Abstract
Reactive oxygen species appears to be involved in the pathogenesis of ethanol-induced gastric mucosal injury in vivo. Because ingested ethanol diffuses into the gastric mucosa, targeting both epithelium and endothelium, in the present study we examined the possible protective effect of antioxidants on ethanol damage in gastric epithelial cells and endothelial cells in vitro. Cytotoxicity by ethanol was quantified by measuring 51Cr release. The effects of impairment of the glutathione redox cycle and of inhibition of cellular catalase were examined. The generation of superoxide was assessed by the reduction in cytochrome c. Ethanol caused a time- and dose-dependent increase in 51Cr release from epithelial cells. Incubation of cells withdl-buthionine-(S,R)-sulfoximine, while reducing glutathione production, dose dependently enhanced ethanol-induced injury. 1,3-Bis(chloroethyl)-nitrosourea, while inhibiting glutathione reductase activity, also sensitized cells to ethanol. In contrast, the inhibition of catalase with 3-amino-1,2,4-triazole did not alter the susceptibility of epithelial cells to ethanol. Ethanol induced damage to endothelial cells in a similar fashion. In endothelial cells, however, neither impairment of the glutathione cycle nor inhibition of catalase influenced ethanol-induced damage. Epithelial cells, when exposed to ethanol, increased superoxide production as a function of ethanol concentration, whereas endothelial cells did not. The glutathione redox cycle, but not cellular catalase, plays a critical role in protecting epithelial cells against ethanol damage, whereas neither antioxidant seems to play a role in protection of endothelial cells. The distinct difference in antioxidant protection against ethanol appears to depend on the capability of each cell to produce cytotoxic oxygen species in response to ethanol exposure.
Footnotes
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Send reprint requests to: Hideyuki Hiraishi, M.D., Second Department of Internal Medicine, Dokkyo University School of Medicine, Mibu, Tochigi 321-0293, Japan.
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↵1 This research was supported by a grant-in-aid for scientific research from the Ministry of Education, Science and Culture of Japan.
- Abbreviations:
- AT
- 3-amino-1,2,4-triazole
- BCNU
- 1,3-bis(chloroethyl)-1-nitrosourea
- BSO
- dl-buthionine-[(S,R)-sulfoximine
- DEM
- diethyl maleate
- EBSS
- Earle’s balanced salt solution
- GSH
- glutathione
- O2⨪
- superoxide anion
- ROS
- reactive oxygen species
- SOD
- superoxide dismutase
- Received April 30, 1998.
- Accepted October 28, 1998.
- The American Society for Pharmacology and Experimental Therapeutics
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