Garfinkel D
Med Hypotheses. 1986 Feb;19(2):117-37. doi: 10.1016/0306-9877(86)90053-8.
A review of the literature suggests that an intracellular zinc deficiency may be the primary cause of the aging process. Zinc-metalloenzymes play an important role in many aspects of cellular metabolism including DNA replication, repair and transcription. The main enzymes affected by zinc deficiency may be specific for each cell type. Depending on which zinc enzymes are "overvulnerable", zinc deficiency may result in accumulation of useless (or toxic) materials, malproduction of essential proteins, a neoplastic change or cell death, thus explaining the variability in aging patterns in different cell types. There is no simple and reliable index of zinc status in humans and a therapeutic trial may be needed to establish zinc deficiency. Finding a zinc-compound which can enter the cell and avoid the development of intracellular zinc deficiency may retard the aging process and postpone age-related diseases.
文献综述表明,细胞内锌缺乏可能是衰老过程的主要原因。锌金属酶在细胞代谢的许多方面发挥着重要作用,包括DNA复制、修复和转录。受锌缺乏影响的主要酶可能因细胞类型而异。根据哪些锌酶“过度脆弱”,锌缺乏可能导致无用(或有毒)物质的积累、必需蛋白质的产生不足、肿瘤性变化或细胞死亡,从而解释了不同细胞类型衰老模式的变异性。人类锌状态没有简单可靠的指标,可能需要进行治疗试验来确定锌缺乏。找到一种能够进入细胞并避免细胞内锌缺乏发展的锌化合物,可能会延缓衰老过程并推迟与年龄相关的疾病。