Jacqueline Fannin, Kevin M Rice, Srininvas Thulluri, Ravi Kumar Arvapalli, Paulette Wehner, Eric R Blough
{"title":"The Effects of Aging on Indices of Oxidative Stress and Apoptosis in the Female Fischer 344/Nnia X Brown Norway/BiNia Rat Heart.","authors":"Jacqueline Fannin, Kevin M Rice, Srininvas Thulluri, Ravi Kumar Arvapalli, Paulette Wehner, Eric R Blough","doi":"10.2174/1874192401307010113","DOIUrl":null,"url":null,"abstract":"<p><p>Oxidative-nitrosative stress may play a role in age-associated cardiovascular disease as implied by recent studies.However, limited research has been conducted using aged female rodent models. In this study, we examined hearts obtained from 6-, 26-, and 30-month old female Fischer 344/Nnia x Brown Norway/BiNia (F344xBN) rats in order to examine how aging affects levels of cardiac oxidative-nitrosative stress and apoptosis. Oxidative (superoxide anion and 4-HNE) and nitrosative (protein nitrosylation) stress markers were increased 180 ± 17 %, 110 ± 3 %, and 14 ± 2 %, respectively in 30-month hearts compared to the hearts of 6-month female rats. Coincident with these changes in oxidative-nitrosative stress, aging was also found to be associated with increases in the number of Tdt-mediated dUTP nick labeling (TUNEL)-positive cardiomyocytes, alterations in the Bax/Bcl-2 ratio, and elevated cleavage of caspase-3. Regression analysis demonstrates significant correlation in the age-associated changes markers of oxidative-nitrosative stress with changes in apoptotic signaling. The findings from this descriptive study imply that age-associated increases in mitochondrial-mediated apoptosis may be associated with the increase in oxidative-nitrosative stress in the aging F344xBN female heart. </p>","PeriodicalId":504447,"journal":{"name":"The Open Cardiovascular Medicine Journal","volume":"7 ","pages":"113-21"},"PeriodicalIF":0.0000,"publicationDate":"2013-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/c0/23/TOCMJ-7-113.PMC3866772.pdf","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Open Cardiovascular Medicine Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1874192401307010113","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2013/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10
Abstract
Oxidative-nitrosative stress may play a role in age-associated cardiovascular disease as implied by recent studies.However, limited research has been conducted using aged female rodent models. In this study, we examined hearts obtained from 6-, 26-, and 30-month old female Fischer 344/Nnia x Brown Norway/BiNia (F344xBN) rats in order to examine how aging affects levels of cardiac oxidative-nitrosative stress and apoptosis. Oxidative (superoxide anion and 4-HNE) and nitrosative (protein nitrosylation) stress markers were increased 180 ± 17 %, 110 ± 3 %, and 14 ± 2 %, respectively in 30-month hearts compared to the hearts of 6-month female rats. Coincident with these changes in oxidative-nitrosative stress, aging was also found to be associated with increases in the number of Tdt-mediated dUTP nick labeling (TUNEL)-positive cardiomyocytes, alterations in the Bax/Bcl-2 ratio, and elevated cleavage of caspase-3. Regression analysis demonstrates significant correlation in the age-associated changes markers of oxidative-nitrosative stress with changes in apoptotic signaling. The findings from this descriptive study imply that age-associated increases in mitochondrial-mediated apoptosis may be associated with the increase in oxidative-nitrosative stress in the aging F344xBN female heart.
衰老对雌性Fischer 344/Nnia X Brown Norway/BiNia大鼠心脏氧化应激及细胞凋亡指标的影响。
最近的研究表明,氧化-亚硝化应激可能在与年龄相关的心血管疾病中起作用。然而,使用老年雌性啮齿动物模型进行的研究有限。在这项研究中,我们检查了6、26和30个月大的雌性Fischer 344/Nnia x Brown Norway/BiNia (f344 × bn)大鼠的心脏,以研究衰老如何影响心脏氧化亚硝化应激和凋亡水平。与6月龄雌性大鼠相比,30月龄雌性大鼠心脏的氧化(超氧阴离子和4-HNE)和亚硝化(蛋白质亚硝基化)应激标志物分别增加180±17%、110±3%和14±2%。与氧化亚硝化应激的这些变化相一致的是,衰老还被发现与tdt介导的dUTP nick labeling (TUNEL)阳性心肌细胞数量的增加、Bax/Bcl-2比值的改变以及caspase-3切割水平的升高有关。回归分析显示,氧化亚硝化应激的年龄相关变化标志物与凋亡信号的变化有显著相关性。这项描述性研究的结果表明,年龄相关的线粒体介导的细胞凋亡的增加可能与衰老的f344 × bn女性心脏中氧化亚硝化应激的增加有关。