Lipocortin-1 inhibits CRH stimulation of plasma ACTH and IL-1 beta-stimulated hypothalamic CRH release in rats.

A Sudlow, F Carey, R Forder, NJ. Rothwell

Research output: Contribution to journalArticlepeer-review

Abstract

A 188-amino acid NH2-terminal fragment of recombinant human lipocortin-1 (rhLC-1) (LC-1 fragment) mimics glucocorticoid (and rhLC-1) inhibition of corticotrophin-releasing hormone (CRH)-stimulated release of adrenocorticotrophin (ACTH) from rat anterior pituitary and cytokine-stimulated CRH release from rat hypothalamus in vitro. The present in vivo study examined the effect of LC-1 fragment on CRH stimulation of rat plasma ACTH and release of rat hypothalamic CRH. Coinjection of LC-1 fragment inhibited the increase in plasma ACTH concentration stimulated by either central (76% inhibition) or peripheral (72% inhibition) injection of CRH and abolished the (62%) depletion of hypothalamic immunoreactive (ir)CRH stimulated by central injection of interleukin-1 beta. Central injection of the CRH functional analogue sauvagine led to a 46% reduction (P > 0.05, 2-way analysis of variance) in rat hypothalamic irCRH content, which was reversed by coinjection of LC-1 fragment. These results indicate that LC-1 can suppress the activity of the hypothalamic-pituitary axis in the rat, possibly by inhibiting a positive feedback mechanism controlling release of hypothalamic CRH.
Original languageEnglish
JournalAm J Physiol
Volume270( 1 Pt 2)
Publication statusPublished - Jan 1996

Keywords

  • Animals
  • pharmacology: Annexin I
  • blood: Corticotropin
  • antagonists & inhibitors: Corticotropin-Releasing Hormone
  • Human
  • metabolism: Hypothalamus
  • Immunoradiometric Assay
  • pharmacology: Interleukin-1
  • Male
  • Osmolar Concentration
  • pharmacology: Peptide Fragments
  • pharmacology: Peptides
  • Radioimmunoassay
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins
  • Support, Non-U.S. Gov't

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