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糖肝康对糖尿病脂肪肝模型大鼠肝脏AdipoR_2 mRNA表达的影响 被引量:3

Effect of Tanggankang on mRNA Expression of AdipoR_2 in the Liver of Diabetic-fatty Liver Rat Model
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摘要 目的:研究糖肝康对糖尿病脂肪肝模型大鼠肝脏组织中AdipoR_2 mRNA表达的影响。方法:高糖+高脂+小剂量链脲佐菌素腹腔注射建立糖尿病脂肪肝大鼠模型,并设对照组进行观察。药物干预12周后,采用RT-PCR方法检测糖肝康对肝脏组织中AdipoR_2mRNA表达的影响。结果:模型大鼠的肝脏组织中AdipoR_2 mRNA表达水平较低(0.143±0.046),糖肝康可上调其在肝脏组织中的mRNA表达(小剂量组为0.202±0.052,大剂量组为0.212±0.049),与模型对照组比较,差异有统计学意义(P<0.05),且大剂量组表达高于降糖甲对照组(0.176±0.065)。结论:糖尿病脂肪肝的糖脂代谢紊乱可能与AdipoR_2的低水平表达相关,糖肝康可通过上调AdipoR_2 mRNA表达水平,在糖、脂代谢等方面到积极作用,值得进一步深入研究。 Objective:To observe the effect of Tanggankang on mRNA expression of AdipoR,in the liver of diabetic-fatty liver rat model.Method:The rat model was made with STZ and high-fat and high-glucose diet.After 12 weeks of drug intervention,the rats were killed and the livers were removed,and the mRNA expression of AdipoR,in the livers was observed by the method of RT-PCR. Result:The mRNA expression of AdipoR2 in the livers was significantly increased,and Tanggankang could lower the expression of AdipoR_2 in the livers in a dose-dependent manner.Conclusion:The abnormal expression of AdipoR,can be one of the mechanisms of diabetic -fatty liver.Tanggankang has a promising protective effect on the liver through adjusting the expression of AdipoR2,which deserves further research.
出处 《中国药师》 CAS 2012年第11期1533-1535,共3页 China Pharmacist
基金 山东省中医药科学技术研究项目(编号:2011-038) 山东省科学技术厅科学技术发展计划项目(编号:003130130)
关键词 糖肝康 糖尿病脂肪肝 RT-PCR 脂联素受体2 Tanggankang Diabetic-fatty liver RT-PCR AdipoR_2
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  • 1张晓静,宋鲁成.糖尿病肝损害的中西医认识[J].内蒙古中医药,2009(2):95-96. 被引量:4
  • 2齐君,李俊利,常福厚.中药降血脂作用的研究进展[J].内蒙古中医药,2007,26(1):59-60. 被引量:15
  • 3赵新军,张敏州.通冠胶囊对高脂大鼠血脂水平和血浆炎症因子的影响[J].中西医结合心脑血管病杂志,2007,5(10):951-952. 被引量:6
  • 4Guan Y,Br~-,yer M D.Targeting peroxis~mle proliferalor-aclivated rec~ptors(PPARs)in kidney and urologic' disease.Minerva Urol Nefi'ol,2002.54(2):65-79.
  • 5Moo/ha V K.Lirdgrenl C M.E,'ikscon K F.el al.PGC-lalpha- responsive genes involved ill oxidalive phosphorlation are coordinately downregulated in human diabetes.Nat Gene|.2003. 34(3):267-273.
  • 6Yoon J C,Puigserver P,Chen G,et aI.Control ot" hepalic glueoneogenesis through the transcripliomll eoaeliwltor PGC-I. Nalure,2001,413(6852): 131 - 138.
  • 7Koo S H.Satoh H.Herzig S.e/aI.PGC-I pro, moles insulin resislant.e in liver through PPAR-alpha-dependenl indt,c/ion of TRB-3.NaI Med,2004,10(5):530-534.
  • 8Hmlmnm~tedl A,Jansson P A.Wesslau C.e! al.Reduced exln~ssion of PGC-1 and Insulin-signaling molecules in adipose tissue is associated with insulin resislance.Bioehem Biophys Res Co,nmun, 2003,301 (2):578-582.
  • 9Tordjmml K,Bemal-Mizrachi C,Zemmly L,et "aI.PPAR ot deficiency reduces insulin resistance and athemselerosis In at~~E-mJll mice. J Clin I nvest,2001,107(8): 1025-1034.
  • 10严启新,杨健武.中医药治疗高脂血症研究进展[J].云南中医中药杂志,1998,19(2):38-39. 被引量:4

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