Literature DB >> 8494544

Tamoxifen inhibits lipid peroxidation in cardiac microsomes. Comparison with liver microsomes and potential relevance to the cardiovascular benefits associated with cancer prevention and treatment by tamoxifen.

H Wiseman1, M Cannon, H R Arnstein, B Halliwell.   

Abstract

Tamoxifen and 4-hydroxytamoxifen were both good inhibitors of iron-dependent lipid peroxidation in rat cardiac microsomes. Tamoxifen was also a good inhibitor of lipid peroxidation in liposomes prepared from the phospholipid obtained from rat liver microsomes. In a modified rat liver microsomal system containing a sufficiently low amount of peroxidizable phospholipid to make it comparable with the rat cardiac microsomal system, tamoxifen and 4-hydroxytamoxifen were of similar effectiveness as in the cardiac system. Tamoxifen is known to lower serum cholesterol levels, and the findings reported here indicate that the drug might also protect heart cell membranes against peroxidative damage. Potential cardioprotective and antiatherosclerotic benefits of tamoxifen are discussed in relation to the drug's use in cancer prevention and treatment.

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Year:  1993        PMID: 8494544     DOI: 10.1016/0006-2952(93)90443-z

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  3 in total

Review 1.  Review of progress in sterol oxidations: 1987-1995.

Authors:  L L Smith
Journal:  Lipids       Date:  1996-05       Impact factor: 1.880

2.  Tamoxifen reduces infiltration of inflammatory cells, apoptosis and inhibits IKK/NF-kB pathway after spinal cord injury in rats.

Authors:  Hong-Yu Wei; Xiao Ma
Journal:  Neurol Sci       Date:  2014-05-30       Impact factor: 3.307

3.  Functions of Small Organic Compounds that Mimic the HNK-1 Glycan.

Authors:  Minjuan Wang; Thomas Theis; Maciej Kabat; Gabriele Loers; Lynn A Agre; Melitta Schachner
Journal:  Int J Mol Sci       Date:  2020-09-24       Impact factor: 5.923

  3 in total

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