Abstract | OBJECTIVE: Oxidative stress plays a central role in the initiation and progression of liver disease. Chronic ethanol consumption induces oxidative damage of the liver. Using a rat model, we previously showed that chronic administration of lipopolysaccharide and proteases to gingival sulcus induced both periodontal inflammation and liver injury. Periodontitis and ethanol consumption may have an additional effect on hepatic oxidative damage. The present study investigated the effects of periodontitis on ethanol-induced oxidative damage of the liver using a rat model. DESIGN: Male Wistar rats were divided into four groups (six rats/group). During the experimental period of eight weeks, two groups were fed an ethanol-containing liquid diet, and two groups were on a pair-fed control diet. Four weeks prior to the end of the experimental period, one group from each dietary treatment was ligated to induce periodontitis, while the other group was left unligated. In order to evaluate hepatic oxidative damage, the level of hexanoyl- lysine and the ratio of reduced form glutathione/oxidized form glutathione (GSH/ GSSG) was determined. The concentration of blood hexanoyl- lysine was also measured as an index of circulating lipid peroxide. RESULTS: CONCLUSION:
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Authors | Takaaki Tomofuji, Toshihiro Sanbe, Daisuke Ekuni, Tetsuji Azuma, Koichiro Irie, Takayuki Maruyama, Naofumi Tamaki, Tatsuo Yamamoto |
Journal | Archives of oral biology
(Arch Oral Biol)
Vol. 53
Issue 12
Pg. 1113-8
(Dec 2008)
ISSN: 1879-1506 [Electronic] England |
PMID | 18603227
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Animals
- Ethanol
(metabolism, pharmacology)
- Ligation
- Lipid Peroxidation
(drug effects)
- Liver
(drug effects, metabolism)
- Liver Diseases, Alcoholic
(metabolism)
- Male
- Oxidative Stress
(drug effects)
- Periodontitis
(etiology, metabolism)
- Rats
- Rats, Wistar
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