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High sucrose/fat diet and isosorbide mononitrate increase insulin resistance, nitric oxide production and myocardial apoptosis in a hypertensive rat model

机译:高蔗糖/脂肪饮食和异山梨醇单硝酸盐升高胰岛素抵抗,一氧化氮生产和高血压大鼠模型中的心肌细胞凋亡

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The present study aimed to investigate the association between insulin resistance (IR), nitric oxide (NO) production and myocardial apoptosis in a background of coexisting hypertension in a rodent animal model. A hypertensive rat model was established by feeding Wistar and spontaneously hypertensive rats (SHR) with a high sucrose/fat (HSF) diet for 12 weeks, in conjunction with isosorbide mononitrate (ISMN). Increased IR, NO content, apoptotic gene and protein expression, and morphological alterations within rat myocardium were evaluated. Following a total of 12 weeks of feeding with HSF and ISMN resulted in increased IR and NO content within the myocardial tissue of Wistar and SHR rats. HSF and ISMN activated myocardial apoptosis by downregulating the gene transcription and protein expression levels of the anti-apoptotic B-cell lymphoma 2 (Bcl-2), and increasing the pro-apoptotic Bcl-2 associated X protein. Apoptosis was demonstrated by DNA fragmentation in terminal deoxynucleotidyl-transferase-mediated dUTP nick end labelling assay. In all experiments, the combination of HSF and ISMN was associated with more pronounced effects, indicating the possible synergistic effects. In addition, the correlation analysis in the Wistar rats fed with HSF only, revealed a positive association between NO production and IR. The results of the present study indicated that HSF and ISMN simultaneously increased IR, NO production and myocardial apoptosis in the hypertensive rat model, and may therefore contribute to investigations into the long-term clinical use of ISMN in hypertensive patients.
机译:本研究旨在探讨啮齿动物模型共存高血压背景下胰岛素抵抗(IR),一氧化氮(NO)产生和心肌凋亡的关联。通过喂养Wistar和自发性高血压大鼠(SHR)与高蔗糖/脂肪(HSF)饮食的高血压大鼠(HSF)饮食成立高血压大鼠模型,同时与异山梨醇单硝酸盐(ISMN)结合。评估IR增加的IR,无含量,凋亡基因和蛋白质表达,以及大鼠心肌内的形态改变。随着HSF的总共喂养12周,导致Wistar和ShR大鼠心肌组织内的IRM产生增加,没有含量。通过下调抗凋亡B细胞淋巴瘤2(Bcl-2)的基因转录和蛋白表达水平,并增加促凋亡Bcl-2相关X蛋白,通过下调基因转录和蛋白质表达水平来激活心肌凋亡。通过末端脱氧核苷酸转移酶介导的DUTP切口末端标记测定的DNA碎片证明了细胞凋亡。在所有实验中,HSF和ISMN的组合与更明显的效果相关,表明可能的协同效应。此外,仅喂养HSF的Wistar大鼠的相关性分析,揭示了无生产和IR之间的正相关。本研究的结果表明,HSF和ISMN同时增加了IR,无缓解大鼠模型中的生产和心肌细胞凋亡,因此可能有助于调查ISMN在高血压患者中的长期临床应用。

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