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The Regulatory Influence of Galarmin on the Level and Activity of Rat Tissue Metalloproteins after Doxorubicin-induced Nephro- and Cardiotoxicity

机译:加拉明对阿霉素诱导的肾毒性和心脏毒性后大鼠组织金属蛋白水平和活性的调节作用

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摘要

Doxorubicin (DR) is a potential antineoplastic drag that is used for therapy of different types of malignant tumors (leukemia, lymphoma, mammary tumor, lung, ovarian, pancreatic tumor etc.). However, the long-term use of DR leads to irreversible cardiomyopathy and nephropathy due to DR-induced formation of free oxygen radicals that disturb the functionality of the mitochondria, membranes, and nuclei of cells. The mechanisms of DR-induced cardiotoxicity and nephrotoxicity associated with changes in the activity of antioxidant metalloproteins (Cu, Zn-SOD, Mn-SOD, and catalase) and prooxidant metalloproteins (acidic isoforms of cytochrome (cyt) b_(558) and cyt C) in heart and kidney cells are not clear. Here we tried to evaluate these biochemical factors.
机译:阿霉素(DR)是一种潜在的抗肿瘤药,可用于治疗不同类型的恶性肿瘤(白血病,淋巴瘤,乳腺肿瘤,肺,卵巢,胰腺肿瘤等)。但是,DR的长期使用会导致不可逆的心肌病和肾病,这是由于DR诱导的氧自由基的形成干扰了线粒体,细胞膜和细胞核的功能。 DR引起的心脏毒性和肾毒性的机制与抗氧化剂金属蛋白(Cu,Zn-SOD,Mn-SOD和过氧化氢酶)和前氧化剂金属蛋白(细胞色素(cyt)b_(558)和cyt C的酸性同工酶)活性变化相关)在心脏和肾脏中的细胞尚不清楚。在这里,我们试图评估这些生化因素。

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