Yin Dazhong, Chen Keji
Aging Biochemistry Laboratory, College of Life Sciences, Hunan Normal University, Changsha 410081, Hunan, China.
Exp Gerontol. 2005 Jun;40(6):455-65. doi: 10.1016/j.exger.2005.03.012.
Explanations on aging mechanisms have now become unexpectedly complicated. However, it is gradually accepted that 'senescence is a collective consequence of both inheritance and environment'. Based on the achievements of biological and medical research in related fields, we pinpoint in this review that although aging is mainly considered a physiological (non-pathological) process, the biochemical structure of aged organisms is deranged, or 'sick' at the molecular level. The free radical/glycation induced carbonyl stress, the key culprit to form crosslinks, has been identified to cause stable cyclic conjugates of mainly protein-based aggregates implying entropy increase (the Second Law of Thermodynamics) during aging. When combining such key aging processes with age pigment biochemistry, a general picture of aging process can be figured out, as the main clues and results are available. In this review we also propose for the first time that by focusing on 'process' rather than on 'causes' (damages), we can then get a clear view of aging mechanisms. Through rational thinking and critical analysis, we conclude that the accumulation of irreparable damages and alternations caused by spontaneous biological side-reactions seems to be the essential and profound nature of higher animals' aging mechanisms.
目前,关于衰老机制的解释已变得异常复杂。然而,“衰老乃遗传与环境共同作用的结果”这一观点正逐渐被人们所接受。基于相关领域生物学和医学研究的成果,我们在本综述中明确指出,尽管衰老主要被视为一个生理(非病理)过程,但在分子层面,衰老生物体的生化结构已紊乱,或者说已“患病”。自由基/糖基化诱导的羰基应激是形成交联的关键因素,已被证实会导致主要基于蛋白质的聚集体形成稳定的环状共轭物,这意味着衰老过程中熵增加(热力学第二定律)。当将这些关键的衰老过程与老年色素生物化学相结合时,鉴于主要线索和结果均已明晰,衰老过程的整体图景便可勾勒出来。在本综述中,我们还首次提出,通过关注“过程”而非“原因”(损伤),我们能够清晰地了解衰老机制。经过理性思考和批判性分析,我们得出结论,由自发生物副反应导致的不可修复损伤和改变的积累,似乎是高等动物衰老机制的本质和深层原因。