1. Evaluation of genotoxicity and antigenotoxicity of astaxanthin by the Comet assay in mammalian cells in vitro 2013
- Author
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Ferreira, Micheli de Moraes, Abrantes, Shirley de Mello Pereira, Zamith, Helena Pereira da Silva, Azevedo-Meleiro, Cristiane Hess de, and Silva, Marco Antonio Mota da
- Subjects
Genotoxicidade ,Ci?ncia e Tecnologia de Alimentos ,Ensaio cometa ,Caroten?ides ,Genotoxicity ,Comet assays ,Carotenoids - Abstract
Submitted by Leticia Schettini (leticia@ufrrj.br) on 2022-03-14T14:21:46Z No. of bitstreams: 1 2013 - Micheli de Moraes Ferreira.pdf: 1455175 bytes, checksum: 5c2f286e2f1aada2fb86e881eab57e01 (MD5) Made available in DSpace on 2022-03-14T14:21:47Z (GMT). No. of bitstreams: 1 2013 - Micheli de Moraes Ferreira.pdf: 1455175 bytes, checksum: 5c2f286e2f1aada2fb86e881eab57e01 (MD5) Previous issue date: 2013-07-30 CAPES The color and appearance of food are the first fundamental attributes, if not more important, to be evaluated by consumers at the time of its acquisition. The food can be more nutritious, safer and more economical, however, if not attractive, its acquisition will not occur. The salmon is basically a white fish that becomes pink by eating shrimp. The stored red pigment present in muscle or shrimp in the shell and accumulates in adipose tissue is acquired through ingestion algae and unicellular organisms by the shrimps from the sea. Carotenoids used in food, pharmaceutical, cosmetics and food are natural colorants responsible for yellow, orange and red. The raised salmon aquaculture has no access to the bodies mentioned above, however, it is added to their feed astaxanthin (ATX), a substance that gives a pinkish color to your meat. ATX (3,3 '-dihydroxy-beta, beta-carotene-4, 4'-dione) is a oxygenated carotenoid pigment that confers the characteristic reddish-pink coloration of certain fish, crustaceans, birds and microorganisms. The ATX has potent activity in scavenging free radicals and protecting against lipid peroxidation and the damage caused by oxidation of cell membranes and tissues. In this study we investigated in human blood cells in vitro genotoxicity and protective effect or antigenotoxicity ATX induction of oxidative DNA damage caused by hydrogen peroxide (H2O2). ATX (0.1 to 5 ?M) was not cytotoxic in human blood cells are cytotoxic in the range 10-1000 ?M inducing 1 to 10% mortality when compared to control cell-solvent dimethylsulfoxide (DMSO 5%). The ATX Comet assays performed did not induce DNA damage (p> 0.1) on human blood cells tested in the range 0.1 to 500 ?M compared to the 5% DMSO. H2O2 (12.5 to 2000 ?M) was not cytotoxic and did not cause cell lethality in human blood cells but was genotoxic (p 0,1) em c?lulas sangu?neas humanas na faixa testada de 0,1 a 500 ?M quando comparado ao DMSO 5%.. O H2O2 (12,5 a 2000 ?M) n?o foi citot?xico n?o causando letalidade celular em c?lulas sangu?neas humanas, por?m foi genot?xico (p
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- 2013