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Targeting tissue-specific metabolic signaling pathways in aging: the promise and limitations

机译:针对衰老的组织特异性代谢信号通路:前景和局限性

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摘要

It has been well established that most of the age-related diseases such as insulin resistance, type 2 diabetes, hypertension, cardiovascular disease, osteoporosis, and atherosclerosis are all closely related to metabolic dysfunction. On the other hand, interventions on metabolism such as calorie restriction or genetic manipulations of key metabolic signaling pathways such as the insulin and mTOR signaling pathways slow down the aging process and improve healthy aging. These findings raise an important question as to whether improving energy homeostasis by targeting certain metabolic signaling pathways in specific tissues could be an effective anti-aging strategy. With a more comprehensive understanding of the tissue-specific roles of distinct metabolic signaling pathways controlling energy homeostasis and the cross-talks between these pathways during aging may lead to the development of more effective therapeutic interventions not only for metabolic dysfunction but also for aging.
机译:众所周知,大多数与年龄有关的疾病,如胰岛素抵抗,2型糖尿病,高血压,心血管疾病,骨质疏松和动脉粥样硬化均与代谢功能障碍密切相关。另一方面,对代谢的干预(例如卡路里限制)或关键代谢信号途径(例如胰岛素和mTOR信号途径)的基因操作减缓了衰老过程并改善了健康衰老。这些发现提出了一个重要的问题,即通过靶向特定组织中的某些代谢信号通路来改善能量动态平衡是否可能是一种有效的抗衰老策略。对控制能量动态平衡的不同代谢信号通路的组织特异性作用有了更全面的了解,衰老过程中这些通路之间的相互影响可能导致开发出不仅针对代谢功能障碍而且对衰老更有效的治疗措施。

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