Ascorbate and Alpha-Tocopherol Mitigate Toxic Pathological Changes in Adult Wistar Rats Exposed to Cypermethrin

Temidayo Daniel Adeniyi, Akinpelu Moronkeji, Osetohanmen Flourish Ralph-Okhiria
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Abstract

Excessive and uncontrolled use of pyrethroids such as cypermethrin (CYP) for pest control in Nigeria can adversely affect humans. This study investigated the oxidative stress response to cypermethrin exposure as well as the therapeutic effect of ascorbate and alpha-tocopherol when administered singly or co-administered. Additionally, the lungs and heart of the exposed animals were histologically assessed for cypermethrin-induced cytopathic changes. Twenty-five adult male Wistar rats weighing between 180 – 200g were randomly assigned to five groups of five animals each. Group I was the unexposed control group, while Group II was the exposed untreated group that was orally administered Cypermethrin at a dose of 10mg/kg/bw. Group III – V was given cypermethrin at standard doses of 10mg/kg/bw, and orally administered with ascorbate (5000mg/kg/bw), alpha-tocopherol (3000mg/kg/bw) and co-administration of ascorbate and alpha-tocopherol (5000mg/kg/bw and 3000mg/kg/bw) respectively. Animals were euthanized after 28 days, and samples were processed for histological and biochemical studies. The results showed elevated malondialdehyde (MDA) levels with a concurrent marked decrease in superoxide dismutase (SOD), glutathione peroxidase (GPx), and catalase (CAT) activities (p<0.05) in the cypermethrin-exposed untreated rats, while histopathological findings revealed inflammation and congestion in the organs studied. The co-administrative treatment with ascorbate and alpha-tocopherol better restores biochemical parameters than their single administration. Conclusively, co-administration of ascorbic acid and alpha-tocopherol ameliorates cypermethrin-induced oxidative damage better than single administration, which may be due to their synergistic antioxidant properties.
抗坏血酸和α-生育酚减轻暴露于氯氰菊酯的成年 Wistar 大鼠的毒性病理变化
在尼日利亚,过量和无节制地使用氯氰菊酯(CYP)等拟除虫菊酯来控制害虫会对人体产生不利影响。本研究调查了接触氯氰菊酯后的氧化应激反应,以及抗坏血酸和α-生育酚单独或联合给药的治疗效果。此外,还对暴露动物的肺部和心脏进行了组织学评估,以确定是否存在氯氰菊酯诱导的细胞病理变化。25 只成年雄性 Wistar 大鼠体重在 180 - 200 克之间,被随机分配到五组,每组五只。第一组为未暴露对照组,第二组为暴露未处理组,口服氯氰菊酯的剂量为 10 毫克/千克/体重。第三至第五组分别按标准剂量(10 毫克/千克/体重)和抗坏血酸(5000 毫克/千克/体重)、α-生育酚(3000 毫克/千克/体重)口服氯氰菊酯,以及抗坏血酸和α-生育酚联合给药(5000 毫克/千克/体重和 3000 毫克/千克/体重)。动物在 28 天后安乐死,并对样本进行组织学和生化研究。结果显示,在氯氰菊酯暴露的未处理大鼠中,丙二醛(MDA)水平升高,同时超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)和过氧化氢酶(CAT)活性明显降低(p<0.05),而组织病理学结果显示,所研究的器官出现炎症和充血。同时服用抗坏血酸和α-生育酚能更好地恢复生化指标,而不是单一服用。最后,抗坏血酸和α-生育酚联合给药比单一给药能更好地改善氯氰菊酯诱导的氧化损伤,这可能是由于它们具有协同抗氧化特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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