Literature DB >> 12635103

An investigation of the role of vitamin E in the protection of mice against microcystin toxicity.

Michelle M Gehringer1, Sharlene Govender, Mrinal Shah, Timothy G Downing.   

Abstract

The presence of cyanobacterial toxins in drinking and recreational waters represents a potential public health risk. Microcystin-LR (MC-LR) is a potent cyclic heptapeptide hepatotoxin produced by the blue-green alga Microcystis aeruginosa. Chemoprotectant studies have indicated that membrane-active antioxidants such as vitamin E may offer protection against microcystin toxicity. This study investigated the effect of vitamin E supplementation on microcystin toxicity in mouse liver. Groups of mice were fed vitamin E supplements (8.33 or 33.3 U/mouse/day) for 4 weeks, with intraperitoneal doses of MC-LR extract (70% LD(50)) every 3 days from day 8. The potential benefits of vitamin E were evaluated based on lipid peroxidation, alanine transaminase (ALT), and glutathione S-transferase (GST) levels. Vitamin E supplementation at 33.3 U/mouse/day offered some protection against lipid peroxidation induced by repeated exposure to MC-LR extract and limited both the toxin-induced increase in ALT leakage and decrease in GST activity. Vitamin E supplementation at 66.6 U/mouse/day significantly increased the time to death and reduced the increase in liver percentage body weight induced in mice given a lethal dose challenge of MC-LR extract. Therefore, vitamin E, taken as a dietary supplement, may have a protective effect against chronic exposure to MC-LR. Copyright 2003 Wiley Periodicals, Inc. Environ Toxicol 18: 142-148, 2003.

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Year:  2003        PMID: 12635103     DOI: 10.1002/tox.10110

Source DB:  PubMed          Journal:  Environ Toxicol        ISSN: 1520-4081            Impact factor:   4.119


  8 in total

1.  Sulforaphane prevents microcystin-LR-induced oxidative damage and apoptosis in BALB/c mice.

Authors:  Xiaoyun Sun; Lixin Mi; Jin Liu; Lirong Song; Fung-Lung Chung; Nanqin Gan
Journal:  Toxicol Appl Pharmacol       Date:  2011-05-27       Impact factor: 4.219

2.  Toxicogenomic evaluation of microcystin-LR treated with ultrasonic irradiation.

Authors:  Alice Hudder; Weihua Song; Kevin E O'Shea; Patrick J Walsh
Journal:  Toxicol Appl Pharmacol       Date:  2007-02-22       Impact factor: 4.219

3.  Sulforaphane protects Microcystin-LR-induced toxicity through activation of the Nrf2-mediated defensive response.

Authors:  Nanqin Gan; Lixin Mi; Xiaoyun Sun; Guofei Dai; Fung-Lung Chung; Lirong Song
Journal:  Toxicol Appl Pharmacol       Date:  2010-06-21       Impact factor: 4.219

Review 4.  Potential Use of Chemoprotectants against the Toxic Effects of Cyanotoxins: A Review.

Authors:  Remedios Guzmán-Guillén; María Puerto; Daniel Gutiérrez-Praena; Ana I Prieto; Silvia Pichardo; Ángeles Jos; Alexandre Campos; Vitor Vasconcelos; Ana M Cameán
Journal:  Toxins (Basel)       Date:  2017-05-23       Impact factor: 4.546

Review 5.  Microcystin Incidence in the Drinking Water of Mozambique: Challenges for Public Health Protection.

Authors:  Isidro José Tamele; Vitor Vasconcelos
Journal:  Toxins (Basel)       Date:  2020-06-02       Impact factor: 4.546

Review 6.  A Review of Cardiovascular Toxicity of Microcystins.

Authors:  Linghui Cao; Isaac Yaw Massey; Hai Feng; Fei Yang
Journal:  Toxins (Basel)       Date:  2019-08-30       Impact factor: 4.546

7.  Repeated five-day administration of L-BMAA, microcystin-LR, or as mixture, in adult C57BL/6 mice - lack of adverse cognitive effects.

Authors:  Oddvar Myhre; Dag Marcus Eide; Synne Kleiven; Hans Christian Utkilen; Tim Hofer
Journal:  Sci Rep       Date:  2018-02-02       Impact factor: 4.379

8.  Microcystins in water and in microalgae: Do microcystins as microalgae contaminants warrant the current public alarm?

Authors:  Stefano Scoglio
Journal:  Toxicol Rep       Date:  2018-08-03
  8 in total

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