DEPRESSION GETS OLD FAST: DO STRESS AND DEPRESSION ACCELERATE CELL AGING?

被引:226
作者
Wolkowitz, Owen M. [1 ]
Epel, Elissa S. [1 ]
Reus, Victor I. [1 ]
Mellon, Synthia H. [2 ]
机构
[1] Univ Calif San Francisco, Sch Med, Dept Psychiat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Sch Med, Dept OB GYN & Reprod Sci, San Francisco, CA USA
关键词
depression; stress; aging; cortisol; BDNF; DHEA; telomeres; oxidation; inflammation; allopregnanolone; SEROTONIN REUPTAKE INHIBITORS; PRO-INFLAMMATORY CYTOKINES; UNIPOLAR MAJOR DEPRESSION; INDUCED OXIDATIVE STRESS; GLUCOCORTICOID-RECEPTOR; NEUROTROPHIC FACTOR; CARDIOVASCULAR-DISEASE; TELOMERE LENGTH; NEUROACTIVE STEROIDS; HIPPOCAMPAL NEUROGENESIS;
D O I
10.1002/da.20686
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Depression has been likened to a state of "accelerated aging," and depressed individuals have a higher incidence of various diseases of aging, such as cardiovascular and cerebro vascular diseases, metabolic syndrome, and dementia. Chronic exposure to certain interlinked biochemical pathways that mediate stress-related depression may contribute to "accelerated aging," cell damage, and certain comorbid medical illnesses. Biochemical mediatory explored in this theoretical review include the hypothalamic-pituitary-adrenal axis (e.g., hyperor hypoactivation of glucocorticoid receptors), neurosteroids, such as dehydroepiandrosterone and allopregnanolone, brain-derived neurotrophic factor excitotoxicity, oxidative and inflammatory stress, and disturbances of the telomere/telomerase maintenance system. A better appreciation of the role of these mediators in depressive illness could lead to refined models of depression, to a re-conceptualization of depression as a whole body disease rather than just a "mental illness," and to the rational development of new classes of medications to treat depression and its related medical comorbidities. Depression and Anxiety 27:327-338, 2010. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:327 / 338
页数:12
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