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Dissecting adrenal and behavioral responses to stress by targeted gene inactivation in mice

  • Judson A. Brewer
  • , Kathleen E. Bethin
  • , Michele L. Schaefer
  • , Lisa M. Muglia
  • , Sherri K. Vogt
  • , Stacie C. Weninger
  • , Joseph A. Majzoub
  • , Louis J. Muglia
  • Washington University St. Louis
  • Boston Children's Hospital

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

To define the molecular pathways modulating adrenal and behavioral responses to stress, we have generated mice with inactivation of hypothalamic neuropeptides and signaling pathways. Studies in mice deficient in corticotropin-releasing hormone (CRH) have revealed the essential role for CRH in adrenal glucocorticoid production in response to many physiological and psychological stressors. Immune system activation in CRH-deficient mice provides a unique exception to the necessity for CRH in stimulating adrenal glucocorticoid production. By analyzing mice deficient in interleukin-6 (IL-6) and CRH, we find that restoration of glucocorticoid output with inflammation is largely mediated by dysregulated IL-6 production. Current studies focus on identifying cellular and gene targets by which glucocorticoids regulate immune system function. In contrast to impaired adrenocortical responses to stress, CRH-deficient mice exhibit normal behavioral responses to stress. To determine signaling pathways that may contribute to the behavioral responses to stress, we have generated and analyzed mice deficient in adenylyl cyclase type 8 (AC8). AC8 deficient mice have intact adrenocortical responses to stress, but an inability to undergo stress-induced alterations in behavior.

Original languageEnglish
Pages (from-to)121-125
Number of pages5
JournalStress
Volume6
Issue number2
DOIs
StatePublished - Jun 2003

Keywords

  • Adenylyl cyclase
  • Anxiety
  • Corticotropin-releasing hormone
  • Glucocorticoid receptor
  • Green fluorescent protein
  • Interleukin-6

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