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首页> 外文期刊>Chemico-biological interactions >Anti-fibrotic cardio protective efficacy of aminoguanidine against streptozotocin induced cardiac fibrosis and high glucose induced collagen up regulation in cardiac fibroblasts
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Anti-fibrotic cardio protective efficacy of aminoguanidine against streptozotocin induced cardiac fibrosis and high glucose induced collagen up regulation in cardiac fibroblasts

机译:氨基胍对链脲佐菌素诱导的心脏纤维化和高糖诱导的心肌成纤维细胞胶原上调的抗纤维化心脏保护作用

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This study mainly focuses on cardio protective anti-fibrotic activity of aminoguanidine against streptozotocin induced cardiac fibrosis and high glucose induced collagen accumulation in cardiac fibroblasts. Dysregulation of matrix metalloproteinase especially 2 and 9 were considered to be responsible for the abnormal collagen deposition, which resulting improper cardiac contractile function in diabetic mice. Mice received a single dose of streptozotocin (100 mg/kg) through tail vein to induce diabetes. Normal and diabetic mice received aminoguanidine orally (100 mg/kg/day) throughout the study period of 8 weeks. Cardiac fibroblasts cultured and exposed to high glucose, aminoguanidine and both for 48 h. Collagen quantitatively estimated in both in vivo and in vitro models. Altered structural changes were studied using the Masson tri-chrome staining, TEM images of cardiac sections. Increased collagen and metalloproteinase activities were confirmed using gelatin zymography, western blotting and gene expression studies. The exact mechanism responsible for high glucose induced collagen up regulation in diabetic heart was incompletely understood. From this above in vivo and in vitro results, we conclude that, the cardio protective anti fibrotic activity of amino guanidine was mainly attributed by exhibiting the inhibitory efficacy against streptozotocin and high glucose induced collagen accumulation probably by inhibiting high glucose altered metalloproteinase-2 and -9 activities.
机译:这项研究主要侧重于氨基胍对链脲佐菌素诱导的心脏纤维化和高糖诱导的心肌成纤维细胞胶原积累的心脏保护性抗纤维化活性。基质金属蛋白酶特别是2和9的失调被认为是造成胶原蛋白沉积异常的原因,胶原蛋白沉积异常导致糖尿病小鼠心脏收缩功能异常。小鼠通过尾静脉接受单剂量的链脲佐菌素(100 mg / kg)诱导糖尿病。在整个8周的研究期内,正常和糖尿病小鼠口服氨基胍(100 mg / kg /天)。培养心脏成纤维细胞,并使其暴露于高葡萄糖,氨基胍和两者中48小时。在体内和体外模型中定量估计胶原蛋白。使用Masson三色染色,心脏切片的TEM图像研究了改变的结构变化。使用明胶酶谱,蛋白质印迹和基因表达研究证实了胶原蛋白和金属蛋白酶活性的增加。导致糖尿病患者高糖诱导胶原上调的确切机制尚不完全清楚。根据上述体内和体外结果,我们得出结论,氨基胍的心脏保护性抗纤维化活性主要归因于其对链脲佐菌素和高葡萄糖诱导的胶原蛋白积累的抑制作用,可能是通过抑制高葡萄糖改变的金属蛋白酶2和- 9项活动。

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