Medial prefrontal cortex activity can disrupt the expression of stress response habituation

• Published in: Neuroscience 2010-07, Vol.168 (3), p.744-756
• Main Authors: Weinberg, M.S, Johnson, D.C, Bhatt, A.P, Spencer, R.L
• Format: Article
• Language: English
• Subjects: Adaptation, Physiological; Adaptations; Animals; Biological and medical sciences; c-fos; corticosterone; Corticosterone - metabolism; Fundamental and applied biological sciences. Psychology; habituation; Habituation, Psychophysiologic; HPA axis; Hypothalamo-Hypophyseal System - physiopathology; Male; Muscimol - pharmacology; Neurology; PFC; Picrotoxin - pharmacology; Pituitary-Adrenal System - physiopathology; Prefrontal Cortex - drug effects; Prefrontal Cortex - metabolism; Prefrontal Cortex - physiopathology; Proto-Oncogene Proteins c-fos - biosynthesis; Proto-Oncogene Proteins c-fos - genetics; Rats; Rats, Sprague-Dawley; Restraint, Physical; RNA, Messenger - biosynthesis; stress; Stress, Psychological - physiopathology; Stress, Psychological - psychology; Vertebrates: nervous system and sense organs
• ISSN: 0306-4522; 1873-7544
• DOI: 10.1016/j.neuroscience.2010.04.006

Abstract Recent findings suggest that the expression of hypothalamic–pituitary–adrenal (HPA) axis stress response adaptation in rats depends on top–down neural control. We therefore examined whether the medial prefrontal cortex (mPFC) modulates expression of stress response habituation. We transiently suppressed (muscimol microinfusion) or stimulated (picrotoxin microinfusion) mPFC neural activity in rats and studied the consequence on the first time response to psychological stress (restraint) or separately on the development and expression of habituation to repeated restraint. We monitored both the hormonal (corticosterone) and neural (forebrain c-fos mRNA) response to stress. Inactivation of the mPFC had no effect on the HPA-axis response to first time restraint, however increased mPFC activity attenuated stress-induced HPA-axis activity. In a three day repeated restraint stress regimen, inactivation of the mPFC on days 1 and 2, but not day 3, prevented the expression of HPA-axis hormone response habituation. In these same rats, the mPFC activity on day 3 interfered with the expression of c-fos mRNA habituation selectively within the mPFC, lateral septum and hypothalamic paraventricular nucleus. In contrast, inactivation of the mPFC only on day 3, or on all 3 days did not interfere with the expression of habituation. We conclude that the mPFC can permit or disrupt expression of HPA-axis stress response habituation, and this control depends on alteration of neural activity within select brain regions. A possible implication of these findings is that the dysregulation of PFC activity associated with depression and post-traumatic stress disorder may contribute to impaired expression of stress-response adaptation and consequently exacerbation of those disorders.