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Effects of vitamin A and vitamin E on attenuation of titanium dioxide nanoparticles-induced toxicity in the liver of male Wistar rats

机译:维生素A和维生素E对二氧化钛纳米粒子诱导雄性Wistar大鼠肝脏诱导毒性的影响

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The increasing application of titanium dioxide nanoparticles (NTiO2) in life and the toxicity potential of these nanoparticles have raised concerns about their detrimental effects on human health. This study was conducted to investigate the hepatoprotective effects of vitamin E and vitamin A against hepatotoxicity induced by NTiO2 in rats. Thirty-six male Wistar rats were randomly divided into six groups of six rats each. Intoxicated group received 300mg/kg NTiO2 for two weeks by gavage. Groups treated with vitamin E (100IU/kg), vitamin A (100IU/kg) and mixture of these vitamins were orally administered for 3weeks (started 7days before NTiO2 administration). In order to investigate the redox changes, total antioxidant capacity, total oxidant status, and lipid peroxidation were determined in liver tissue as well as activity of antioxidant enzymes including superoxide dismutase, glutathione peroxidase, and catalase. In addition, inflammatory responses were assessed by measuring the expression of NF-B (mRNA) and TNF- (mRNA and protein). Histopathological analysis and measurement of liver enzymes (ALP, ALT, AST, and LDH in serum) were also done to determine hepatic injury. In liver, NTiO2 caused hepatic injury, redox perturbation, and reduction of antioxidant enzymes and elevation of inflammatory mediators, significantly. However, treatment with vitamins was able to significantly ameliorate these alterations. This study highlights the antioxidant and anti-inflammatory properties of vitamins A and E against toxicity of NTiO2 and poses the use of these vitamins to mitigate the toxic effects of this nanoparticles in NTiO2-contained products.
机译:在这些纳米粒子的生命中越来越多的二氧化钛纳米颗粒(NtiO 2)的应用以及对其对人体健康的不利影响的担忧提高了担忧。进行该研究以研究维生素E和维生素A对大鼠NTIO2诱导的肝毒性的肝保护作用。将三十六只雄性Wistar大鼠随机分为六组六组。醉酒组通过饲养饲养300mg / kg ntio2两周。用维生素E(100IU / kg),维生素A(100iu / kg)和这些维生素的混合物治疗的基团被口服给予3周(NTIO2给药前7天开始)。为了研究氧化还原,在肝组织中确定总抗氧化能力,总氧化剂状态和脂质过氧化,以及抗氧化酶的活性,包括超氧化物歧化酶,谷胱甘肽过氧化物酶和过氧化氢酶。此外,通过测量NF-B(mRNA)和TNF-(mRNA和蛋白)的表达来评估炎症反应。还进行了肝酶(血清中ALP,ALT,AST和LDH的组织病理学分析和测量以确定肝损伤。在肝脏中,NTIO2引起肝损伤,氧化还原扰动和减少抗氧化酶和炎症介质的升高,显着显着。然而,使用维生素的治疗能够显着改善这些改变。本研究突出了维生素A和E对NTIO2毒性的抗氧化剂和抗炎特性,并造成这些维生素的使用,以减轻该纳米颗粒在NTIO2含有产物中的毒性作用。

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