Fannin Jacqueline, Rice Kevin M, Thulluri Srininvas, Arvapalli Ravi Kumar, Wehner Paulette, Blough Eric R
Department of Pharmacology, Physiology, and Toxicology, Joan C. Edwards School of Medicine, Marshall University, USA ; Center for Diagnostic Nanosystems, Marshall University, Huntington WV, USA.
Department of Internal Medicine, Joan C. Edwards School of Medicine, Marshall University, Huntington WV, USA ; Center for Diagnostic Nanosystems, Marshall University, Huntington WV, USA.
Open Cardiovasc Med J. 2013 Nov 29;7:113-21. doi: 10.2174/1874192401307010113. eCollection 2013.
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.
近期研究表明,氧化亚硝化应激可能在与年龄相关的心血管疾病中发挥作用。然而,使用老年雌性啮齿动物模型进行的研究有限。在本研究中,我们检查了从6个月、26个月和30个月大的雌性Fischer 344/Nnia x Brown Norway/BiNia(F344xBN)大鼠获取的心脏,以研究衰老如何影响心脏氧化亚硝化应激水平和细胞凋亡。与6个月大雌性大鼠的心脏相比,30个月大心脏中的氧化应激(超氧阴离子和4-羟基壬烯醛)和亚硝化应激(蛋白质亚硝化)标志物分别增加了180±17%、110±3%和14±2%。与氧化亚硝化应激的这些变化一致,衰老还与末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)阳性心肌细胞数量增加、Bax/Bcl-2比值改变以及caspase-3裂解增加有关。回归分析表明,氧化亚硝化应激的年龄相关变化标志物与凋亡信号变化之间存在显著相关性。这项描述性研究的结果表明,衰老的F344xBN雌性心脏中线粒体介导的细胞凋亡增加可能与氧化亚硝化应激增加有关。