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超氧化物、一氧化氮和过氧亚硝酸盐在阿霉素体内外诱导细胞死亡中的作用

Role of superoxide, nitric oxide, and peroxynitrite in doxorubicin-induced cell death in vivo and in vitro.

作者信息

Mukhopadhyay Partha, Rajesh Mohanraj, Bátkai Sándor, Kashiwaya Yoshihiro, Haskó György, Liaudet Lucas, Szabó Csaba, Pacher Pál

机构信息

Section on Oxidative Stress and Tissue Injury, Laboratory of Physiological Studies, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, 5625 Fishers Lane, MSC-9413, Bethesda, MD 20892-9413, USA.

出版信息

Am J Physiol Heart Circ Physiol. 2009 May;296(5):H1466-83. doi: 10.1152/ajpheart.00795.2008. Epub 2009 Mar 13.

Abstract

Doxorubicin (DOX) is a potent available antitumor agent; however, its clinical use is limited because of its cardiotoxicity. Cell death is a key component in DOX-induced cardiotoxicity, but its mechanisms are elusive. Here, we explore the role of superoxide, nitric oxide (NO), and peroxynitrite in DOX-induced cell death using both in vivo and in vitro models of cardiotoxicity. Western blot analysis, real-time PCR, immunohistochemistry, flow cytometry, fluorescent microscopy, and biochemical assays were used to determine the markers of apoptosis/necrosis and sources of NO and superoxide and their production. Left ventricular function was measured by a pressure-volume system. We demonstrated increases in myocardial apoptosis (caspase-3 cleavage/activity, cytochrome c release, and TUNEL), inducible NO synthase (iNOS) expression, mitochondrial superoxide generation, 3-nitrotyrosine (NT) formation, matrix metalloproteinase (MMP)-2/MMP-9 gene expression, poly(ADP-ribose) polymerase activation [without major changes in NAD(P)H oxidase isoform 1, NAD(P)H oxidase isoform 2, p22(phox), p40(phox), p47(phox), p67(phox), xanthine oxidase, endothelial NOS, and neuronal NOS expression] and decreases in myocardial contractility, catalase, and glutathione peroxidase activities 5 days after DOX treatment to mice. All these effects of DOX were markedly attenuated by peroxynitrite scavengers. Doxorubicin dose dependently increased mitochondrial superoxide and NT generation and apoptosis/necrosis in cardiac-derived H9c2 cells. DOX- or peroxynitrite-induced apoptosis/necrosis positively correlated with intracellular NT formation and could be abolished by peroxynitrite scavengers. DOX-induced cell death and NT formation were also attenuated by selective iNOS inhibitors or in iNOS knockout mice. Various NO donors when coadministered with DOX but not alone dramatically enhanced DOX-induced cell death with concomitant increased NT formation. DOX-induced cell death was also attenuated by cell-permeable SOD but not by cell-permeable catalase, the xanthine oxidase inhibitor allopurinol, or the NADPH oxidase inhibitors apocynine or diphenylene iodonium. Thus, peroxynitrite is a major trigger of DOX-induced cell death both in vivo and in vivo, and the modulation of the pathways leading to its generation or its effective neutralization can be of significant therapeutic benefit.

摘要

阿霉素(DOX)是一种有效的抗肿瘤药物;然而,由于其心脏毒性,其临床应用受到限制。细胞死亡是DOX诱导的心脏毒性的关键组成部分,但其机制尚不清楚。在这里,我们使用体内和体外心脏毒性模型来探讨超氧化物、一氧化氮(NO)和过氧亚硝酸盐在DOX诱导的细胞死亡中的作用。采用蛋白质免疫印迹分析、实时聚合酶链反应、免疫组织化学、流式细胞术、荧光显微镜检查和生化分析来确定凋亡/坏死标志物以及NO和超氧化物的来源及其产生情况。通过压力-容积系统测量左心室功能。我们证明,在给小鼠注射DOX 5天后,心肌凋亡(半胱天冬酶-3切割/活性、细胞色素c释放和TUNEL)、诱导型一氧化氮合酶(iNOS)表达、线粒体超氧化物生成、3-硝基酪氨酸(NT)形成、基质金属蛋白酶(MMP)-2/MMP-9基因表达、聚(ADP-核糖)聚合酶激活[烟酰胺腺嘌呤二核苷酸磷酸(NAD(P)H)氧化酶同工型1、NAD(P)H氧化酶同工型2、p22(phox)、p40(phox)、p47(phox)、p67(phox)、黄嘌呤氧化酶、内皮型一氧化氮合酶和神经元型一氧化氮合酶表达无重大变化]增加,心肌收缩力、过氧化氢酶和谷胱甘肽过氧化物酶活性降低。DOX的所有这些作用均被过氧亚硝酸盐清除剂显著减弱。阿霉素剂量依赖性地增加心脏来源的H9c2细胞中的线粒体超氧化物和NT生成以及凋亡/坏死。DOX或过氧亚硝酸盐诱导的凋亡/坏死与细胞内NT形成呈正相关,并且可被过氧亚硝酸盐清除剂消除。DOX诱导的细胞死亡和NT形成在选择性iNOS抑制剂或iNOS基因敲除小鼠中也减弱。各种NO供体与DOX共同给药(而非单独给药)时会显著增强DOX诱导的细胞死亡,并伴随NT形成增加。DOX诱导的细胞死亡也被细胞可渗透的超氧化物歧化酶减弱,但未被细胞可渗透的过氧化氢酶、黄嘌呤氧化酶抑制剂别嘌呤醇或NADPH氧化酶抑制剂夹竹桃麻素或二苯碘鎓减弱。因此,过氧亚硝酸盐是DOX在体内和体外诱导细胞死亡的主要触发因素,调节导致其产生的途径或有效中和它可能具有显著的治疗益处。

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