EDST-AZM-center and Lebanese University, Faculty of Sciences I, Rafic Hariri Campus, Hadath, Lebanon.
Lebanese American University- Faculty of Arts and Sciences, Department of Natural Sciences, Byblos, Lebanon.
Drug Chem Toxicol. 2022 May;45(3):1168-1179. doi: 10.1080/01480545.2020.1810261. Epub 2020 Aug 26.
x L., which belongs to the family, has been reported in the literature for its antioxidant properties in acellular chemical-antioxidant assays. Chlorpromazine (CPZ) is an antipsychotic drug known to cause adverse reactions in humans. Oxidative stress is among the main mechanisms by which CPZ exerts its toxicity in animal cell models as well as in the yeast . In this study we investigated the protective effects of L. crude extracts against CPZ toxicity. We demonstrated that methanolic extracts from rhizome (R-M), leaf (L-M) and flower (Fl-M) had potent antioxidant activity by scavenging the free radical DPPH, with half-maximal effective concentrations (EC) 193, 107, and 174 µg/mL, respectively. R-M, L-M and Fl-M at doses up to 1000 µg/mL, didn't affect yeast cell growth. In addition, we demonstrated for the first time that L-M at 1000 µg/mL and R-M at all tested doses counteracted CPZ toxicity, probably by promoting yeast cell antioxidant agents. The R-M capacity to counteract CPZ toxicity was lost in the yeast strain mutant in catalase-encoding gene (Cta1), while strains mutant in Sod2, Skn7 and Rap1 showed mild or full R-M-induced protective effect against CPZ toxicity. Our results demonstrated that L. R-M extract counteracted CPZ toxicity in the yeast cell model. Further studies are planned to isolate the involved bioactive compounds and identify the involved genes and the antioxidant agents.
x L.,属于 科,其在非细胞化学抗氧化测定中具有抗氧化特性,这在文献中有报道。氯丙嗪(CPZ)是一种抗精神病药物,已知会在人类中引起不良反应。氧化应激是 CPZ 在动物细胞模型以及酵母中发挥毒性的主要机制之一。在这项研究中,我们研究了 L. 粗提取物对 CPZ 毒性的保护作用。我们证明,根茎(R-M)、叶(L-M)和花(Fl-M)的甲醇提取物通过清除自由基 DPPH 具有很强的抗氧化活性,半数最大有效浓度(EC)分别为 193、107 和 174μg/mL。R-M、L-M 和 Fl-M 在高达 1000μg/mL 的剂量下不影响酵母细胞生长。此外,我们首次证明,L-M 在 1000μg/mL 及所有测试剂量的 R-M 可拮抗 CPZ 毒性,可能是通过促进酵母细胞抗氧化剂实现的。在编码过氧化氢酶基因(Cta1)突变的酵母菌株中,R-M 拮抗 CPZ 毒性的能力丧失,而 Sod2、Skn7 和 Rap1 突变菌株对 CPZ 毒性显示出轻度或完全的 R-M 诱导保护作用。我们的结果表明,L. R-M 提取物在酵母细胞模型中拮抗 CPZ 毒性。计划进一步研究以分离相关的生物活性化合物,并鉴定涉及的基因和抗氧化剂。