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萜品油烯在大鼠脑细胞中的抗癌和抗氧化特性。

Anticancer and antioxidant properties of terpinolene in rat brain cells.

作者信息

Aydin Elanur, Türkez Hasan, Taşdemir Sener

出版信息

Arh Hig Rada Toksikol. 2013 Sep;64(3):415-24. doi: 10.2478/10004-1254-64-2013-2365.

DOI:10.2478/10004-1254-64-2013-2365
PMID:24084350
Abstract

Terpinolene (TPO) is a natural monoterpene present in essential oils of many aromatic plant species. Although various biological activities of TPO have been demonstrated, its neurotoxicity has never been explored. In this in vitro study we investigated TPO's antiproliferative and/or cytotoxic properties using the 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyltetrazolium bromide (MTT) test, genotoxic damage potential using the single-cell gel electrophoresis (SCGE), and oxidative effects through total antioxidant capacity (TAC) and total oxidative stress (TOS) in cultured primary rat neurons and N2a neuroblastoma cells. Dose-dependent effects of TPO (at 10 mg L(-1), 25 mg L(-1), 50 mg L(-1), 100 mg L(-1), 200 mg L(-1), and 400 mg L(-1)) were tested in both cell types. Significant (P<0.05) decrease in cell proliferation were observed in cultured primary rat neurons starting with the dose of 100 mg L(-1) and in N2a neuroblastoma cells starting with 50 mg L(-1). TPO was not genotoxic in either cell type. In addition, TPO treatment at 10 mg L(-1), 25 mg L(-1), and 50 mg L(-1) increased TAC in primary rat neurons, but not in N2a cells. However, at concentrations above 50 mg L(-1) it increased TOS in both cell types. Our findings clearly demonstrate that TPO is a potent antiproliferative agent for brain tumour cells and may have potential as an anticancer agent, which needs to be further studied.

摘要

萜品油烯(TPO)是一种天然单萜,存在于许多芳香植物物种的精油中。尽管已证明TPO具有多种生物活性,但其神经毒性从未被研究过。在这项体外研究中,我们使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)试验研究了TPO的抗增殖和/或细胞毒性特性,使用单细胞凝胶电泳(SCGE)研究了其遗传毒性损伤潜力,并通过总抗氧化能力(TAC)和总氧化应激(TOS)研究了其在原代培养大鼠神经元和N2a神经母细胞瘤细胞中的氧化作用。在两种细胞类型中测试了TPO(浓度为10 mg L(-1)、25 mg L(-1)、50 mg L(-1)、100 mg L(-1)、200 mg L(-1)和400 mg L(-1))的剂量依赖性效应。在原代培养大鼠神经元中,从100 mg L(-1)的剂量开始观察到细胞增殖显著(P<0.05)下降,在N2a神经母细胞瘤细胞中,从50 mg L(-1)的剂量开始观察到细胞增殖显著下降。TPO在两种细胞类型中均无遗传毒性。此外,10 mg L(-1)、25 mg L(-1)和50 mg L(-1)的TPO处理可增加原代大鼠神经元中的TAC,但对N2a细胞无此作用。然而,在浓度高于50 mg L(-1)时,它会增加两种细胞类型中的TOS。我们的研究结果清楚地表明,TPO是一种有效的脑肿瘤细胞抗增殖剂,可能具有作为抗癌剂的潜力,这需要进一步研究。

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