紫茎草可能的预防作用。一些神经退行性疾病的精油

N. Sahakyan, M. Petrosyan
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引用次数: 1

摘要

本文介绍了采自亚美尼亚高原的紫皮草精油(EO)对小胶质细胞系(BV-2野生型(WT)和酰基辅酶a氧化酶1 (ACOX1 - / -)缺陷(ACOX1 - / -)细胞)作用的一些特点。突变细胞系被用作研究EO处理后细胞氧化损伤的模型。在亚美尼亚高海拔地区收获的植物中,提取物的主要成分为普莱酮、异薄荷酮、1,8-桉叶脑、胡椒酮和新薄荷酚,其含量分别为42.1%、9.7%、8.22%、7.35%和5.9%。DPPH法中EO的IC50值为7.025µL/mL。两种细胞系的亚细胞毒浓度(基于MTT法)均为5 × 10-1µL/mL。经EO处理24 h后,WT细胞过氧化氢酶活性降低,而Acox1 - / - BV-2细胞过氧化氢酶活性升高。在治疗72小时时,ACOX1活性降低(高达49%)。这些结果表明,所测试的EO对Acox1 - / -突变细胞有保护作用。
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Possible Preventive Effect of Ziziphora clinopodioides Lam. Essential Oil on Some Neurodegenerative Disorders
The present article describes some characteristics of the effect of essential oil (EO) extracted from Ziziphora clinopodioides harvested from Armenian highlands on microglial cell lines (BV-2 wild-type (WT) and acyl-CoA oxidase1 (ACOX1)-deficient (Acox1–/–) cells). The mutant cell line was used as a model to investigate cellular oxidative damage following EO treatment. The main components of the tested EO were pulegone, isomenthone, 1,8-cineole, piperitone, and neomenthole, with concentrations of 42.1%, 9.7%, 8.22%, 7.35%, and 5.9%, respectively, in plants harvested from the high-altitude Armenian landscape. The IC50 value of the EO in the DPPH assay was 7.025 µL/mL. The sub-cytotoxic concentrations (based on the MTT assay) for both cell lines were 5 × 10–1 µL/mL. The catalase activity of the WT cells was decreased following 24-h treatment with the EO, but that of Acox1–/– BV-2 cellswas increased. ACOX1 activity was decreased (up to 49%) at 72hof treatment. These results show the protective effect of the tested EO on Acox1–/– mutantcells.
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