Neuroanatomical basis for facilitation of hypothalamic-pituitary-adrenal responses to a novel stressor after chronic stress

• Published in: Neuroscience 1998-06, Vol.84 (4), p.1025-1039
• Main Authors: Bhatnagar, S., Dallman, M.
• Format: Article
• Language: English
• Subjects: Adrenocorticotropic Hormone - blood; adrenocorticotropin; amygdala; Anatomical correlates of behavior; Animals; Behavioral psychophysiology; Biological and medical sciences; Body Weight - physiology; Brain - physiology; Brain - ultrastructure; Chronic Disease; chronic stress; Cold Temperature; Corticosterone - blood; facilitation; Fundamental and applied biological sciences. Psychology; Hypothalamo-Hypophyseal System - pathology; Hypothalamo-Hypophyseal System - physiopathology; Immunohistochemistry; Male; paraventricular nucleus of the hypothalamus; paraventricular nucleus of the thalamus; Pituitary-Adrenal System - pathology; Pituitary-Adrenal System - physiopathology; Proto-Oncogene Proteins c-fos - biosynthesis; Psychology. Psychoanalysis. Psychiatry; Psychology. Psychophysiology; Rats; Rats, Sprague-Dawley; Restraint, Physical; Stress, Psychological - pathology; Stress, Psychological - physiopathology
• ISSN: 0306-4522; 1873-7544
• DOI: 10.1016/S0306-4522(97)00577-0

Animals exposed to chronic stress exhibit normal or enhanced hypothalamic-pituitary-adrenal responses to novel, acute stimuli despite the inhibitory endogenous corticosterond response to the chronic stressor. Prior stress is thought to induce a central facilitatory trace that, upon exposure to a novel stimulus, balances or overcomes the inhibitory effects of corticosterone. The neuroanatomical basis for this facilitation of hypothalamic-pituitary-adrenal responses is unknown. In this study, we first show increased adrenocorticotropin and corticosterone responses to the novel stressor of restraint in rats exposed to intermittent cold for seven days. We then compared numbers of Fos-immunoreactive cells in 26 sites in control and chronically stressed rats at various times after onset of a 30 min restraint. At 60 min, density of Fos-stained cells was significantly higher in chronically stressed than in control rats in the parabrachial/Kölliker-Fuse area, posterior paraventricular thalamus, central, basolateral and basomedial nuclei of the amygdala and parvocellular paraventricular hypothalamus. The posterior paraventricular nucleus of the thalamus receives projections from the parabrachial nucleus and projects heavily to the differentially stained subnuclei of the amygdala, which in turn project to the parvocellular paraventricular nucleus of the hypothalamus. We propose that increased activity in the parabrachial-posterior paraventricular thalamus-amygdala-parvocellular paraventricular hypothalamus underlies facilitation of the hypothalamic-pituitary-adrenal axis to novel stress in chronically stressed rats. We confirmed part of this proposal by showing that lesions of the posterior paraventricular nucleus of the thalamus increase adrenocorticotropin responses to restraint only in previously chronically stressed animals. This potential circuit provides a basis for further examination of the functional roles of these regions in stress-induced facilitation of hypothalamic-pituitary-adrenal activity.