血管紧张素Ⅱ受体拮抗剂减低大鼠体内脂肪

被引：7

作者：

窦京涛 ^{[1
]}

Steve Zorad ^{[2
]}

Juan M Saavedra ^{[3
]}

机构：

[1] 解放军总医院内分泌科

[2] 斯洛伐克科学院实验内分泌研究所

[3] 美国国立卫生研究院

来源：

军医进修学院学报 | 2006年 / 01期

关键词：

受体,血管紧张素; 脂肪类; 大鼠;

D O I：

暂无

中图分类号：

R96 [药理学];

学科分类号：

100602 ; 100706 ;

摘要：

目的:探讨血管紧张素Ⅱ受体拮抗剂-Candesratan对大鼠脂肪细胞形态和功能的影响。方法:20只雄性W istarKyoto大鼠分为治疗组和对照组,分别予以口服Candesartan(10 mg.kg-1.d-1)和安慰剂,每周监测摄食量和体重变化。17周后处死大鼠,收集附睾和肾周围脂肪组织并称重;同时分离附睾脂肪细胞,测量细胞直径,抽提并测定脂肪组织甘油三酯;测定血浆生化、胰岛素、瘦素和脂联素;通过RT-PCR测定附睾脂肪瘦素、脂联素和前脂肪细胞因子-1mRNA基因表达。结果:Candesartan治疗组大鼠体重和体内脂肪含量较对照组明显减低,附睾脂肪细胞缩小,细胞构成升高,但总细胞数无明显表化;两组间血糖和胰岛素无显著差异,治疗组血瘦素水平和脂肪组织瘦素mRNA表达均降低,而血脂联素水平升高、脂肪组织脂联素mRNA表达增加,前脂肪细胞因子-1mRNA表达则无变化。结论:血管紧张素Ⅱ受体拮抗剂使脂肪细胞缩小,从而减少脂肪组织含量,同时增加脂联素的合成和分泌。

引用

页码：4 / 6

页数：3

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