首页> 外文期刊>Toxicology mechanisms and methods >Induction of genotoxicity and differential alterations of p53 and inflammatory cytokines expression by acute oral exposure to bulk- or nano-calcium hydroxide particles in mice 'Genotoxicity of normal- and nano-calcium hydroxide'
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Induction of genotoxicity and differential alterations of p53 and inflammatory cytokines expression by acute oral exposure to bulk- or nano-calcium hydroxide particles in mice 'Genotoxicity of normal- and nano-calcium hydroxide'

机译:急性口腔暴露于小鼠“正常与纳米氢氧化钙的遗传毒性”,急性口腔暴露于急性口腔暴露于致氧化物或纳米钙氧化物颗粒的遗传毒性和炎症细胞因子表达的诱导

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摘要

With the high increases in the uses of calcium hydroxide in various applications due its distinctive properties, human exposure has increased to normal- and nano-calcium hydroxide. However, its impact on the DNA integrity, expression of inflammatory cytokines, and induction of oxidative stress has not been clearly studied. Therefore, here we estimate the induction of DNA damage, inflammation, and oxidative stress in mice orally administrated a single dose (100 mg/kg) of normal- or nano-sized calcium hydroxide for 24 hour. Comet, Diphenylamine and laddered DNA fragmentation assays were done to assess DNA damage induction. Acute oral administration of normal- or nano-calcium hydroxide particles disrupted the DNA integrity, caused generation of ROS and also concurrent increases in both the nitric oxide concentration and inducible nitric oxide synthase gene expression in a reverse proportional to the calcium hydroxide particles' size. Increases in the concentration of calcium ions as well as alterations in the expression level of p53 and proinflammatory cytokines were also observed in calcium hydroxide administrated groups. Moreover, administration of normal- or nano-calcium hydroxide particles suspension elevated the level of malondialdehyde and decreased both the glutathione peroxidase activity and the reduced glutathione level, as well as caused tissue injuries (e.g. renal tube degeneration, congested blood vessels, atrophied lymphoid follicles, interstitial inflammatory reaction, and hyalinosis of myocardial muscles). Thus, we conclude that calcium hydroxide acutely orally administrated in its ordinary or nano-particulate form causes DNA damage induction by generating free radicals and altering the expression levels of p53 gene and proinflammatory cytokines.
机译:由于氢氧化钙的独特性质,其在各种应用中的使用量大幅增加,人类接触到的普通和纳米氢氧化钙也增加了。然而,其对DNA完整性、炎性细胞因子表达和氧化应激诱导的影响尚未得到明确研究。因此,在这里,我们评估了单剂量(100 mg/kg)正常或纳米级氢氧化钙24小时口服给药的小鼠对DNA损伤、炎症和氧化应激的诱导作用。彗星试验、二苯胺试验和梯状DNA断裂试验用于评估DNA损伤诱导。急性口服正常或纳米氢氧化钙颗粒会破坏DNA完整性,导致活性氧的产生,同时一氧化氮浓度和诱导型一氧化氮合酶基因表达也会增加,与氢氧化钙颗粒的大小成反比。氢氧化钙给药组的钙离子浓度增加,p53和促炎细胞因子的表达水平也发生改变。此外,服用正常或纳米氢氧化钙颗粒悬浮液会提高丙二醛水平,降低谷胱甘肽过氧化物酶活性和还原型谷胱甘肽水平,以及引起的组织损伤(如肾小管变性、血管充血、淋巴滤泡萎缩、间质炎症反应和心肌透明质增生)。因此,我们得出结论,以普通或纳米颗粒形式急性口服氢氧化钙,通过产生自由基和改变p53基因和促炎细胞因子的表达水平,导致DNA损伤诱导。

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