Literature DB >> 8005528

Protection by vitamin E selenium, trolox C, ascorbic acid palmitate, acetylcysteine, coenzyme Q, beta-carotene, canthaxanthin, and (+)-catechin against oxidative damage to liver slices measured by oxidized heme proteins.

H Chen1, A L Tappel.   

Abstract

Male SD rats were fed a vitamin E- and selenium-deficient diet, a diet supplemented with vitamin E and selenium, and diets supplemented with vitamin E, selenium, trolox C, ascorbic acid palmitate, acetylcysteine, beta-carotene, canthaxanthin, coenzyme Q0, coenzyme Q10, and (+)-catechin. Liver slices were incubated at 37 degrees C with and without CBrCl3, t-butyl-hydroperoxide, Fe+2, or Cu+2. The effect of antioxidant nutrients on the oxidative damage to rat liver was studied by measurement of the production of oxidized heme proteins (OHP) during the oxidative reactions. Diet supplemented with vitamin E and selenium showed a strong protection against heme protein oxidation compared to the antioxidant-deficient diet. Furthermore, increasing the diversity and quantity of antioxidants in the diets provided significantly more protection.

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Year:  1994        PMID: 8005528     DOI: 10.1016/0891-5849(94)90120-1

Source DB:  PubMed          Journal:  Free Radic Biol Med        ISSN: 0891-5849            Impact factor:   7.376


  4 in total

1.  Reduction in hypericin-induced phototoxicity by Hypericum perforatum extracts and pure compounds.

Authors:  Laura A Schmitt; Yi Liu; Patricia A Murphy; Jacob W Petrich; Philip M Dixon; Diane F Birt
Journal:  J Photochem Photobiol B       Date:  2006-07-21       Impact factor: 6.252

2.  Protection by multiple antioxidants against lipid peroxidation in rat liver homogenate.

Authors:  H Chen; A Tappel
Journal:  Lipids       Date:  1996-01       Impact factor: 1.880

Review 3.  The role of ascorbate in antioxidant protection of biomembranes: interaction with vitamin E and coenzyme Q.

Authors:  R E Beyer
Journal:  J Bioenerg Biomembr       Date:  1994-08       Impact factor: 2.945

Review 4.  Inhibition of GTRAP3-18 may increase neuroprotective glutathione (GSH) synthesis.

Authors:  Koji Aoyama; Toshio Nakaki
Journal:  Int J Mol Sci       Date:  2012-09-20       Impact factor: 6.208

  4 in total

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