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Effect of KIOM-79 on Diabetes-Induced Myocardial Fibrosis in Zucker Diabetic Fatty Rats

机译:KIOM-79对Zucker糖尿病脂肪大鼠糖尿病诱导心肌纤维化的影响

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摘要

KIOM-79, a herbal mixture of parched Puerariae radix, gingered Magnoliae cortex, Glycyrrhizae radix, and Euphorbiae radix, has a strong inhibitory effect on advanced glycation end products (AGEs) formation. We investigated the beneficial effects of KIOM-79 on cardiac fibrosis in Zucker diabetic fatty (ZDF) rats. KIOM-79 (50 or 500 mg/kg/day) was orally administered for 13 weeks. AGEs formation and collagen expression in the myocardium were assessed by immunohistochemistry. The expression levels of the receptor for AGEs (RAGE), transforming growth factor-β1 (TGF-β1), collagen IV, fibronectin, urotensin II, and urotensin II receptor were examined in the myocardial tissue of ZDF rats. KIOM-79 treatment at 500 mg/kg inhibited the accumulation of AGEs, reduced RAGE mRNA and protein expression, and reduced the upregulation of cardiac fibrogenic factors, such as fibronectin and collagen IV, in heart of ZDF rats. Additionally, KIOM-79 ameliorated urotensin II/receptor gene expression in the cardiac tissue of ZDF rats. Our findings indicate that KIOM-79 diminishes cardiac fibrosis in ZDF rats by preventing AGEs accumulation and RAGE overexpression and by modulating the cardiac urotensin II/receptor pathway, which decreases the amount of profibrotic factors, such as TGF-β1, fibronectin, and collagen in cardiac tissue.
机译:KIOM-79,炎热葛根,gingered皮质厚朴,甘草,和基数锦的草药混合物,对晚期糖基化终产物(AGEs)的形成较强的抑制作用。我们研究了在Zucker糖尿病肥胖(ZDF)大鼠心肌纤维化KIOM-79的有益效果。 KIOM-79(50或500毫克/公斤/天)口服给药13周。的AGEs的形成和胶原表达在心肌中,通过免疫组织化学评估。受体的年龄(RAGE)的表达水平,转化生长因子β1(TGF-β1),胶原蛋白IV,纤连蛋白,尾加压素II和尾加压素II受体在ZDF大鼠的心肌组织进行了研究。 KIOM-79治疗在500毫克/公斤抑制的AGEs积聚,减少RAGE mRNA和蛋白的表达,并减少了心脏纤维化因素,如纤连蛋白和胶原蛋白IV的上调,在ZDF大鼠的心脏。此外,KIOM-79在ZDF大鼠的心脏组织改善尾加压素II /受体基因的表达。我们的研究结果表明,KIOM-79通过防止的AGE积累和RAGE过表达和通过调节心脏尾加压素II /受体途径,从而减少促纤维化因子如TGF-β1,纤连蛋白,和胶原蛋白的量减少心脏纤维化ZDF大鼠心脏组织。

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