瘦素对大鼠肝脏载脂蛋白M、载脂蛋白AI、载脂蛋白B和低密度脂蛋白受体表达的影响  被引量:5

Effects of leptin on the expressions of apolipoprotein M, apolipoprotein AI, lipoprotein B and low density fipoprotein receptor on rat liver

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作  者:狄冬梅[1] 张晓膺[1] 罗光华[2] 郑璐[1] 蒋波[1] Peter Nilsson-Ehle 徐宁[3] 

机构地区:[1]苏州大学附属第三医院心胸外科,常州213003 [2]苏州大学附属第三医院综合实验室,常州213003 [3]瑞典隆德大学医院实验医学研究所临床化学系

出  处:《中华实验外科杂志》2012年第10期1957-1959,共3页Chinese Journal of Experimental Surgery

基  金:国家自然科学基金资助项目(30972955、81071414)

摘  要:目的观察瘦素对正常SD大鼠肝脏载脂蛋白M(ApoM)、载脂蛋白AI(ApoAI)、载脂蛋白B(ApoB)和低密度脂蛋白受体(LDL—R)表达的影响。方法通过给健康SD大鼠尾静脉置管,微量注射泵持续泵入瘦素的方法建立高瘦素模型,对照组泵人生理盐水。6h后检测大鼠肝脏ApoM表达的变化,以及血清ApoM、脂蛋白的变化。通过建立离体肝灌注模型,检测肝脏ApoM mRNA的变化。结果在尾静脉实验中,瘦素组较生理盐水组血糖增加了14.68%(P〈0.01),胰岛素水平下降了68.82%(P〈0.05),大鼠肝脏ApoM、ApoB和LDL—RmRNA水平分别下降了55.15%(P〈0.05)、48.60%(P〈0.01)及40.43%(P〈0.05),而ApoAI表达增加了149.00%(P〈0.01)。但在离体肝灌注模型中,瘦素对ApoM、ApoAI、ApoB和LDL—R的表达无明显影响(P〉0.05)。结论瘦素对大鼠肝脏脂蛋白和LDL—R表达的影响可能通过其他信使介导,具体机制还需进一步研究。Objective To observe the effects of leptin on the expression of apolipoprotein M' s (ApoM) expression in HepG2 cells. Methods A series experiments were performed in the isolated rat' s liver perfusion and in normal rats. ApoM protein concentrations in serum were determined by the dot-blotting method and ApoM mRNA levels in liver tissues were determined by real-time reverse transcription-polymerase chain reaction (RT-PCR). Results After short time leptin administration, serum insulin levels were significantly decreased by 68. 82% (P 〈 0. 05 ), at the meanwhile blood glucose levels were increased by 14. 68 % (P 〈 0. 01 ) in the leptin treated rats compared to the control rats. Moreover, leptin could significantly decrease hepatic mRNA levels of ApoM,ApoB and LDL-R by 55.15% (P 〈0. 05) ,48.60% (P 〈0. 01 ) and 40.43% ( P 〈 0. 05 ), respectively, whereas ApoAI mRNA level was increased by 149.00% (P 〈0. 01 ) in the leptin treated rats. However, Leptin could not alter expression of ApoM, ApoAI, ApoB and LDL-R in the isolated liver perfusion ( P 〉 0. 05 ). Conclusion Leptin influences hepatic expressions of apolipoproteins and LDL-R needs secondary mediator in rats' body. The detailed mechanism needs further investigation.

关 键 词:载脂蛋白M 瘦素 载脂蛋白B 低密度脂蛋白受体 

分 类 号:R96[医药卫生—药理学]

 

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