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Calorie restriction can reverse, as well as prevent, aging cardiomyopathy

机译:热量限制可以逆转并预防衰老的心肌病

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摘要

Calorie restriction (CR) is the most widely studied intervention protecting from the adverse effects of aging. Almost all prior studies have examined the effects of CR initiated in young animals. Studies examining the effects of CR on development of aging cardiomyopathy found only partial prevention. The major goal of this study was to determine whether CR initiated after aging cardiomyopathy developed could reverse the cardiomyopathy. Aging cardiomyopathy in 2-year-old mice was characterized by reduced left ventricular (LV) function, cardiac hypertrophy, and increased cardiac apoptosis and fibrosis. When short-term (2 months) CR was initiated after aging cardiomyopathy developed in 20-month-old mice, the decrease in cardiac function, and increases in LV weight, myocardial fibrosis and apoptosis were reversed, such that the aging hearts in these mice were indistinguishable from those of young mice or mice where CR was initiated in young mice. If apoptosis was the mechanism for protecting against aging cardiomyopathy, then total myocyte numbers should have reverted to normal with CR, but did not. However, the alterations in cytoskeletal proteins, which contribute to aging cardiomyopathy, were no longer observed with CR. This is the first study to demonstrate complete prevention of aging cardiomyopathy by CR and, more importantly, that instituting this intervention even later in life can rapidly correct aging cardiomyopathy, which could have important therapeutic implications.
机译:卡路里限制(CR)是研究最广泛的干预措施,可防止衰老。几乎所有先前的研究都检查了CR对幼小动物的影响。研究CR对衰老型心肌病发展的影响的研究仅发现了部分预防措施。这项研究的主要目的是确定在老化性心肌病发生后启动CR是否可以逆转心肌病。 2岁小鼠的老化性心肌病的特征在于左心室(LV)功能降低,心脏肥大以及心脏凋亡和纤维化增加。当在20个月大的小鼠中出现老化性心肌病后开始短期(2个月)CR时,心功能下降,LV重量增加,心肌纤维化和细胞凋亡被逆转,从而使这些小鼠的心脏老化与年轻小鼠或在年轻小鼠中引发CR的小鼠没有区别。如果凋亡是防止衰老型心肌病的机制,那么CR可以使总的心肌细胞数量恢复正常,但事实并非如此。然而,在CR中不再观察到导致衰老性心肌病的细胞骨架蛋白的改变。这是第一个通过CR完全预防衰老型心肌病的研究,更重要的是,即使在生命的晚些时候采取这种干预措施也可以迅速纠正衰老型心肌病,这可能具有重要的治疗意义。

著录项

  • 来源
    《AGE》 |2013年第6期|2177-2182|共6页
  • 作者单位

    Department of Cell Biology and Molecular Medicine Cardiovascular Research Institute UMDNJ-New Jersey Medical School">(1);

    Department of Cell Biology and Molecular Medicine Cardiovascular Research Institute UMDNJ-New Jersey Medical School">(1);

    Department of Cell Biology and Molecular Medicine Cardiovascular Research Institute UMDNJ-New Jersey Medical School">(1);

    Department of Cell Biology and Molecular Medicine Cardiovascular Research Institute UMDNJ-New Jersey Medical School">(1);

    Department of Cell Biology and Molecular Medicine Cardiovascular Research Institute UMDNJ-New Jersey Medical School">(1);

    Department of Cell Biology and Molecular Medicine Cardiovascular Research Institute UMDNJ-New Jersey Medical School">(1);

    Department of Cell Biology and Molecular Medicine Cardiovascular Research Institute UMDNJ-New Jersey Medical School">(1);

    Department of Cell Biology and Molecular Medicine Cardiovascular Research Institute UMDNJ-New Jersey Medical School">(1);

    Department of Cell Biology and Molecular Medicine Cardiovascular Research Institute UMDNJ-New Jersey Medical School">(1);

    Department of Cell Biology and Molecular Medicine Cardiovascular Research Institute UMDNJ-New Jersey Medical School">(1);

    Department of Cell Biology and Molecular Medicine Cardiovascular Research Institute UMDNJ-New Jersey Medical School">(1);

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Calorie restriction; Aging; Cardiomyopathy; Apoptosis; Myocyte loss;

    机译:热量限制;老化;心肌病;细胞凋亡;心肌细胞丢失;

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