H. Sakai et al., Cyclic GMP-dependent cytoprotection against ethanol-induced damage in rabbit isolated gastric parietal cells, EUR J PHARM, 361(1), 1998, pp. 109-117
Prostaglandin E-2 stimulates a nitric oxide/cyclic GMP (NO/cGMP) pathway wh
ich activates basolateral Cl- channels in rabbit gastric parietal cells. We
examined whether the NO/cGMP pathway protects parietal cells from ethanol
(EtOH)-induced cytotoxicity, using a parietal cell-rich suspension purified
from rabbit gastric mucosa. Cytotoxicity was assayed by measuring the rele
ase of a fluorescent dye from the cells. N-2,O-2-dibutyryl guanosine 3',5'-
cyclic monophosphate (DBcGMP) showed a concentration-dependent protective e
ffect against EtOH-induced cytotoxicity. The half-maximal effect of DBcGMP
was observed at 24 mu M. DBcCMP in a concentration-dependent manner opened
the basolateral Cl- channels of parietal cells, the EC50 value being 44 mu
M. The EtOH-induced cytotoxicity decreased as the Cl- concentration of medi
um decreased. A 30-s treatment with 5-nitro-2-(3-phenylpropylamino)-benzoat
e (NPPB), an inhibitor of the Cl- channel, had a cytotoxic effect which was
not prevented by pre-incubation with DBcGMP. The cytotoxic effects of EtOH
and NPPB were additive and the NPPB effects did not depend on the medium C
l- concentration. The present study showed that cGMP protects the gastric p
arietal cell from EtOH-induced cytotoxicity, and this cytoprotection is rel
ated to basolateral Cl- channel activity in the plasma membrane via an unkn
own mechanism(s). (C) 1998 Elsevier Science B.V. All rights reserved.