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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Comparative effects of Aliskiren and Telmisartan in high fructose diet-induced metabolic syndrome in rats
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Comparative effects of Aliskiren and Telmisartan in high fructose diet-induced metabolic syndrome in rats

机译:阿利吉仑和替米沙坦在高果糖饮食诱导的代谢综合征中的比较作用

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Fructose is a commonly used sweetener associated with diets that increase the prevalence of metabolic syndrome (MS). Inhibition of the Fenin-angiotensin system (RAS) has been consistently demonstrated to reduce MS. However, there has been 110 direct comparison among different pharmacological modes of inhibiting the RAS concerning their effects on MS. This study investigated the effect of aliskiren, a direct renin inhibitor, versus telmisailan, an angiotensin If-receptor blocked, in the treatment of fructose-induced MS in rats. MS was induced by high fructose (FRC) diet feeding for 12 weeks. Oral administrations of telmisartan (TEL, 5 mg/kg), aliskiren (ALS, 30 mg/kg) or vehicle were started in the last 4 weeks. Results showed that administration of either TEL or ALS with FRC diet equally ameliorated the metabolic parameters (glucose level, oral glucose tolerance test, insulin resistance and serum lipids profile), systolic blood pressure and oxidative stress markers (malondialdehyde, nitric oxide, reduced ! glutathione levels and catalase activity). Additionally, the effects of TEL and ALS were associated with a decrease in body composition index and attenuation of liver index, serum liver enzyme activities and hepatic expressions of inflammatory and fibrotic markers (tumor necrosis factor-a, nuclear factor kappaB and transforming growth factor-beta) with a significant increase in hepatic glucose transporter-2 and peroxisome proliferator-activated receptors-alpha and gamma expressions. The results suggested that, at indicated dosage, ALS has ameliorative effect equal to that of TEL against FRC-induced metabolic and hepatic disorders; implying that drugs which inhibit the RAS, by different mode of inhibition, profoundly affect fructose-induced MS in rats. (C) 2015 Elsevier B.V. All rights reserved.
机译:果糖是与饮食相关的常用甜味剂,可增加代谢综合征(MS)的患病率。 Fenin-血管紧张素系统(RAS)的抑制作用一直被证明可以降低MS。但是,在抑制RAS的不同药理模式对MS的影响之间进行了110次直接比较。这项研究调查了直接肾素抑制剂阿利吉仑与血管紧张素If受体阻断剂替米塞兰在大鼠果糖诱导的MS中的治疗作用。高果糖(FRC)饮食喂养12周可诱发MS。在最近4周内开始口服替米沙坦(TEL,5 mg / kg),阿利吉仑(ALS,30 mg / kg)或赋形剂。结果表明,无论是TEL还是ALS与FRC饮食配合使用,均可以改善代谢参数(葡萄糖水平,口服葡萄糖耐量试验,胰岛素抵抗和血清脂质谱),收缩压和氧化应激指标(丙二醛,一氧化氮,还原性谷胱甘肽)水平和过氧化氢酶活性)。此外,TEL和ALS的作用还与人体成分指数降低和肝脏指数降低,血清肝酶活性以及炎性和纤维化标记物(肿瘤坏死因子-a,核因子kappaB和转化生长因子- β),并显着增加肝葡萄糖转运蛋白2和过氧化物酶体增殖物激活受体的α和γ表达。结果表明,在指定剂量下,ALS对FRC引起的代谢和肝病的缓解作用与TEL相当。暗示以不同的抑制方式抑制RAS的药物会深刻影响果糖诱导的大鼠MS。 (C)2015 Elsevier B.V.保留所有权利。

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