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7439947 
Journal Article 
The neuroendocrinology of stress and aging: The glucocorticoid cascade hypothesis 
Sapolsky, RM; Krey, LC; Mcewen, BS 
1986 
1 
Endocrine Reviews
ISSN: 0163-769X
EISSN: 1945-7189 
7 
3 
284-301 
English 
As RECENTLY as 1900, tuberculosis, influenza, and pneumonia were the leading causes of death in our country (1). For the most part, however, these infectious diseases, as well as those of poor hygiene or undernutrition, no longer plague us. Instead, we succumb most frequently to heart disease and cancer, diseases of slow degeneration (1). Most of all, unlike so many in the generations before us, we are in a position to age. Regardless of what else occurs, we age, we become more constrained by the discrepancy between what we were and what we have become, and each step becomes harder. The goal in the study of aging is not to halt the process, because we can no more be cured of aging than of birth. The goal, instead, is to slow and soften the sharpest edges of the biological unraveling that constitutes aging. Over the past 5 yr, we have examined some of the sharpest edges of the pathology of aging. We have studied the capacity of aged organisms to respond appropriately to stress and the capacity of stress to cumulatively damage aging tissue. © 1986 by The Endocrine Society. 
glucocorticoid; glucocorticoid receptor; aging; animal; biological model; cytology; feedback system; hippocampus; human; mental disease; nerve cell; pathophysiology; physiology; primate; rat; review; stress; Aging; Animal; Feedback; Glucocorticoids; Hippocampus; Human; Mental Disorders; Models, Neurological; Neurons; Primates; Rats; Receptors, Glucocorticoid; Stress; Support, Non-U.S. Gov't; Support, U.S. Gov't, P.H.S.