Brito Verônica B, Nascimento Leopoldo V M, Nunes Ramiro B, Moura Dinara J, Lago Pedro Dal, Saffi Jenifer
Laboratory of Genetic Toxicology, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.
Laboratory of Physiology, Federal University of Health Sciences of Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.
Toxicology. 2016 Aug 10;368-369:46-57. doi: 10.1016/j.tox.2016.08.017. Epub 2016 Aug 23.
Cancer treatment with Doxorubicin (DOX) is limited due its dose-dependent cardiotoxicity, mainly related to the oxidative stress production. In experimental models of DOX treatment exercise can be used as a beneficial adjuvant therapy. This work aimed to investigate the effects of exercise during pregnancy on DOX-induced cardiotoxicity in cardiomyocytes of progeny, examining the possible intergenerational cardioprotective effects of maternal exercise. For this purpose pregnant rats were divided in control and exercise groups and pre-treated during gestational days. Hearts of newborns were used to obtain a culture of cardiomyocytes to be treated with DOX for analyses of cell viability, apoptosis and necrosis; ROS production; DNA damage; SOD and CAT activities; and Sirt6 protein expression. The results showed that exercise during pregnancy induced an increase in the viability of neonatal cardiomyocytes and a decrease in DOX-induced apoptotic and necrotic death which were correlated to the decrease in ROS production and an increase in antioxidant defenses. Exercise also protected neonatal cardiomyocytes from DOX-induced DNA damage, demonstrating a reduction in the oxidative DNA breaks. Likewise, exercise induced an increase in expression of Sirt6 in neonatal cardiomyocytes. Therefore, these results demonstrate for the first time that exercise performed by mothers protects the neonatal heart against DOX-induced toxicity. Our data demonstrate the intergenerational effect of exercise in cardiomyocytes of progeny, where the modulation of oxidative stress through antioxidant enzymes, and DNA integrity via Sirt6, were induced due to exercise in mothers, increasing the resistance of the neonatal heart against DOX toxicity.
由于阿霉素(DOX)具有剂量依赖性心脏毒性,主要与氧化应激产生有关,其癌症治疗作用受到限制。在DOX治疗的实验模型中,运动可作为一种有益的辅助治疗方法。这项工作旨在研究孕期运动对后代心肌细胞中DOX诱导的心脏毒性的影响,探讨母体运动可能产生的代际心脏保护作用。为此,将怀孕大鼠分为对照组和运动组,并在孕期进行预处理。取新生大鼠的心脏以获得心肌细胞培养物,用DOX处理以分析细胞活力、凋亡和坏死情况;活性氧(ROS)产生;DNA损伤;超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性;以及沉默信息调节因子6(Sirt6)蛋白表达。结果表明,孕期运动可提高新生心肌细胞的活力,减少DOX诱导的凋亡和坏死性死亡,这与ROS产生减少和抗氧化防御增加有关。运动还可保护新生心肌细胞免受DOX诱导的DNA损伤,表明氧化DNA断裂减少。同样,运动可诱导新生心肌细胞中Sirt6表达增加。因此,这些结果首次证明母亲进行的运动可保护新生儿心脏免受DOX诱导的毒性。我们的数据证明了运动对后代心肌细胞的代际效应,即母亲运动通过抗氧化酶调节氧化应激,并通过Sirt6维持DNA完整性,从而增加新生儿心脏对DOX毒性的抵抗力。