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Antimutagenicity of Methanolic Extracts from Anemopsis californica in Relation to Their Antioxidant Activity

机译:加州小脚草甲醇提取物的抗诱变性与其抗氧化活性的关系

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摘要

Anemopsis californica has been used empirically to treat infectious diseases. However, there are no antimutagenic evaluation reports on this plant. The present study evaluated the antioxidant activity in relation to the mutagenic and antimutagenic activity properties of leaf (LME) and stem (SME) methanolic extracts of A. californica collected in the central Mexican state of Querétaro. Antioxidant properties and total phenols of extracts were evaluated using DPPH (1,1-diphenyl-2-picrylhydrazyl) and Folin-Ciocalteu methods, respectively. Mutagenicity was evaluated using the Ames test employing Salmonella enterica serovar Typhimurium strains (TA98, TA100, and TA102), with and without an aroclor 1254 (S9 mixture). Antimutagenesis was performed against mutations induced on the Ames test with MNNG, 2AA, or 4NQO. SME presented the highest antioxidant capacity and total phenolic content. None of the extracts exhibited mutagenicity in the Ames test. The extracts produced a significant reduction in 2AA-induced mutations in S. typhimurium TA98. In both extracts, mutagenesis induced by 4NQO or methyl-N′-nitro-N-nitrosoguanidine (MNNG) was reduced only if the exposure of strains was <10 μg/Petri dish. A. californca antioxidant properties and its capacity to reduce point mutations render it suitable to enhance medical cancer treatments. The significant effect against antimutagenic 2AA suggests that their consumption would provide protection against carcinogenic polycyclic aromatic compounds.
机译:加州按蚊(Anemopsis californica)已凭经验用于治疗传染病。但是,没有关于该植物的抗突变评估报告。本研究评估了在墨西哥中部克雷塔罗州收集的加州产烟曲霉的叶片(LME)和茎(SME)甲醇提取物的诱变和抗诱变活性,并评估了其抗氧化活性。分别使用DPPH(1,1-二苯基-2-picylhydrazyl)和Folin-Ciocalteu方法评估提取物的抗氧化性能和总酚。使用Ames试验评估致突变性,该试验采用沙门氏菌血清型鼠伤寒沙门氏菌菌株(TA98,TA100和TA102),有或没有aroclor 1254(S9混合物)。针对由MNNG,2AA或4NQO在Ames测试中诱导的突变进行抗诱变。中小企业表现出最高的抗氧化能力和总酚含量。在Ames试验中,所有提取物均未显示出致突变性。提取物使鼠伤寒沙门氏菌TA98中2AA诱导的突变显着减少。在两种提取物中,仅当菌株的暴露量小于10μg/ Petri培养皿时,由4NQO或甲基-N'-硝基-N-亚硝基胍(MNNG)诱导的诱变才会减少。 A. californca的抗氧化特性及其减少点突变的能力使其适合增强医学癌症治疗。针对抗诱变剂2AA的显著作用表明,它们的消费将提供针对致癌多环芳族化合物的保护。

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