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单宁酸可能改善阿霉素诱导的大鼠脾脏氧化应激参数变化。

Tannic acid may ameliorate doxorubicin-induced changes in oxidative stress parameters in rat spleen.

作者信息

Kizir Duygu, Karaman Melike, Ceylan Hamid

机构信息

Department of Molecular Biology and Genetics, Faculty of Science, Atatürk University, 25240, Erzurum, Turkey.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2023 Dec;396(12):3605-3613. doi: 10.1007/s00210-023-02563-w. Epub 2023 Jun 5.

Abstract

Doxorubicin (DOX) is a potent and broad-spectrum drug widely used in the treatment of cancer. However, the toxicity and side effects of DOX on various organs limit its clinical use. Approaches using natural antioxidants with these drugs have the potential to alleviate negative side effects. The aim of this study was to investigate the potential protective effect of tannic acid, a polyphenolic compound found naturally in plants, against DOX-induced spleen toxicity. Expression levels of Alox5, Inos, IL-6, Tnf-α, Casp-3, Bax, SOD, GST, CAT and GPx genes were determined using cDNAs obtained from spleen tissues of rats treated with DOX, tannic acid and both. In addition, SOD, CAT, GPx and GST enzyme activities, and GSH and MDA levels were measured in tissues. In the spleen tissues, DOX caused a decrease in the level of GSH and an increase in the level of MDA. In addition, it was determined that DOX had a suppressive effect on CAT, GST, SOD and GPx mRNA levels and its enzyme activities, which are antioxidant system components. The mRNA expression levels of proinflammatory cytokine markers, apoptotic genes, and some factors involved in cell metabolism showed a change compared to the control after DOX application. However, as a result of tannic acid treatment with DOX, these changes approached the values of the control group. The findings showed that tannic acid had a protective effect on the changes in the oxidative stress and inflammation system in the rat spleen as a result of the application of tannic acid together with DOX.

摘要

阿霉素(DOX)是一种强效的广谱药物,广泛用于癌症治疗。然而,DOX对各种器官的毒性和副作用限制了其临床应用。将天然抗氧化剂与这些药物联合使用的方法有可能减轻负面副作用。本研究的目的是探讨植物中天然存在的多酚化合物单宁酸对DOX诱导的脾脏毒性的潜在保护作用。使用从用DOX、单宁酸以及两者处理的大鼠脾脏组织中获得的cDNA,测定Alox5、Inos、IL-6、Tnf-α、Casp-3、Bax、SOD、GST、CAT和GPx基因的表达水平。此外,还测量了组织中的SOD、CAT、GPx和GST酶活性以及GSH和MDA水平。在脾脏组织中,DOX导致GSH水平降低和MDA水平升高。此外,还确定DOX对抗氧化系统成分CAT、GST、SOD和GPx的mRNA水平及其酶活性具有抑制作用。与对照组相比,DOX应用后促炎细胞因子标志物、凋亡基因和一些参与细胞代谢的因子的mRNA表达水平发生了变化。然而,DOX与单宁酸联合处理后,这些变化接近对照组的值。研究结果表明,单宁酸与DOX联合应用对大鼠脾脏氧化应激和炎症系统的变化具有保护作用。

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