Literature DB >> 9164262

Dietary modulation of oxidative stress in alcoholic liver disease in rats.

E A Porta1.   

Abstract

Numerous studies dealing with prolonged feeding of rats with ethanol liquid regimens high in fat and low in carbohydrate showed that the resulting hepatic pathologic changes, including increased lipid peroxidation, are due to dietary aberrations rather than to ethanol toxicity. The amount and particularly the type of dietary fat significantly modulate the hepatic oxidative stress and morphofunctional reactivities. Although dietary vitamin E modulated oxidative stress or lipid peroxidation, it did not influence the development of hepatic pathologic changes in different animal models of chronic alcoholism. The old observation that lipotropes modulate the hepatic alterations associated with prolonged excessive ingestion of ethanol has been amply confirmed by even those who for years did not accept the importance of lipotropes. Our recent studies in rats indicated that prolonged feeding of large amounts of ethanol and diets with variable amounts of lipotropes, vitamin E and minerals did not significantly modulate a large series of hepatic prooxidants, but decreased several antioxidants (vitamin E, ubiquinols and glutathione peroxidase). Ethanol regimens relatively low in vitamin E increased the hepatic thiobarbituric acid-reactive substances and chemiluminescence and reduced some of the antioxidant factors. However, the hepatic prooxidant factors were unaffected, and no liver damage was detected. These and other findings indicated that the eventual detection of oxidative stress in experimental alcoholic liver disease primarily depends on the type of diet and that oxidative stress may not play a significant pathogenic role in this condition.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9164262     DOI: 10.1093/jn/127.5.912S

Source DB:  PubMed          Journal:  J Nutr        ISSN: 0022-3166            Impact factor:   4.798


  5 in total

1.  Gestational Iron Supplementation Improves Fetal Outcomes in a Rat Model of Prenatal Alcohol Exposure.

Authors:  Kaylee K Helfrich; Nipun Saini; Sze Ting Cecilia Kwan; Olivia C Rivera; Rachel Hodges; Susan M Smith
Journal:  Nutrients       Date:  2022-04-15       Impact factor: 6.706

2.  Monascin and Ankaflavin of Monascus purpureus Prevent Alcoholic Liver Disease through Regulating AMPK-Mediated Lipid Metabolism and Enhancing Both Anti-Inflammatory and Anti-Oxidative Systems.

Authors:  Jhao-Ru Lai; Ya-Wen Hsu; Tzu-Ming Pan; Chun-Lin Lee
Journal:  Molecules       Date:  2021-10-18       Impact factor: 4.411

3.  Effects of vitamin C and E supplementation on oxidative stress and liver toxicity in rats fed a low-fat ethanol diet.

Authors:  Soo-Jung Lee; Seon-Young Kim; Hyesun Min
Journal:  Nutr Res Pract       Date:  2013-04-01       Impact factor: 1.926

4.  PROUD: effects of preoperative long-term immunonutrition in patients listed for liver transplantation.

Authors:  Arash Nickkholgh; Heinz Schneider; Jens Encke; Markus W Büchler; Jan Schmidt; Peter Schemmer
Journal:  Trials       Date:  2007-08-27       Impact factor: 2.279

Review 5.  Beneficial effects of naringenin in liver diseases: Molecular mechanisms.

Authors:  Erika Hernández-Aquino; Pablo Muriel
Journal:  World J Gastroenterol       Date:  2018-04-28       Impact factor: 5.742

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.