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New insights into antioxidant strategies against paraquat toxicity

机译:抗百草枯毒性的抗氧化剂策略的新见解

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Paraquat (PQ, 1,1'-dimethyl-4-4'-bipyridinium dichloride) is a highly toxic quaternary ammonium herbicide widely used in agriculture, it exerts its toxic effects mainly because of its redox cycle through the production of superoxide anions in organisms, leading to an imbalance in the redox state of the cell causing oxidative damage and finally cell death. The contribution of mitochondrial dysfunction including increased production of reactive oxygen species besides the reduction in oxygen consumption as well as in the activity of some respiratory complexes has emerged as a key component in the mechanisms through which PQ induces cell death. Although several aspects of PQ-mitochondria interaction remain to be clarified, recent advances have been conducted with reproducible results. Currently, there is no treatment for PQ poisoning; however, several studies taking into account oxidative stress as the main mechanism of PQ-induced toxicity suggest an antioxidant therapy as a viable alternative. In fact, it has been shown that the antioxidants naringin, sylimarin, edaravone, Bathysa cuspidata extracts, alpha-lipoic acid, pirfenidone, lysine acetylsalicylate, selenium, quercetin, C-phycocyanin, bacosides, and vitamin C may be useful in the treatment against PQ toxicity. The main mechanisms involved in the protective effect of these antioxidants include the reduction of oxidative stress and inflammation and the induction of antioxidant defenses. Interestingly, recent findings suggest that the induction of nuclear factor erythroid like-2 (Nrf2), a major regulator of the antioxidant response, by some of the above-mentioned antioxidants, has been involved in the protective effect against PQ-induced toxicity.
机译:百草枯(PQ,1,1'-二甲基-4-4'-联吡啶二氯化物)是一种剧毒的季铵盐除草剂,广泛用于农业中,它发挥毒性作用的主要原因是它通过在生物体中产生超氧阴离子而产生氧化还原循环。导致细胞氧化还原状态的失衡,导致氧化损伤,最终导致细胞死亡。线粒体功能障碍的贡献包括增加活性氧的产生,以及减少氧气消耗以及某些呼吸复合物的活性,这已成为PQ诱导细胞死亡的机制中的关键组成部分。尽管PQ-线粒体相互作用的几个方面尚待阐明,但最近的进展已经取得了可重复的结果。目前,没有针对PQ中毒的治疗方法;然而,几项将氧化应激作为PQ诱导毒性的主要机制的研究表明,抗氧化剂治疗是可行的选择。实际上,已经证明,抗氧化剂柚皮苷,sylimarin,依达拉奉,Bathysa cuspidata提取物,α-硫辛酸,吡非尼酮,赖氨酸乙酰水杨酸酯,硒,槲皮素,C-藻蓝蛋白,ba糖和维生素C可用于治疗PQ毒性。这些抗氧化剂的保护作用涉及的主要机制包括减少氧化应激和炎症以及诱导抗氧化剂防御。有趣的是,最近的发现表明,通过上述某些抗氧化剂对抗氧化剂响应的主要调节剂核因子类红细胞样2(Nrf2)的诱导,已参与了针对PQ诱导的毒性的保护作用。

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