Department of Biological Sciences, Missouri University of Science and Technology, Rolla, MO, USA.
Mech Ageing Dev. 2013 Sep;134(9):373-80. doi: 10.1016/j.mad.2013.07.001. Epub 2013 Jul 18.
Understanding the trade-offs between organisms' life history traits has been a major goal of physiology, ecology and evolution. In the last few decades, two types of intra-specific studies have highlighted the trade-off between growth and longevity. First, diet restriction (DR), as an environmental intervention, has been shown to suppress growth and extend the lifespan of a broad range of animals. Second, genetic studies have also shown that mice, whose growth hormone function is genetically modified (GM), grow slower and live longer than their wild-type siblings. Despite a wealth of empirical data, still largely missing is a theoretical framework that specifies and makes quantitative predictions on this trade-off. Here, I present a mechanistic model based on the principles of energy conservation. The model quantifies explicitly how DR and GM alter the animal's energy budget, and channel metabolic energy to somatic maintenance by suppressing growth, thereby extending lifespan. Data from a diverse set of empirical studies on small rodents supports the predictions of the model. More importantly, the model reveals that although DR and GM are two different methods to extend lifespan, i.e., environmental vs. genetic, the underlying mechanisms of them are the same from the energetic viewpoint.
理解生物体生活史特征之间的权衡一直是生理学、生态学和进化的主要目标。在过去的几十年中,两种类型的种内研究强调了生长和长寿之间的权衡。首先,饮食限制(DR)作为一种环境干预手段,已被证明可以抑制生长并延长广泛动物的寿命。其次,遗传研究也表明,生长激素功能发生遗传修饰(GM)的小鼠比其野生型兄弟姐妹生长缓慢且寿命更长。尽管有大量的经验数据,但仍缺乏一个理论框架来具体说明并对这种权衡进行定量预测。在这里,我提出了一个基于能量守恒原理的机械模型。该模型明确地量化了 DR 和 GM 如何通过抑制生长来改变动物的能量预算,并将代谢能量输送到体细胞维持,从而延长寿命。来自小型啮齿动物的一系列不同的经验研究的数据支持该模型的预测。更重要的是,该模型表明,尽管 DR 和 GM 是延长寿命的两种不同方法,即环境与遗传,但从能量角度来看,它们的潜在机制是相同的。