锌对大脑脂质过氧化和金属硫蛋白水平中镉作用的影响评估。
Evaluation of zinc effect on cadmium action in lipid peroxidation and metallothionein levels in the brain.
作者信息
Braga Marcos M, Dick Tuiskon, de Oliveira Diogo L, Scopel-Guerra Adriele, Mussulini Ben Hur M, Souza Diogo O, da Rocha João Batista T
机构信息
Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, CEP 90035-003 Porto Alegre, RS, Brazil.
Departamento de Bioquímica e Biologia Molecular, Centro de Ciências Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria, RS 97105-900, Brazil.
出版信息
Toxicol Rep. 2015 Jun 5;2:858-863. doi: 10.1016/j.toxrep.2015.05.014. eCollection 2015.
Cadmium (Cd) is a known hepato- and nephrotoxic pollutant and zinc (Zn) metalloproteins are important targets of Cd. Hence, the administration of Zn may mitigate Cd toxic effects. However, the interaction of Cd and Zn has been little investigated in the brain. Previously, we reported a protective effect of Zn on mortality caused by Cd in rats. Here, we tested whether the protective effect of Zn could be related to changes in brain Zn-proteins, metallothionein (MT) and δ-aminolevulinate dehydratse (δ-ALA-D). Male adult rats were daily administered for 10 days with Zn (2 mg kg), Cd (0.25 and 1 mg kg) and 0.25 mg kg of Cd plus Zn and 1 mg kg of Cd plus Zn. The body weight loss, food intake deprivation, and mortality occurred in 1 mg kg of Cd, but Zn co-administration did mitigate these effects. The brain Zn content was not modified by treatment with Cd, whereas cerebral Cd levels increased in animals exposed to Cd. The administration of 0.25 mg kg of Cd (with or without Zn) induced lipid peroxidation and decreased MT concentration, but 2 mg kg of Zn and 1 mg kg of Cd did not change these parameters. Brain δ-ALA-D was not modified by Cd and/or Zn treatments. Since the co-administration of Zn did not attenuate the changes induced by Cd in the brain, our results suggest that the protective effect of Zn on impairments caused by Cd in animal status is weakly related to a cerebral interaction of these metals.
镉(Cd)是一种已知的具有肝毒性和肾毒性的污染物,锌(Zn)金属蛋白是镉的重要作用靶点。因此,施用锌可能会减轻镉的毒性作用。然而,镉和锌在大脑中的相互作用鲜有研究。此前,我们报道了锌对大鼠镉诱导的死亡率具有保护作用。在此,我们测试了锌的保护作用是否与脑锌蛋白、金属硫蛋白(MT)和δ-氨基乙酰丙酸脱水酶(δ-ALA-D)的变化有关。成年雄性大鼠每天分别给予锌(2毫克/千克)、镉(0.25毫克/千克和1毫克/千克)、0.25毫克/千克镉加锌以及1毫克/千克镉加锌,持续10天。体重减轻、食物摄入量减少以及死亡率在给予1毫克/千克镉的大鼠中出现,但锌的共同施用减轻了这些影响。镉处理并未改变脑锌含量,而暴露于镉的动物脑镉水平升高。给予0.25毫克/千克镉(无论是否添加锌)会诱导脂质过氧化并降低MT浓度,但2毫克/千克锌和1毫克/千克镉并未改变这些参数。镉和/或锌处理并未改变脑δ-ALA-D。由于锌的共同施用并未减弱镉在大脑中诱导的变化,我们的结果表明,锌对动物状态下镉所致损伤的保护作用与这些金属在大脑中的相互作用关系较弱。