Literature DB >> 2343161

Gastrointestinal motor effects of corticotropin-releasing factor in mice.

R J Sheldon1, J A Qi, F Porreca, L A Fisher.   

Abstract

The present investigation examined the effects of centrally and peripherally administered corticotropin-releasing factor on gastric emptying and gastrointestinal transit in mice. Corticotropin-releasing factor, given either intracerebroventricularly or intrathecally, caused a dose-dependent inhibition of gastric emptyping and gastrointestinal transit. Intravenous or intraperitoneal administration of corticotropin-releasing factor, while 5- to 7-fold less potent than after central injection, produced an equivalent level of effect. alpha-Helical corticotropin-releasing factor, a corticotropin-releasing factor receptor antagonist, blocked the effects of intracerebroventricularly administered corticotropin-releasing factor when the antagonist was given concurrently by the intracerebroventricular, but not by the intraperitoneal, route. Conversely, corticotropin-releasing factor, when given peripherally, was antagonized equally well by intracerebroventricular or intraperitoneal administration of the antagonist. The inhibition of gastric emptying induced by corticotropin-releasing factor was reduced by pretreatment with the ganglionic blocking agent, chlorisondamine, and in adrenalectomized mice, but this effect was not antagonized by naloxone. These findings provide evidence for an action of corticotropin-releasing factor within the central nervous system, as well as a peripheral site of action, to inhibit gastric emptying in the mouse. The gastrointestinal motor effects of corticotropin-releasing factor are not mediated through opioid mechanisms although their full expression may require intact autonomic innervation and adrenal function.

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Year:  1990        PMID: 2343161     DOI: 10.1016/0167-0115(90)90013-m

Source DB:  PubMed          Journal:  Regul Pept        ISSN: 0167-0115


  10 in total

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Review 2.  Brain and Gut CRF Signaling: Biological Actions and Role in the Gastrointestinal Tract.

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Authors:  D M Barker; R Corder
Journal:  Br J Pharmacol       Date:  1999-01       Impact factor: 8.739

4.  In vivo characterization of MMP-2200, a mixed δ/μ opioid agonist, in mice.

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5.  Intracisternal urocortin inhibits vagally stimulated gastric motility in rats: role of CRF(2).

Authors:  C-Y Chen; M Million; D W Adelson; V Martínez; J Rivier; Y Taché
Journal:  Br J Pharmacol       Date:  2002-05       Impact factor: 8.739

6.  Identification of a second corticotropin-releasing factor receptor gene and characterization of a cDNA expressed in heart.

Authors:  M Perrin; C Donaldson; R Chen; A Blount; T Berggren; L Bilezikjian; P Sawchenko; W Vale
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7.  Urocortin prevents indomethacin-induced small intestinal lesions in rats through activation of CRF2 receptors.

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8.  Therapeutic potential of gastric electrical stimulation for obesity and its possible mechanisms: a preliminary canine study.

Authors:  Hui Ouyang; Jieyun Yin; J D Z Chen
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9.  Central CRF, urocortins and stress increase colonic transit via CRF1 receptors while activation of CRF2 receptors delays gastric transit in mice.

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Review 10.  Neuroendocrine control of the gut during stress: corticotropin-releasing factor signaling pathways in the spotlight.

Authors:  Andreas Stengel; Yvette Taché
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  10 in total

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