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Effect of catecholestrogen administration during adriamycin-induced cardiomyopathy in ovariectomized rat.

机译:去甲肾上腺皮质激素对阿霉素诱发的心肌病的影响。

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The therapeutical beneficial effect of estrogen-derived metabolites or catecholestrogens is controversial. These molecules are produced during estrogen therapy based on 17-beta-estradiol treatment. The metabolization of 17-beta-estradiol is carried out in brain, kidney or liver, and triggers different products such as 2- and 4- hydroxyestradiol (2OH and 4OH). These products have shown antioxidant properties against oxidative stress (OS) in several experimental models. Different noxious side effects related to those metabolites have also been observed upon estrogen therapy. In this sense, catecholestrogens seem to be implicated in tumoral and mutagenic process after long treatment with estrogens substitutive therapy.In our study, we have verified that 2OH and 4OH have antioxidant and cardioprotective effects against adriamycin (AD)-induced cardiomyopathy in ovariectomized (OVX) rats. Catecholestrogens diminished the lipid peroxides and carbonyl protein (CO) content, and different enzymes related to cellinjury (creatinine kinase, lactate dehydrogenase, aspartate aminotransferase, alanine aminotransferase) in cardiac tissue from OVX-, AD-, and OVX+AD-treated rats. All these changes were correlated to a recovery on reduced glutathione (GSH), glutathione peroxidase (GPx), superoxide dismutase (SOD) and catalase (CAT) in heart tissue.The present study showed that 2OH and 4OH reduced all the parameters related to OS, antioxidant depletion and cardiac injury in OVX rats treated or not with AD.
机译:雌激素衍生代谢产物或儿茶酚雌激素的治疗​​有益作用引起争议。这些分子是在基于17-β-雌二醇治疗的雌激素治疗期间产生的。 17-β-雌二醇的代谢在脑,肾或肝中进行,并引发不同的产物,例如2-和4-羟基雌二醇(2OH和4OH)。这些产品在几种实验模型中均显示出抗氧化应激(OS)的抗氧化性能。雌激素治疗后还观察到与这些代谢物相关的不同有害副作用。从这个意义上讲,儿茶酚雌激素似乎与长期使用雌激素替代疗法的肿瘤和致突变过程有关。 )大鼠。儿茶素雌激素可降低OVX,AD和OVX + AD治疗的大鼠心脏组织中脂质过氧化物和羰基蛋白(CO)的含量以及与细胞损伤相关的各种酶(肌酸酐激酶,乳酸脱氢酶,天冬氨酸转氨酶,丙氨酸转氨酶)。所有这些变化与心脏组织中还原型谷胱甘肽(GSH),谷胱甘肽过氧化物酶(GPx),超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的恢复有关。本研究表明2OH和4OH降低了与OS相关的所有参数或未接受AD治疗的OVX大鼠体内的抗氧化剂,抗氧化剂消耗和心脏损伤。

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