Protective effects of Butylated Hydroxytoluene (BHT) against sodium Arsenite (NaAsO2) - Induced hepatotoxicity in Wistar Rats

Opeyemi Olaoluwa, Latinwo, Opeyemi Olaoluwa Latinwo, Joseph-Peace Adekanye, Okikijesu Oladokun, Emeka Gabriel Ekeh, Precious Ogundipe, Tella Adedayo, David Effiong Ukem, Paul Gberiye Benibo, Adewale Phillip Adekunle
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Abstract

One of the major environmental contaminants that can be found on a global scale is arsenic. Sodium arsenite (NaAsO2) is one of the compounds of arsenic which is considered very toxic. Long term exposure to NaAsO2 can cause chemical complications in various organs of the body such as the liver, kidney, testes and brain tissues. Butylated hydroxytoluene (BHT) is an antioxidant that can serve as an antitoxic effect. NaAsO2. In this topic, we examined the chemo-protective effect of BHT on NaAsO2 induced hepatotoxicity in male Wistar rats. Wistar rats (n=42, +120g) were randomly grouped into seven treatment groups: of 7 animals each Control 1(corn oil); Control 2(distilled water); NaAsO2 alone (2.5mg/kg). BHT alone (25 mg/kg); BHT only (25mg/kg); BHT+ NaAsO2 (25mg/kg + 2.5/kg), and BHT+ NaAsO2 (2.5g/kg + 50 mg/kg) and treated for 14 days. Markers of liver functions, inflammation, oxidative stress and antioxidant profile of liver were assayed spectrophotometrically. Our results showed that exposure to NaAsO2 resulted in dramatic increase in the levels of AST, ALT and ALP activity Furthermore, NaAsO2 increased the concentration of oxidative stress markers such as xanthine oxidase (XO) and lipid peroxidation (MDA) and inflammatory markers such as myeloperoxidase (MPO) and nitric oxide (NO) with a concomitant decrease in antioxidant markers such as superoxide dismutase (SOD). Glutathione-S-transferase (GST), and catalase. However, the co-exposure of rats to both BHT and NaAsO2 can result in significant decrease the parameters above. In conclusion, exposure of rats to NaAsO2 causes increased inflammatory and oxidative stress signals, but these harmful effects can be ameliorated by administration of antioxidants such as BHT as confirmed by this research.
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丁基羟基甲苯(BHT)对亚砷酸钠(NaAsO2)诱导的 Wistar 大鼠肝毒性的保护作用
砷是全球范围内的主要环境污染物之一。亚砷酸钠(NaAsO2)是砷的化合物之一,被认为具有剧毒。长期接触 NaAsO2 可导致人体各器官(如肝脏、肾脏、睾丸和脑组织)出现化学并发症。丁基羟基甲苯(BHT)是一种抗氧化剂,可以起到解毒作用。NaAsO2。在本课题中,我们研究了 BHT 对 NaAsO2 诱导的雄性 Wistar 大鼠肝毒性的化学保护作用。将 Wistar 大鼠(n=42,+120g)随机分为 7 个治疗组:对照组 1(玉米油);对照组 2(蒸馏水);单独 NaAsO2(2.5mg/kg);单独 BHT(25 mg/kg);对照组 3(玉米油);对照组 4(蒸馏水);单独 NaAsO2(2.5mg/kg)。对照组 1(玉米油);对照组 2(蒸馏水);单独 NaAsO2(2.5mg/kg);单独 BHT(25 mg/kg);仅 BHT(25 mg/kg);BHT+NaAsO2(25 mg/kg + 2.5/kg);BHT+NaAsO2(2.5g/kg + 50 mg/kg),治疗 14 天。用分光光度法检测肝功能、炎症、氧化应激和抗氧化指标。此外,NaAsO2 还增加了黄嘌呤氧化酶 (XO) 和脂质过氧化物 (MDA) 等氧化应激标志物以及髓过氧化物酶 (MPO) 和一氧化氮 (NO) 等炎症标志物的浓度,同时降低了超氧化物歧化酶 (SOD) 等抗氧化标志物的浓度。谷胱甘肽转移酶(GST)和过氧化氢酶。不过,大鼠同时暴露于 BHT 和 NaAsO2 会导致上述参数显著下降。总之,大鼠暴露于 NaAsO2 会导致炎症和氧化应激信号增加,但这些有害影响可以通过服用 BHT 等抗氧化剂得到改善,本研究也证实了这一点。
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