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作 者:阳琰[1] 高琳[1] 邓华聪[2] 晏永慧[1] 李显文[1] 王小英[1] 廖鑫[1] 张晗[1]
机构地区:[1]遵义医学院附院内分泌科,563099 [2]重庆医科大学附一院内分泌科
出 处:《中华内分泌代谢杂志》2013年第8期696-699,共4页Chinese Journal of Endocrinology and Metabolism
基 金:贵州省优秀科技教育人才省长专项资金项目,贵州省科技合作项目
摘 要:目的观察脂联素对糖尿病大鼠模型肝脏中PPARα、胆固醇调节元件结合蛋白1C(SREBP-1C)、载脂蛋白A5(apoA5)表达及甘油三酯含量的影响。方法取60只雄性Wistar大鼠分成单纯糖尿病组(DM,n=20)、脂联素治疗组(Ad—APN+DM,n=20)和对照组(CON,n=20)。每组大鼠各取10只,采用实时荧光定量逆转录-聚合酶链反应(RT—PCR)、Western印迹分别对大鼠的肝脏组织中PPARα、SREBP-1C及apoA5基因、蛋白表达水平进行检测,并检测肝脏组织中甘油三酯含量。结果(1)DM组肝脏中PPARα、apoA5基因及蛋白表达比对照组显著降低(P〈0.05),SREBP-1C基因、蛋白表达及甘油三酯含量比对照组显著增加(P〈0.05);(2)脂联素干预组肝脏中PPARα、apoA5基因及蛋白表达较DM组增加(P〈0.05),而SREBP-1C表达下降(P〈0.05),甘油三酯含量明显降低(P〈0.05);(3)脂联素干预组肝脏中PPARα、SREBP-1C、apoA5基因及蛋白表达较对照组差异无统计学意义(P〉0.05),甘油三酯含量比较也无显著性差异(P〉0.05)。结论脂联素可能通过上调肝脏中PPARα、apoA5表达,抑制SREBP-1C的表达,从而降低甘油三酯水平。Objective To observe the gene and protein expression of PPARα, sterol regulatory element binding proteins-lC (SREBP-1C), and apolipoprotein (apo) A5 under adiponectiu intervention, as well as triglyeeride level in liver in diabetic rats. Methods Sixty male Wistar rats were assigned into 3 groups in random : diabetic group( DM, n = 20 ), adiponectin treated group ( Ad-APN + DM, n = 20 ), and control group ( CON, n = 20 ). 10 rats from each group were taken to detect the gene and protein expression of PPARc~, SREBP-1 C, and apoA5 in liver by real time-fluorescent quantitation reverse transcription-polymerase chain reaction and Western blot. The level of triglyceride in liver was determined. Results ( 1 ) The gene and protein expressions of PPARα, apoA5 were decreased in DM group( vs CON, P〈0.05 ). The expression of SREBP-1C and the level of triglyceride were increased (P〈0.05). (2)The expression of PPARoc and apoA5 in Ad-APN +DM group were increased while the expression of SREBP-1C was decreased ( all P〈0.05 ). ( 3 ) No difference was found in the expressions of PPARα, SREBP-1 C, and apoA5, as well as the levels of triglyceride between Ad-APN + DM group and CON group ( P 〉 0.05 ). Conclusions Adiponectin may upregulate PPARoL and apoA5 expressions but inhibit SREBP-1C expression in liver of diabetic rats, leading to decreased triglyceride content in liver of rats.
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