Verhoeven Josine E, Révész Dóra, Wolkowitz Owen M, Penninx Brenda W J H
Department of Psychiatry and EMGO Institute for Health and Care Research, VU University Medical Centre, Amsterdam, The Netherlands.
Bioessays. 2014 Oct;36(10):968-78. doi: 10.1002/bies.201400068. Epub 2014 Aug 20.
Depression might be associated with accelerated cellular aging. However, does this result in an irreversible state or is the body able to slow down or recover from such a process? Telomeres are DNA-protein complexes that protect the ends of chromosomes and generally shorten with age; and therefore index cellular aging. The majority of studies indicate that persons with depression have shorter leukocyte telomeres than similarly aged non-depressed persons, which may contribute to the observed unfavorable somatic health outcomes in the depressed population. Some small-scale preliminary studies raise the possibility that behavioral or pharmacological interventions may either slow down or else reverse this accelerated telomere shortening, possibly through increasing the activity of the telomere-lengthening enzyme telomerase. This paper covers the current state of evidence in the relationship between depression and the telomere-telomerase system and debates whether depression-related cellular aging should be considered a reversible process or permanent damage.
抑郁症可能与细胞衰老加速有关。然而,这会导致一种不可逆的状态,还是身体能够减缓或从这样一个过程中恢复过来呢?端粒是一种DNA - 蛋白质复合物,可保护染色体末端,并且通常会随着年龄的增长而缩短;因此可作为细胞衰老的指标。大多数研究表明,抑郁症患者的白细胞端粒比年龄相仿的非抑郁症患者更短,这可能是抑郁症患者出现不良躯体健康状况的原因之一。一些小规模的初步研究提出了这样一种可能性,即行为或药物干预可能会减缓或逆转这种加速的端粒缩短,可能是通过增加端粒延长酶端粒酶的活性来实现。本文涵盖了抑郁症与端粒 - 端粒酶系统之间关系的当前证据状况,并探讨了与抑郁症相关的细胞衰老应被视为一个可逆过程还是永久性损伤。