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作 者:刘贝贝[1] 阳琰[1] 李琪[1] 王贺 王莲地 LIU Beibei;YANG Yan;LI Qi;et al(Department of Endocrinology, Affiliated Hospital of Zunyi Medical College, Zunyi 563099, Chin)
出 处:《中国糖尿病杂志》2018年第1期55-58,共4页Chinese Journal of Diabetes
基 金:国家自然科学基金(81460148);贵州省科学技术基金[黔科合J字LK8(201319号)];遵义医学院博士启动基金[(2012)F-574]
摘 要:目的探讨1,25二羟基维生素D_3[1,25(OH)_2D_3]对T2DM大鼠肝脏的保护作用及机制。方法 100只雄性Wistar大鼠随机分成单纯T2DM组、1,25(OH)_2D_3干预组[1,25(OH)_2D_3+DM]、过氧化物酶体增殖物激活受体α(PPAR-α)抑制组[1,25(OH)_2D_3+PPAR-α抑制剂+DM]和正常对照(NC)组,每组各25只。6周后,测定各组FPG及血脂。ELISA检测肝脏组织中TG含量,RT-PCR检测大鼠肝脏组织中维生素D(VitD)受体(VDR)、PPAR-α、脂联素受体2(AdipoR2)mRNA表达水平。结果 1,25(OH)_2D_3+DM组肝脏中VDR、PPAR-α、AdipoR2 mRNA表达较T2DM组增加(t=20.32,5.92,9.10,P<0.05),TG含量较T2DM组减少(t=13.84,P<0.05)。结论 1,25(OH)_2D_3可能通过上调VDR基因的表达,进而上调AdipoR2、PPAR-α基因表达,从而减少肝脏TG的含量。Objective To explore the protective effect and mechanism of 1,25dihydroxyvitamin D_3[1,25(OH)2D3]on the liver of rats with type 2 diabetes(T2DM).Methods 100 male Wistar rats were randomly divided into four groups:T2DM group,Vitamin D(VitD)intervention group(VitD+DM group),peroxisome proliferator-activated receptors-alpha(PPAR-α)inhibitor group(VitD+DM+PPAR-αinhibitor group)and normal control group(NC group),with 25in each group.After 6 weeks later,fasting serum glucose(FPG)and blood lipid were measured.The content of triglyceride(TG)in liver tissue was detected by enzyme method.The expressions of Vitamin D receptor(VDR),PPAR-αand adiponectin receptor 2(AdipoR2)mRNA in rat liver was detected by real-time fluorescence quantitative reverse transcription-polymerase chain reaction(RT-PCR).Results The expressions of VDR,PPAR-αand Adipo R2 mRNA were significantly increased in VitD intervention group compared with T2DM group(t=20.32,5.92,9.10;P〈0.05).The content of TG in VitD+T2DM group was significantly lower than that in T2DM group(t=13.84,P〈0.05).Conclusion 1,25(OH)2D3 may up-regulate the expression of VDR gene and then up-regulate the expressions of AdipoR2 and PPAR-αthat decrease the content of TG in the liver.
关 键 词:1 25二羟基维生素D3 肝脏 脂联素受体2 维生素D受体 过氧化物酶体增殖物激活受体-Α
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