Acute stress causes mucin release from rat colon: role of corticotropin releasing factor and mast cells

Ignazio Castagliuolo(Beth Israel Deaconess Hospital), J. Thomas LaMont(Beth Israel Deaconess Hospital), Bosheng Qiu(Beth Israel Deaconess Hospital), Sheila M. Fleming(Beth Israel Deaconess Hospital), K. Ramakrishnan Bhaskar(Beth Israel Deaconess Hospital), Sigfús Nikulásson(Beth Israel Deaconess Hospital), Conan Kornetsky(Beth Israel Deaconess Hospital), Charalabos Pothoulakis(Beth Israel Deaconess Hospital)
American Journal of Physiology-Gastrointestinal and Liver Physiology
November 1, 1996
Cited by 249

Abstract

We determined the effects of immobilization stress on rat colonic mucus release and mast cell degranulation and examined whether corticotropin releasing factor (CRF) was involved in these responses. After 30-min immobilization, rats were killed, colonic mucosal explants were cultured, and levels of rat mast cell protease II (RMCP II) and prostaglandin E2 (PGE2) were measured. Mucin release from explants was assayed by incorporation of [3H]glucosamine into colonic mucin and by histological evaluation of goblet cell depletion. Stress caused significant increases of colonic RMCP II, PGE2, and mucin release and fecal pellet output and caused an approximately 10-fold increase in colonic mucosal levels of cyclooxygenase-2 (COX-2) mRNA. These stress-associated changes were reproduced by intravenous or intracerebral injection of CRF in conscious, nonstressed rats. Pretreatment of rats with the CRF antagonist alpha-helical-CRF9-41, hexamethonium, atropine, or bretylium, or the mast cell stabilizer lodoxamide inhibited stress-induced release of RMCP II, PGE2, and mucin, whereas indomethacin prevented mucin release but not mast cell degranulation. Hexamethonium and CP-96,345, a substance P antagonist, inhibited fecal pellet output caused by stress. We conclude that CRF released during immobilization stress increases colonic transit via a neuronal pathway and stimulates colonic mucin secretion via activation of neurons and mast cells.


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