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Induction to oxidative stress by saxitoxin investigated through lipid peroxidation in Neuro 2A cells and Chlamydomonas reinhardtii alga
Authors:Melegari Silvia P  Perreault François  Moukha Serge  Popovic Radovan  Creppy Edmond E  Matias William G
Institution:a Laboratory of Environmental Toxicology, LABTOX, Department of Sanitary and Environmental Engineering, Campus Universitário Trindade, CEP 88040-970 Florianopolis, SC, Brazil
b Department of Chemistry, University of Quebec in Montreal, C.P. 8888, Succ. Centre-Ville, Montreal, Quebec, Canada H3C 3P8
c Laboratory de Toxicologie et d’Hygiène Appliquée, UFR des Sciences Pharmaceutiques, Université Victor Segalen Bordeaux 2, 146 rue Léo Saignat, 33076 Bordeaux Cedex, France
d INRA, Centre de Recherche de Bordeaux Aquitaine, MICA, Unité de Mycologie et de Sécurité des Aliments, Domaine de la grande Ferrade, 71 avenue Edouart Bourleaux BP 81, 33883 Villenave d’Ornon Cedex, France
Abstract:Saxitoxin (STX) is a cyanotoxin, which can cause neurotoxic effects and induce ecological changes in aquatic environments, a potential risk to public and environmental health. Many studies of cytotoxicity on animal cells and algae have been performed, although few compare the toxic effects between the two models. In this sense, we investigated the oxidative stress induced by STX (0.4-3.0 nM) in two different cellular models: Neuro-2A (N2A) cells and Chlamydomonas reinhardtii alga by quantification of malondialdehyde (MDA) levels as indicative of lipid peroxidation (LPO). Also was evaluated the antioxidant defense of these cells systems after exposure to STX by the addition of antioxidants in N2A cells culture, and by the measure of antioxidants enzymes activity in C. reinhardtii cells. The MDA levels of N2A cells increased from 15% to 113% for 0.4 and 3.0 nM of STX, respectively, as compared to control. Superoxide-dismutase and catalase did not appear to protect the cell from STX effect while, in cells treated with vitamin E, the rates of MDA production decreased significantly, except for higher concentrations of STX. No MDA productions were observed in algal cells however some effects on antioxidant enzymes activity were observed when algae were exposed to 3.0 nM STX. Our results indicate that the concentrations of STX that may induce oxidative stress through LPO are different in animal and phytoplankton communities. A combination of algal and animal bioassays should be conducted for reliable assessment of oxidative stress induced by STX.
Keywords:STX  saxitoxin  N2A  Neuro-2A  MDA  malondialdehyde  SOD  superoxide dismutase  CAT  catalase  APX  ascorbate peroxidase  GR  glutathione reductase  GST  glutathione S-transferase  GPx  glutathione peroxidase  GSH  glutathione reduced form  RS  reactive species  ROS  reactive oxygen species  LPO  lipid peroxidation  TBA  thiobarbituric acid  HPLC  high performance liquid chromatography
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