Department of Zoology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Department of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Biomolecules. 2019 Jul 7;9(7):261. doi: 10.3390/biom9070261.
Exposure to organophosphorus insecticides causes several health problems to animals and humans. Red beetroot (RBR) is rich in antioxidant ingredients and possesses a promising hepatoprotective activity. This study evaluated the potential of RBR extract to prevent chlorpyrifos (CPF)-induced liver injury, with an emphasis on oxidative stress, inflammation and apoptosis. Rats received 10 mg/kg CPF and were treated with 300 mg/kg RBR extract for 28 days. CPF caused liver injury evidenced by elevated serum levels of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP) and bilirubin, along with several histological alterations. Hepatic lipid peroxidation (LPO) and nitric oxide (NO) levels, as well as inducible nitric oxide synthase (iNOS) and pro-inflammatory cytokines were increased in CPF-intoxicated rats. RBR prevented CPF-induced histological alterations, and ameliorated liver function, LPO, NO, iNOS and pro-inflammatory cytokines. RBR boosted glutathione and antioxidant enzymes, and increased Nrf2 expression. In addition, RBR diminished Bax and caspase-3, and increased Bcl-2 expression. In conclusion, RBR prevented CPF-induced liver injury via attenuation of oxidative stress, inflammation and apoptosis. RBR enhanced antioxidant defenses, suggesting that it could be used as a potential therapeutic intervention to minimize CPF hepatotoxicity.
接触有机磷杀虫剂会对动物和人类造成多种健康问题。红甜菜(RBR)富含抗氧化成分,具有有前景的肝保护活性。本研究评估了 RBR 提取物预防毒死蜱(CPF)诱导的肝损伤的潜力,重点关注氧化应激、炎症和细胞凋亡。大鼠接受 10mg/kg CPF 并接受 300mg/kg RBR 提取物治疗 28 天。CPF 导致血清丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)、碱性磷酸酶(ALP)和胆红素水平升高,表明发生了肝损伤,同时还伴有多种组织学改变。肝脂质过氧化(LPO)和一氧化氮(NO)水平以及诱导型一氧化氮合酶(iNOS)和促炎细胞因子在 CPF 中毒大鼠中增加。RBR 可预防 CPF 诱导的组织学改变,并改善肝功能、LPO、NO、iNOS 和促炎细胞因子。RBR 可增强谷胱甘肽和抗氧化酶,并增加 Nrf2 的表达。此外,RBR 降低了 Bax 和 caspase-3 的表达,增加了 Bcl-2 的表达。总之,RBR 通过减轻氧化应激、炎症和细胞凋亡来预防 CPF 诱导的肝损伤。RBR 增强了抗氧化防御能力,表明它可能被用作减轻 CPF 肝毒性的潜在治疗干预措施。