Peer-Reviewed Journal Details
Mandatory Fields
Carroll, SY,O'Mahony, SM,Grenham, S,Cryan, JF,Hyland, NP
2013
December
Plos One
Disodium Cromoglycate Reverses Colonic Visceral Hypersensitivity and Influences Colonic Ion Transport in a Stress-Sensitive Rat Strain
Published
Optional Fields
IRRITABLE-BOWEL-SYNDROME PERITONEAL MAST-CELLS NEONATAL MATERNAL-DEPRIVATION INDUCED HISTAMINE-RELEASE CONNECTIVE-TISSUE-TYPE LONG-TERM ALTERATIONS SODIUM CROMOGLYCATE ANTIALLERGIC COMPOUNDS RESTRAINT STRESS IN-VITRO
8
The interface between psychiatry and stress-related gastrointestinal disorders (GI), such as irritable bowel syndrome (IBS), is well established, with anxiety and depression the most frequently occurring comorbid conditions. Moreover, stress-sensitive Wistar Kyoto (WKY) rats, which display anxiety-and depressive-like behaviors, exhibit GI disturbances akin to those observed in stress-related GI disorders. Additionally, there is mounting preclinical and clinical evidence implicating mast cells as significant contributors to the development of abdominal visceral pain in IBS. In this study we examined the effects of the rat connective tissue mast cell (CTMC) stabiliser, disodium cromoglycate (DSCG) on visceral hypersensitivity and colonic ion transport, and examined both colonic and peritoneal mast cells from stress-sensitive WKY rats. DSCG significantly decreased abdominal pain behaviors induced by colorectal distension in WKY animals independent of a reduction in colonic rat mast cell mediator release. We further demonstrated that mast cell-stimulated colonic ion transport was sensitive to inhibition by the mast cell stabiliser DSCG, an effect only observed in stress-sensitive rats. Moreover, CTMC-like mast cells were significantly increased in the colonic submucosa of WKY animals, and we observed a significant increase in the proportion of intermediate, or immature, peritoneal mast cells relative to control animals. Collectively our data further support a role for mast cells in the pathogenesis of stress-related GI disorders.
10.1371/journal.pone.0084718
Grant Details