Individual differences in cortisol secretory patterns in the wild baboon: role of negative feedback sensitivity.

It was previously shown that rank-related differences in adrenocortical function existed among the males of a troop of olive baboons living in their natural habitat in East Africa. High-ranking males, by the criterion of reproductive activity, had significantly lower cortisol titers than those of subordinates, when measured immediately after immobilization with anesthetic. However, high-ranking males elevated titers rapidly during the early period of immobilization stress, attaining titers equal to those of subordinates at 60 min. The present study replicates these rank differences and provides possible endocrine mechanisms underlying them. Males with low basal titers (predominantly high-ranking males) had the fastest and most extreme suppressions of circulating cortisol titers after dexamethasone administration. However, they had cortisol clearance rates similar to those of individuals with high initial cortisol titers. These data suggest that the rank-related variance in basal cortisol levels is attributable to differential sensitivity to negative feedback regulation. Males who elevated cortisol titer most rapidly during the early poststress period (again, predominantly high-ranking males) had adrenals no more responsive to an ACTH challenge than those of remaining subjects. This suggests that a rapid adrenocortical secretory response during stress is not attributable to enhanced adrenal sensitivity to ACTH, but rather to an accelerated secretion of ACTH by the pituitary gland.

[1]  J. Holaday,et al.  Plasma Testosterone, Dominance Rank and Aggressive Behaviour in Male Rhesus Monkeys , 1971, Nature.

[2]  W. R. Bulter,et al.  Surgical disconnection of the medial basal hypothalamus and pituitary function in the rhesus monkey. II. GH and cortisol secretion. , 1975, Endocrinology.

[3]  G. Riegle,et al.  Chronic and acute dexamethasone suppression of stress activation of the adrenal cortex in young and aged rats. , 1972, Neuroendocrinology.

[4]  C. Coe,et al.  Social status constrains the stress response in the squirrel monkey , 1979, Physiology & Behavior.

[5]  C. Coe,et al.  The physiological response to group formation in adult male squirrel monkeys , 1978, Psychoneuroendocrinology.

[6]  Robert M. Sapolsky,et al.  Endocrine aspects of social instability in the olive baboon (Papio anubis) , 1983, American journal of primatology.

[7]  Robert M. Sapolsky,et al.  The endocrine stress-response and social status in the wild baboon , 1982, Hormones and Behavior.

[8]  B. McEwen,et al.  The adrenocorticol stress-response in the aged male rat: Impairment of recovery from stress , 1983, Experimental Gerontology.

[9]  R. Rose,et al.  Consequences of Social Conflict on Plasma Testosterone Levels in Rhesus Monkeys , 1975, Psychosomatic medicine.

[10]  R. Vigersky,et al.  Glucocorticoid hormone resistance during primate evolution: receptor-mediated mechanisms. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[11]  M. Golub,et al.  Plasma cortisol levels and dominance in peer groups of rhesus monkey weanlings , 1979, Hormones and Behavior.

[12]  J. Ottenweller,et al.  Adrenal innervation may be an extrapituitary mechanism able to regulate adrenocortical rhythmicity in rats. , 1982, Endocrinology.

[13]  B. McEwen,et al.  Corticosterone receptors decline in a site-specific manner in the aged rat brain , 1983, Brain Research.

[14]  D. Krieger Cushing's syndrome. , 1982, Monographs on endocrinology.

[15]  J. Altmann,et al.  Observational study of behavior: sampling methods. , 1974, Behaviour.