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Effects of N-Acetylcysteine, Quercetin, and Phytic Acid on Spontaneous Hepatic and Renal Lesions in LEC Rats
1 Division of Pathology, National Institute of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan Correspondence: Address correspondence to: Akiyoshi Nishikawa, Division of Pathology, National Institute of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan; e-mail:nishikaw{at}nihs.go.jp The effects of anti-oxidants were examined in Long-Evans Cinnamon (LEC) rats, which develop acute hepatic injury, and subsequent hepatic and renal tumors due to accumulation of excess Cu. The rats, at the age of 15 weeks, were supplied a diet containing either 1% of N-acetylcysteine (NAC), quercetin (QC), or phytic acid (PA), or basal diet alone. At weeks 2 and 6 posttreatment, animals were sacrificed for collection of blood and tissue samples. In the NAC-treated group, the development of hepatic and renal lesions was dramatically reduced. In addition, accumulation of Cu and Fe in the liver was suppressed. Acrolein-modified protein, a new marker for lipid peroxidation, was not detected in the liver or kidney of NAC treated rats, even though deposition was evident in control. Neither QC nor PA affected the development of spontaneous hepatic lesions. These results indicate that oxidative stress was reduced by NAC in the liver and kidney, and suggest that Cu and Fe may be involved in the generation of oxidative stress in the liver. In addition, it was suggested that the different effects of the anti-oxidants on lesion development in LEC rats might be related to different mechanisms of action with regard to oxidative stress.
Key Words: Anti-oxidants N-acetylcysteine quercetin phytic acid LEC rat acrolein-modified protein oxidative stress: glutathione Abbreviations: LEC, Long–Evans Cinnamon NAC, N-acetylcysteine QC, quercetin PA, phytic acid ROS, reactive oxygen species 8-OHdG, 8-hydroxydeoxyguanosine GSH, glutathione TP, total protein A/G, albumin/globulin ratio AlB, albumin T.Cho, total cholesterol BUN, blood urea nitrogen CRN, creatinine Ca, calcium P, inorganic phosphate Fe, iron TIBC, total iron binding capacity UIBC, unsaturated iron binding capacity Cu, copper AST, aspartate aminotransferase ALT, alanine amino-transferase LDH, lactate dehydrogenase AlP, alkaline phosphatase
Toxicologic Pathology, Vol. 33, No. 5,
584-592 (2005) |
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