{"title":"Protective/detoxicative function of metallothionein in the rat brain and blood induced by controlled cadmium doses","authors":"H. Shiyntum, G. A. Ushakovа","doi":"10.15421/021519","DOIUrl":null,"url":null,"abstract":"Cadmium classified as a major carcinogen is considered a poisonous and unwanted heavy metal to a lot of tissues in many organism s . Of many publications already available , the general consensus is that the cadmium attenuating element is metallothionein (MT) through its interchangeable mechanism with Zn triggered by the presence of Cd, providing binding sites for Cd ions. MT was first discovered in the kidney cortex of the horse ; it represents a low molecular weight protein, rich in cysteine residues which effectively bind with metals. It s functions consist in detoxification of heavy metals like mercury, arseni c, cadmium, homeostasis of essential metals including copper and zinc, anti-oxidation against reactive oxygen species, protection against DNA damage, oxidative stress, cell survival, angiogenesis, apoptosis, and increase of proliferation. In this work, we sought to highlight the protective function of MT in the brain and serum of rats by means of detoxification under induced effects of controlled Cd doses. We have done this by exposing Wistar rats to Cd at different doses in drinking water at different time intervals. In two independent experiments , 58 rats were subjected to 0.1 or 1.0 µg Cd 2+ /kg of body weight for 15 or 36 days under different conditions. The obtained data indicates the different functioning systems for the brain and the blood for MT metabolism under Cd effect. Our results indicate significant loss of metallothionein level in the brain and important increases in the amount of MT in serum proving that even minimal ingestion of toxic Cd is enough to trigger the release of MT protein in blood.","PeriodicalId":345307,"journal":{"name":"Visnyk of Dnipropetrovsk University. Biology, medicine","volume":"5 3 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2015-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Visnyk of Dnipropetrovsk University. Biology, medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15421/021519","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
Cadmium classified as a major carcinogen is considered a poisonous and unwanted heavy metal to a lot of tissues in many organism s . Of many publications already available , the general consensus is that the cadmium attenuating element is metallothionein (MT) through its interchangeable mechanism with Zn triggered by the presence of Cd, providing binding sites for Cd ions. MT was first discovered in the kidney cortex of the horse ; it represents a low molecular weight protein, rich in cysteine residues which effectively bind with metals. It s functions consist in detoxification of heavy metals like mercury, arseni c, cadmium, homeostasis of essential metals including copper and zinc, anti-oxidation against reactive oxygen species, protection against DNA damage, oxidative stress, cell survival, angiogenesis, apoptosis, and increase of proliferation. In this work, we sought to highlight the protective function of MT in the brain and serum of rats by means of detoxification under induced effects of controlled Cd doses. We have done this by exposing Wistar rats to Cd at different doses in drinking water at different time intervals. In two independent experiments , 58 rats were subjected to 0.1 or 1.0 µg Cd 2+ /kg of body weight for 15 or 36 days under different conditions. The obtained data indicates the different functioning systems for the brain and the blood for MT metabolism under Cd effect. Our results indicate significant loss of metallothionein level in the brain and important increases in the amount of MT in serum proving that even minimal ingestion of toxic Cd is enough to trigger the release of MT protein in blood.
镉被列为主要致癌物,被认为是一种有毒的重金属,对许多生物体的许多组织都有害。在现有的许多出版物中,普遍的共识是,镉衰减元素是金属硫蛋白(MT),通过其与镉存在引发的锌的可互换机制,为镉离子提供结合位点。MT最早发现于马的肾皮质;它是一种低分子量的蛋白质,富含半胱氨酸残基,能有效地与金属结合。它的功能包括对汞、砷、镉等重金属的解毒,对铜和锌等必需金属的体内平衡,对活性氧的抗氧化,对DNA损伤的保护,氧化应激,细胞存活,血管生成,细胞凋亡和增殖的增加。在这项工作中,我们试图通过控制Cd剂量诱导下的解毒来突出MT在大鼠大脑和血清中的保护功能。我们让Wistar大鼠在不同时间间隔的饮用水中接触不同剂量的镉。在两个独立的实验中,58只大鼠在不同条件下接受0.1或1.0µg Cd 2+ /kg体重15或36天。所获得的数据表明,在Cd效应下,脑和血液对MT代谢的功能系统不同。我们的研究结果表明,大脑中金属硫蛋白水平显著下降,血清中MT含量显著增加,这证明即使微量摄入有毒Cd也足以触发血液中MT蛋白的释放。