Selenium and mercury levels in rat liver slices co-treated with diphenyl diselenide and methylmercury

被引:12
作者
Dalla Corte, Cristiane Lenz [1 ,3 ,4 ]
Ramos, Angelica [1 ]
Moreira dos Santos, Clarissa Marques [2 ]
Dressler, Valderi Luiz [2 ]
Teixeira da Rocha, Joao Batista [1 ,4 ]
机构
[1] Univ Fed Santa Maria, Ctr Ciencias Nat & Exatas, Programa Posgrad Ciencias Biol Bioquim Toxicol, Dept Bioquim & Biol Mol, BR-97105900 Santa Maria, RS, Brazil
[2] Univ Fed Santa Maria, LAQIA, BR-97105900 Santa Maria, RS, Brazil
[3] Univ Fed Pampa, Campus Cacapava Sul,Av Pedro Anunciacao 111, BR-96570000 Cacapava Do Sul, RS, Brazil
[4] Univ Fed Santa Maria, CCNE, Dep Bioquim & Biol Mol, BR-97105900 Santa Maria, RS, Brazil
关键词
Methylmercury; Selenium; ICP-MS; Mitochondria; Liver slices; MITOCHONDRIAL DYSFUNCTION; OXIDATIVE STRESS; GLUTAMATE UPTAKE; CORTICAL SLICES; ADULT MICE; TOXICITY; EBSELEN; BRAIN; CNS;
D O I
10.1007/s10534-016-9936-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Organoseleno-compounds have been investigated for its beneficial effects against methylmercury toxicity. In this way, diphenyl diselenide (PhSe)(2) was demonstrated to decrease Hg accumulation in mice, protect against MeHg-induced mitochondrial dysfunction, and protect against the overall toxicity of this metal. In the present study we aimed to investigate if co-treatment with (PhSe)(2) and MeHg could decrease accumulation of Hg in liver slices of rats. Rat liver slices were co-treated with (PhSe)(2) (0.5; 5 A mu M) and/or MeHg (25 A mu M) for 30 min at 37 A degrees C and Se and Hg levels were measured by inductively coupled plasma mass spectrometry (ICP-MS) in the slices homogenate, P1 fraction, mitochondria and incubation medium. Co-treatment with (PhSe)(2) and MeHg did not significantly alter Se levels in any of the samples when compared with compounds alone. In addition, co-treatment with (PhSe)(2) and MeHg did not decrease Hg levels in any of the samples tested, although, co-incubation significantly increased Hg levels in homogenate. We suggest here that (PhSe)(2) could exert its previously demonstrated protective effects not by reducing MeHg levels, but forming a complex with MeHg avoiding it to bind to critical molecules in cell.
引用
收藏
页码:543 / 550
页数:8
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