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首页> 外文期刊>Chemico-biological interactions >Betanin reduces the accumulation and cross-links of collagen in high-fructose-fed rat heart through inhibiting non-enzymatic glycation
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Betanin reduces the accumulation and cross-links of collagen in high-fructose-fed rat heart through inhibiting non-enzymatic glycation

机译:甜菜碱通过抑制非酶糖基化来减少高果糖喂养的大鼠心脏中胶原蛋白的积累和交联

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We attempted to determine whether betanin (from natural pigments) that has antioxidant properties would be protective against fructose-induced diabetic cardiac fibrosis in Sprague-Dawley rats. Fructose water solution (30%) was accessed freely, and betanin (25 and 100 mg/kg/d) was administered by intragastric gavage continuously for 60 d. Rats were sacrificed after overnight fast. The rat blood and left ventricle were collected. In vitro antiglycation assay in bovine serum albumin/fructose system was also performed. In rats treated only with fructose, levels of plasma markers: glucose, insulin, HOMA and glycated hemoglobin rised, left ventricle collagen accumulated and cross-linked, profibrotic factor-transforming growth factor (TGF)-beta 1 and connective tissue growth factor (CTGF) protein expression increased, and soluble collagen decreased, compared with those in normal rats, showing fructose induces diabetic cardiac fibrosis. Treatment with betanin antagonized the changes of these parameters, demonstrating the antifibrotic role of betanin in the selected diabetic models. In further mechanistic study, betanin decreased protein glycation indicated by the decreased levels of protein glycation reactive intermediate (methylglyoxal), advanced glycation end product (N-epsilon-(carboxymethyl) lysine) and receptors for advanced glycation end products (AGEs), antagonized oxidative stress and nuclear factor-kappa B activation elicited by fructose feeding, suggesting inhibition of glycation, oxidative stress and nuclear factor-kappa B activation may be involved in the antifibrotic mechanisms. Betanin also showed anitglycative effect in BSA/fructose system, which supported that anitglycation was involved in betanin's protective roles in vivo. Taken together, the potential for using betanin as an auxiliary therapy for diabetic cardiomyopathy deserves to be explored further. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
机译:我们试图确定具有抗氧化特性的甜菜碱(来自天然色素)是否对果糖诱导的Sprague-Dawley大鼠糖尿病性心肌纤维化具有保护作用。自由获取果糖水溶液(30%),并通过胃内灌胃连续60 d施用甜菜碱(25和100 mg / kg / d)。禁食过夜后处死大鼠。收集大鼠血液和左心室。还进行了牛血清白蛋白/果糖系统的体外抗糖化试验。在仅用果糖治疗的大鼠中,血浆标志物的水平升高:葡萄糖,胰岛素,HOMA和糖化血红蛋白升高,左心室胶原蛋白积累并交联,促纤维化因子转化生长因子(TGF)-β1和结缔组织生长因子(CTGF)与正常大鼠相比,蛋白表达增加,可溶性胶原蛋白减少,表明果糖可诱导糖尿病性心肌纤维化。用甜菜碱处理可拮抗这些参数的变化,从而证明了甜菜碱在所选糖尿病模型中的抗纤维化作用。在进一步的机理研究中,甜菜碱降低了蛋白质糖基化作用,这是由蛋白质糖基化反应性中间体(甲基乙二醛),高级糖基化终产物(N-ε-(羧甲基)赖氨酸)和高级糖基化终产物(AGEs)的受体水平降低所指示的。果糖喂养引起的应激和核因子-κB活化,表明糖基化抑制,氧化应激和核因子-κB活化可能参与抗纤维化机制。甜菜碱在BSA /果糖系统中也显示出抗糖化作用,这证明了抗糖化作用与甜菜碱在体内的保护作用有关。综上所述,将甜菜碱用作糖尿病性心肌病辅助治疗的潜力值得进一步探讨。 (C)2014 Elsevier Ireland Ltd.保留所有权利。

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