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Vol. 304, Issue 3, 1055-1062, March 2003
Department of Pharmacology and Experimental Therapeutics, Kyoto
Pharmaceutical University, Kyoto, Japan
We investigated the role that prostaglandins (PGs) and EP receptors
play in facilitating the gastroprotective action of capsaicin against
HCl/ethanol in rats and mice. Male Sprague-Dawley rats and
C57BL/6 mice were used after 18 h of fasting. The animals were
given HCl/ethanol (60% in 150 mM HCl) p.o. and killed 1 h later.
Capsaicin or various EP agonists were given p.o. 30 min or i.v. 10 min
before HCl/ethanol. In some cases, indomethacin or various EP agonists
were given s.c. 30 min or i.v 10 min before capsaicin, respectively.
Gastric lesions induced by HCl/ethanol were significantly inhibited by
PGE2 as well as capsaicin. The effect of PGE2
was antagonized by ONO-AE-829 (EP1 antagonist), whereas the capsaicin
action was mitigated by indomethacin as well as sensory deafferentation
but not by ONO-AE-829. The generation of mucosal PGE2 was
not affected by either capsaicin or sensory deafferentation, but was
significantly inhibited by indomethacin. Although neither butaprost
(EP2), ONO-NT-012 (EP3), nor 11-deoxy PGE1 (EP4) alone had any effect
on HCl/ethanol-induced gastric lesions, only butaprost restored the
protective action of capsaicin in the presence of indomethacin.
Capsaicin provided a protective action against HCl/ethanol-induced
gastric lesions in wild-type (+/+) mice in an indomethacin-sensitive
manner, and this action was similarly observed in EP1 (
/
) and EP3
(
/
) mice but not in the animals lacking IP receptors. These results
suggest that capsaicin exhibits gastric cytoprotection, essentially by
stimulating sensory neurons, and this action is facilitated by
endogenous PGs through EP2/IP receptors, probably sensitizing the
sensory neurons to capsaicin.
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