1. Screening compounds of Chinese medicinal herbs anti-Marek's disease virus.
- Author
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Sun Y, Niu L, Song M, Zhao X, Sun N, He J, Wu C, Jiang J, Bai Y, Guo J, and Li H
- Subjects
- Animals, Apoptosis drug effects, Cells, Cultured, Chick Embryo, Dose-Response Relationship, Drug, Drugs, Chinese Herbal pharmacology, Fibroblasts cytology, Fibroblasts drug effects, Fibroblasts virology, Glycyrrhizic Acid isolation & purification, Herpesvirus 2, Gallid physiology, Phenanthrenes isolation & purification, Solvents chemistry, Virus Replication drug effects, Antiviral Agents pharmacology, Drugs, Chinese Herbal chemistry, Glycyrrhizic Acid pharmacology, Herpesvirus 2, Gallid drug effects, Phenanthrenes pharmacology
- Abstract
Context: Marek's disease (MD) seriously threatens the world poultry industry and has resulted in great economic losses. Chinese medicinal herbs are a rich source for lead compounds and drug candidates for antiviral treatments., Objective: To investigate the anti-MDV activity and mechanism of 20 compounds extracted from Chinese medicinal herbs., Materials and Methods: Antiviral assay, time of addition experiments, and virucidal assay were performed on chicken embryo fibroblast cells. The 50% cytotoxic concentration and 50% effective concentration were determined and, accordingly, selectivity index and inhibition ratio were calculated., Results: Antiviral assay showed dipotassium glycyrrhizinate (DG) and sodium tanshinone IIA sulfonate (STS) exhibited significantly inhibitory activity against MDV in a dose-dependent manner. EC50 of DG and STS were 893.5 ± 36.99 µg/mL and 54.82 ± 2.99 µg/mL, and selective index (SI) were >3.36 and >9.12, respectively. Time of addition experiment and virucidal assay demonstrated DG inhibited viral replication in the full replication cycle and inactivated MDV particles in non-time-dependent manner, but STS interfered with the early stage of MDV replication and inactivated MDV particles in a time-dependent manner. Moreover, both DG and STS promoted apoptosis of cells infected by MDV., Discussion and Conclusion: DG and STS have great potential for developing new anti-MDV drugs for clinic application.
- Published
- 2014
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