Suppr超能文献

慢性 Akt 激活加剧衰老诱导的心肌肥厚和心肌收缩功能障碍:自噬的作用。

Chronic Akt activation accentuates aging-induced cardiac hypertrophy and myocardial contractile dysfunction: role of autophagy.

机构信息

Center for Cardiovascular Research and Alternative Medicine, University of Wyoming College of Health Sciences, Laramie, WY 82071, USA.

出版信息

Basic Res Cardiol. 2011 Nov;106(6):1173-91. doi: 10.1007/s00395-011-0222-8. Epub 2011 Sep 9.

Abstract

Aging is often accompanied with geometric and functional changes in the heart, although the underlying mechanisms remain unclear. Recent evidence has described a potential role of Akt and autophagy in aging-associated organ deterioration. This study was to examine the impact of cardiac-specific Akt activation on aging-induced cardiac geometric and functional changes and underlying mechanisms involved. Cardiac geometry, contractile and intracellular Ca(2+) properties were evaluated using echocardiography, edge-detection and fura-2 techniques. Level of insulin signaling and autophagy was evaluated by western blot. Our results revealed cardiac hypertrophy (enlarged chamber size, wall thickness, myocyte cross-sectional area), fibrosis, decreased cardiac contractility, prolonged relengthening along with compromised intracellular Ca(2+) release and clearance in aged (24-26 month-old) mice compared with young (3-4 month-old) mice, the effects of which were accentuated by chronic Akt activation. Aging enhanced Akt and mTOR phosphorylation while reducing that of PTEN, AMPK and ACC with a more pronounced response in Akt transgenic mice. GSK3β phosphorylation and eNOS levels were unaffected by aging or Akt overexpression. Levels of beclin-1, Atg5 and LC3-II-to-LC3-I ratio were decreased in aged hearts, the effect of which with the exception of Atg 5 was exacerbated by Akt overactivation. Levels of p62 were significantly enhanced in aged mice with a more pronounced increase in Akt mice. Neither aging nor Akt altered β-glucuronidase activity and cathepsin B although aging reduced LAMP1 level. In addition, rapamycin reduced aging-induced cardiomyocyte contractile and intracellular Ca(2+) dysfunction while Akt activation suppressed autophagy in young but not aged cardiomyocytes. In conclusion, our data suggest that Akt may accentuate aging-induced cardiac geometric and contractile defects through a loss of autophagic regulation.

摘要

衰老通常伴随着心脏的几何和功能变化,尽管其潜在机制尚不清楚。最近的证据描述了 Akt 和自噬在与衰老相关的器官恶化中的潜在作用。本研究旨在探讨心脏特异性 Akt 激活对衰老引起的心脏几何和功能变化的影响及其潜在机制。使用超声心动图、边缘检测和 fura-2 技术评估心脏几何形状、收缩和细胞内 Ca(2+)特性。通过 Western blot 评估胰岛素信号和自噬水平。我们的结果显示,与年轻(3-4 个月大)小鼠相比,老年(24-26 个月大)小鼠的心脏出现肥大(心室腔增大、壁增厚、心肌细胞横截面积增大)、纤维化、收缩力下降、再缩短延长以及细胞内 Ca(2+)释放和清除受损,这些效应在慢性 Akt 激活的情况下更为明显。衰老增强了 Akt 和 mTOR 的磷酸化,同时降低了 PTEN、AMPK 和 ACC 的磷酸化,Akt 转基因小鼠的反应更为明显。GSK3β 磷酸化和 eNOS 水平不受衰老或 Akt 过表达的影响。衰老导致心脏中 beclin-1、Atg5 和 LC3-II-to-LC3-I 比值降低,除了 Atg5 之外,Akt 过激活进一步加剧了这种效应。p62 的水平在老年小鼠中显著增加,在 Akt 小鼠中增加更为明显。衰老和 Akt 均未改变β-葡萄糖醛酸酶活性和组织蛋白酶 B,尽管衰老降低了 LAMP1 水平。此外,雷帕霉素减轻了衰老引起的心肌细胞收缩和细胞内 Ca(2+)功能障碍,而 Akt 激活抑制了年轻但不是老年心肌细胞中的自噬。综上所述,我们的数据表明,Akt 可能通过失去自噬调节来加剧衰老引起的心脏几何和收缩缺陷。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验