合穗蓼提取物对单纯疱疹病毒1型的抗病毒活性研究

Nur Sahira Mohd Jaafar, Noor Zarina Abd Wahab
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引用次数: 0

摘要

1型单纯疱疹病毒(HSV-1)是人类疱疹病毒α亚家族的一部分。几种抗病毒药物可用于治疗1型单纯疱疹病毒,通常是一线抗病毒药物,如阿昔洛韦(ACV)。但是已有几例关于ACV对HSV耐药的报道,因此,研究人员倾向于从植物提取物中开发抗病毒药物。紫苏是传统上被用作药物的植物之一,它含有丰富的生物活性化合物,包括精油、萜类、单宁和类黄酮。这些植物化学化合物具有很强的抗氧化作用,可以帮助抑制病毒基因组复制,从而使病毒脂质包膜[2]失效。本研究的目的是测定多花楸甲醇提取物的细胞毒浓度(CC50)和抗病毒活性。采用[3]描述的方法进行细胞毒性测定。利用微孔板读卡器(Infinite M200 Pro)分析吸光度读数。50%细胞毒性浓度(CC50)定义为与未处理的细胞相比,能够使细胞活力降低50%的样品浓度。通过三种不同的处理[3],即处理后、预处理和杀病毒试验,采用斑块减少试验来观察其抗病毒活性。根据图1,使用MTT法对Vero细胞进行细胞毒性筛选显示,提取物的CC50值为0.135 mg/mL,不属于细胞毒性化合物的范围。任何CC50或IC50低于4µg/mL的物质被认为是活性细胞毒作用[4]。从图2中可以看出,处理后的抗hsv -1活性最高,其EC50和SI值分别为0.015mg/mL和9.03。在2小时的孵育后,提取物显示出对减少HSV-1复制的轻微有效,这可能是由于在附着的早期阶段抑制。预处理后的EC50和SI值分别为0.019 mg/mL和7.12,表明提取物在复制发生前对HSV-1的附着具有中等抑制作用。这可能发生在Vero细胞与提取物结合时,这种提取物会干扰细胞膜的糖蛋白受体,从而阻止HSV-1附着在细胞表面。抑毒实验的EC50和SI值分别为0.018 mg/mL和7.28,对病毒复制具有中等抑制作用。在这项研究中,多花葡萄球菌已被证明能在30分钟内直接灭活HSV-1病毒粒子。SI值大于10 (SI>10)表明任何抗菌化合物具有成为抗病毒治疗剂[6]的效力。总之,本研究结果表明,多花参提取物似乎具有中等抗病毒作用,对Vero细胞无毒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antiviral Activity of Syzygium polyanthum Extract against Herpes Simplex Virus-Type 1 (HSV-1)
Herpes simplex virus type 1 (HSV-1) is part of the alpha subfamily of human herpesviruses. Several antiviral medications can be prescribed for treating HSV-1 which is usually first line antiviral agents such as acyclovir (ACV). But there are several cases that have been reported on ACV resistance to HSV, thus, researchers tend to develop the antiviral agent from plants extract. Syzygium polyanthum is one of the plants that has been traditionally used as a drug which is rich in bioactive compounds, including essential oils, terpenoids, tannins, and flavonoids [1]. These phytochemical compounds, which have strong antioxidant action, can aid in the inhibition of viral genome replication which disables the viral lipid envelope [2].   The objective of this study is to determine the cytotoxic concentration (CC50) and antiviral activity of S. polyanthum methanolic extract. Cytotoxicity was performed using the method described by [3]. The absorbance readings were analysed using microplate reader (Infinite M200 Pro). The 50% cytotoxicity concentration (CC50) was defined as the sample concentration that able to reduce 50% of cell viability compared to the untreated cells. Antiviral activity was performed by using plaque reduction assay with three different treatments [3] which are post- treatment, pre-treatment and virucidal assay.   Based on Figure 1, cytotoxicity screening against Vero cells using MTT assay showed that the CC50 values for extract was 0.135 mg/mL which considered not in the range of cytotoxic compounds. Any CC50 or IC50 of a substance less than 4 µg/mL was considered an active cytotoxic effect [4]. Based on Figure 2, post treatment assay showed the most anti-HSV-1 activity of S. polyanthum extract which the EC50 and SI value were 0.015mg/mL and 9.03, respectively. The extract showed to be slightly effective in reducing HSV-1 replication after 2-hour incubation which might be due to the inhibition in the early phase of the attachment. For pre-treatment, EC50 and SI values were 0.019 mg/mL and 7.12, which the extract showed to be moderately effective in inhibiting the attachment of HSV-1 before the replication can occur. This might occur as Vero cells bind to the extract that could interfere with the cell membrane's glycoprotein receptors which prevented HSV-1 from attaching to the cell surface [5]. The EC50 and SI value for virucidal assay was 0.018 mg/mL and 7.28 as the result showed moderately effective inhibited the viral replication. S. polyanthum has been shown to directly inactivate HSV-1 virions within 30 minutes of exposure in this study. An SI value greater than 10 (SI>10) indicates that any antimicrobial compound has the potency to become an antiviral treatment agent [6]. In conclusion, the findings of this study demonstrate that S. polyanthum extract seems to have moderate antiviral  effects and non-toxic to Vero cells.
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