Ramadori Giorgio, Coppari Roberto
Department of Internal Medicine, Division of Hypothalamic Research, The University of Texas Southwestern Medical Center, Dallas, 75390, USA.
Aging (Albany NY). 2011 Mar;3(3):325-8. doi: 10.18632/aging.100311.
In virtually all organisms, life expectancy is profoundly affected by caloric intake. For example, dietary restriction (DR; a feeding regimen of fewer calories compared to the ad libitum level without causing malnutrition) has been shown to lengthen, whereas hypercaloric (HC) diet feeding to shorten, lifespan. Recent findings in invertebrates indicate that specialized groups of cells (e.g.: metabolic-sensing neurons) detect changes in caloric intake and convey energy-status-variation signals to other cells in the body to regulate lifespan. In mammals, whether metabolic-sensing neurons govern aging in a cell-non-autonomous fashion is unknown. Yet, this is a captivating and testable hypothesis.
几乎在所有生物体中,预期寿命都受到热量摄入的深刻影响。例如,饮食限制(DR;一种与随意进食水平相比热量摄入较少但不会导致营养不良的喂养方案)已被证明可以延长寿命,而高热量(HC)饮食喂养则会缩短寿命。最近在无脊椎动物中的研究结果表明,特定的细胞群(例如:代谢感知神经元)会检测热量摄入的变化,并将能量状态变化信号传递给身体中的其他细胞以调节寿命。在哺乳动物中,代谢感知神经元是否以细胞非自主方式控制衰老尚不清楚。然而,这是一个引人入胜且可检验的假设。