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Limbic corticotropin-releasing hormone receptor 1 mediates anxiety-related behavior and hormonal adaptation to stress.

Corticotropin-releasing hormone (CRH) is centrally involved in coordinating responses to a variety of stress-associated stimuli. Recent clinical data implicate CRH in the pathophysiology of human affective disorders. To differentiate the CNS pathways involving CRH and CRH receptor 1 (Crhr1) that modulate behavior from those that regulate neuroendocrine function, we generated a conditional knockout mouse line (Crhr1(loxP/loxP)Camk2a-cre) in which Crhr1 function is inactivated postnatally in anterior forebrain and limbic brain structures, but not in the pituitary. This leaves the hypothalamic-pituitary-adrenocortical (HPA) system intact. Crhr1(loxP/loxP)Camk2a-cre mutants showed reduced anxiety, and the basal activity of their HPA system was normal. In contrast to Crhr1 null mutants, conditional mutants were hypersensitive to stress corticotropin and corticosterone levels remained significantly elevated after stress. Our data clearly show that limbic Crhr1 modulates anxiety-related behavior and that this effect is independent of HPA system function. Furthermore, we provide evidence for a new role of limbic Crhr1 in neuroendocrine adaptation to stress.

Pubmed ID: 12973355

Authors

  • Müller MB
  • Zimmermann S
  • Sillaber I
  • Hagemeyer TP
  • Deussing JM
  • Timpl P
  • Kormann MS
  • Droste SK
  • Kühn R
  • Reul JM
  • Holsboer F
  • Wurst W

Journal

Nature neuroscience

Publication Data

October 26, 2003

Associated Grants

None

Mesh Terms

  • Adaptation, Physiological
  • Animals
  • Anxiety Disorders
  • Behavior, Animal
  • Corticotropin-Releasing Hormone
  • Hypothalamo-Hypophyseal System
  • Limbic System
  • Male
  • Mice
  • Mice, Knockout
  • Mutation
  • Neural Pathways
  • Pituitary-Adrenal System
  • Prosencephalon
  • RNA, Messenger
  • Receptors, Corticotropin-Releasing Hormone
  • Receptors, Mineralocorticoid
  • Stress, Physiological