组,观察时间点为建模后4w、8w和12w,观察大鼠肝组织病理变化,检测血浆游离脂肪酸及甘油三酯水平,免疫组织化学染色法检测肝组织中Perilipin和ADRP蛋白水平。结果:成功制作大鼠NAFLD实验模型,与正常组相比,NAFLD组大鼠血浆FFA水平和TG水平从第4w起显著升高(P<0.01),NAFLD组大鼠肝组织Perilipin蛋白表达水平显著低于正常组(P<0.01),ADRP蛋白表达水平显著高于同期正常组(P<0.01)。Perilipin及ADRP表达与FFA及TG具有显著相关性。结论:高脂饮食可制作NAFLD大鼠模型,Perilipin和ADRP与NAFLD的形成有关。 Objective:To investigate the changes of Perilipin and ADRP in the development of nonalcoholic fatty liver disease. Methods: Rat model of nonalcoholic fatty liver disease was established with fatty rich diet. The expression of Perilipin and ADRP in the rat's liver was dynamically detected by immunohistochemistry stainning at the 4th, 8th and 12th week. Meanwhile, FFA and TG levels in serum were detected. Results:Compared with the normal group, the serum levels of FFA and TG in NAFLD group increased significantly from beginning of the 4th week(P〈0. 01). The expression of Perilipin decreased significantly from the 4th week to 12th week, but the expression of ADRP increased significantly from beginning of the 4th week(P〈0. 01). The changes of Perilipin and ADRP were correlated with FFA and TG. Conclusion: High fat diet can be used to induce successfully NAFLD in rats. Perilipin and ADRP are involved in the formation of NAFLD.
作者 朱颖 陈东风
出处 《西南国防医药》 CAS 2008年第2期169-171,F0004,共4页 Medical Journal of National Defending Forces in Southwest China
基金 国家自然科学基金(2005CB522602)
关键词 非酒精性脂肪性肝病 游离脂肪酸 甘油三酯 脂滴包被蛋白 脂肪分化相关蛋白 nonalcoholic fatty liver disease FFA TG Perilipin ADRP
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  • 1ZELBER S S, NITZAN K D, HALPERN Z, et al. NAFLD and hyperinsulinemia are major determinants of serum ferritin levels[J]. J Hepatol, 2007, 46(4):700- 7007.
  • 2IMAI Y, VARELA G M,JACKSON M B, et al. Reduction of hepatosteatosis and lipid levels by an adipose differentiation-related protein antisense oligonucleotide[J]. Gastroenterology, 2007, 132(5):1947 - 1954.
  • 3HICKENBOTTOM S J, KIMMEL A R, LONDOS C, et al. Structure of a lipid droplet protein: the PAT family membcr TIP47[J]. Structure, 2004, 12(7):1199- 1207.
  • 4KOTOH K, NAKAMUTA M, FUKUSHIMA M, et al. Fertile femaks with nonalcoholic fatty liver discase (NAF1J)) have higher levels of ALT than postmenopausal females:implications for the influence of fertility on NAFLD[J]. Hepatogastroenterology, 2007, 54(73):224- 228.
  • 5MADAN K,BHARDWAJ P,THAREJA S,et al. Oxidant stress and antioxidant status among patients with nonalcoholic fatty liver disease (NAFLD)[J]. J Clin Gastroenterol, 2006, 40(10) : 930 - 935.
  • 6CHANG B H, CHAN L. Regulation of triglyeeride metabolism Ⅲ emerging role of lipid droplet protein ADFP in health and disease[J]. Am J Physiol Gastrointest Liver Physiol, 2007, 292 (6) :G1465 - 1468.
  • 7ACKERMAN W E, ROBINSON J M, KNISS D A.Association of PAT proteins with lipid storage droplets in term fetal membranes[J]. Placenta, 2007, 28(5 - 6) : 465 - 476.
  • 8KOVSAN J, BEN R R, SOUZA S C, et al. Regulation of adipocyte lipolysis by degradation of the perilipin protein: nelfinavir enhances lysosome - mediated perilipin proteolysis[J]. J Biol Chem, 2007, 282(30):21704 - 21711.
  • 9YAMAGUCHI T, OMATSU N,OMUKAE A, et al. Analysis of interaction partners for perilipin and ADRP on lipid droplets [J]. Mol Cell Biochem, 2006, 284(1 - 2): 167 - 173.

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