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Divisions of 1 Gastroenterology
and 2 Experimental Pathology,
We recently reported that immobilization
stress increased colonic motility, mucin, and prostaglandin
E2
(PGE2) release and mucosal mast
cell degranulation in rat colon [Proc. Natl.
Acad. Sci. USA 93: 12611-12615, 1996;
Am. J. Physiol. 271 (Gastrointest. Liver Physiol. 34):
G884-G892, 1996]. To directly assess the contribution of
mast cells, we compared colonic responses to stress in mast cell-deficient
KitW/KitW
v
and normal (+/+) mice. Mucin and
PGE2 release were measured in colonic explants cultured from
KitW/KitW
v
and (+/+) mice 30 min after immobilization stress. We found that stress
stimulated colonic mucin release (1.8-fold), goblet cell depletion
(3-fold), and PGE2 (2.3-fold)
release in (+/+) but not mast cell-deficient
KitW/KitW
v
mice. However, mast cell-deficient mice that had their mast cell population reconstituted by injection of bone marrow-derived mast cells
from (+/+) mice had colonic responses to stress similar to those of
normal (+/+) mice. In contrast, colonic transit changes in response to
stress, estimated by fecal output, were similar between
KitW/KitW
v
and normal (+/+) mice. We conclude that mast cells regulate colonic mucin and PGE2 release but not
colonic transit changes in response to immobilization stress.
mast cell-deficient mice; prostaglandin E2; colonic motility; hypothalamic-pituitary-adrenal axis; central nervous system
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