Department of Hepatitis and AIDS, Pasteur Institute of Iran, Tehran, Iran.
Indian J Pharmacol. 2012 Jul-Aug;44(4):448-53. doi: 10.4103/0253-7613.99301.
Setarud (IMOD™) is a herbal medicine with beneficial effect for patients suffering Human immunodeficiency virus (HIV) infection and has been approved for IV (intra venues) injection. The beneficial effect of IMOD administration for acquired immune deficiency syndrome (AIDS) patient has been proved in previous clinical trials. Here the in vitro inhibitory effect of IMOD against HIV-1, Herpes simplex virus (HSV) and murine leukemia viruses (MLV) was evaluated.
HIV single cycle replication and HSV plaque reduction assays were used to evaluate the anti-viral effect. The level of HIV replication was monitored by p24 capture Enzyme-linked immunosorbent assay (ELISA). The single round infection [with green fluorescent protein (GFP) reporter MLV and HIV], virucidal and time-of-additions (HSV) assays were utilized to determine the mode of anti-viral activity. The toxicity of IMOD for cells was monitored by XTT (sodium 3_-[1 (phenylaminocarbonyl)- 3,4-tetrazolium]-bis (4-methoxy-6-nitro)benzene sulfonic acid) cell proliferation assay kit.
IMOD inhibited 50% of HIV-1 and HSV replication (IC(50)) at 6.5 × 10(-4) and 4.3 × 10(-3)V/V concentrations, respectively. The IC(50) value against HIV-1 and MLV infection were 6 × 10(-4)V/V and 4.9 × 10(-4)V/V. Virucidal assay showed that IMOD reduces the potency of HIV and HSV particles to 41 and 54% of control, respectively. Time-of-addition study revealed that IMOD inhibits the replication of HSV at a stage after penetration of virions to the target cells.
Data from this study indicate that IMOD has significant anti-viral activity against HIV, HSV and MLV. Setarud could be subjected to further investigation after isolation of the constituents and determination of the toxic components.
Setarud(IMOD™)是一种草药,对人类免疫缺陷病毒(HIV)感染患者有有益的影响,已被批准用于静脉注射(IV)。先前的临床试验已经证明,IMOD 对获得性免疫缺陷综合征(AIDS)患者的有益作用。在此,评估了 IMOD 对 HIV-1、单纯疱疹病毒(HSV)和鼠白血病病毒(MLV)的体外抑制作用。
使用 HIV 单周期复制和 HSV 蚀斑减少测定法来评估抗病毒作用。通过 p24 捕获酶联免疫吸附测定(ELISA)监测 HIV 复制水平。利用带有绿色荧光蛋白(GFP)报告基因的 MLV 和 HIV 的单次感染、病毒杀灭和添加时间(HSV)测定法来确定抗病毒活性模式。通过 XTT(对苯二甲脒基-3,4-四唑鎓-5-(4-甲氧基-6-硝基)-2,4-二磺酸二钠盐)细胞增殖测定试剂盒监测 IMOD 对细胞的毒性。
IMOD 抑制 50%的 HIV-1 和 HSV 复制(IC50)的浓度分别为 6.5×10-4 和 4.3×10-3V/V。对 HIV-1 和 MLV 感染的 IC50 值分别为 6×10-4V/V 和 4.9×10-4V/V。病毒杀灭测定表明,IMOD 将 HIV 和 HSV 颗粒的效力降低至对照的 41%和 54%。添加时间研究表明,IMOD 在病毒颗粒穿透靶细胞后抑制 HSV 的复制。
本研究数据表明,IMOD 对 HIV、HSV 和 MLV 具有显著的抗病毒活性。在分离成分和确定有毒成分后,Setarud 可以进一步研究。