College of Animal Science and Veterinary Medicine, Shanxi Agricultural University, Taigu, Shanxi 030801, P.R. China.
Pharm Biol. 2013 Sep;51(9):1137-43. doi: 10.3109/13880209.2013.781197. Epub 2013 Apr 22.
The prevalence of infectious bursal disease has brought about enormous financial losses to the world poultry industry. Chinese herb medicines can provide valuable materials for discovery and development of new drugs.
To screen constituents derived from Chinese herb medicines for their antiviral activity against infectious bursal disease virus (IBDV) in vitro.
Twenty constituents derived from Chinese herb medicines and B87 strain of IBDV were used. The 50% cytotoxic concentration (CC₅₀) and 50% effective concentration (EC₅₀) were determined by visualization of cytopathologic effect (CPE) and 3-(4,5-dimethyithiazol-2-yl)-2,5-diphenyltetrazoliumbromide (MTT) test on chicken embryo fibroblast. Selectivity index (SI) and inhibition ratio (%I) were calculated from the data obtained from the MTT test.
Antiviral assays showed dipotassium glycyrrhizinate and ligustrazine hydrochloride among the 20 constituents tested exhibited significant inhibitory activity against IBDV in a dose-dependent manner. EC₅₀ of dipotassium glycyrrhizinate and ligustrazine hydrochloride were 663.2 ± 268.4 and 92.52 ± 21.13 µg/mL, and SI were >4.52 and >21.62, respectively. The time-of-addition and virucidal assay indicated that anti-IBDV activity of the two constituents could be due to their inhibiting virus replication and/or inactivating virus directly. The inhibition of virus attachment was not observed in the adsorption inhibition assay. Dipotassium glycyrrhizinate and ligustrazine hydrochloride exhibited more than 70% and 80% inhibition of IBDV, respectively, at the maximum safe concentration.
We believe that dipotassium glycyrrhizinate and ligustrazine hydrochloride can be used to develop a new anti-IBDV compound, and it is worth applying the constituents in clinical practice.
传染性法氏囊病的流行给世界家禽业带来了巨大的经济损失。中草药可为新药的发现和开发提供有价值的材料。
筛选中草药来源的成分,研究其对传染性法氏囊病病毒(IBDV)的体外抗病毒活性。
采用 20 种中草药来源的成分和 B87 株 IBDV。通过观察细胞病变效应(CPE)和 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴盐(MTT)试验,确定 50%细胞毒性浓度(CC₅₀)和 50%有效浓度(EC₅₀)。根据 MTT 试验数据计算选择指数(SI)和抑制率(%I)。
抗病毒测定表明,在 20 种测试成分中,二钾甘草酸和盐酸川芎嗪呈剂量依赖性方式对 IBDV 表现出显著的抑制活性。二钾甘草酸和盐酸川芎嗪的 EC₅₀分别为 663.2±268.4 和 92.52±21.13µg/mL,SI 分别为>4.52 和>21.62。时程添加和病毒灭活试验表明,两种成分的抗 IBDV 活性可能是由于其抑制病毒复制和/或直接使病毒失活所致。在吸附抑制试验中未观察到病毒附着抑制。在最大安全浓度下,二钾甘草酸和盐酸川芎嗪对 IBDV 的抑制率分别超过 70%和 80%。
我们认为二钾甘草酸和盐酸川芎嗪可用于开发新型抗 IBDV 化合物,值得将这些成分应用于临床实践。