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RESEARCH ARTICLE |
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Year : 2011 | Volume
: 43
| Issue : 5 | Page : 536-540 |
Evaluation of Cynanchum otophyllum glucan sulfate against human immunodeficiency virus and herpes simplex virus as a microbicide agent
Jian Tao1, Jing Yang2, Chaoyin Chen3, Xiaomei Cao4, Shenglan Zhao5, Kunlong Ben4
1 Department of Pharmacology, Kunming University, Yunnan; Laboratory of Cell and Molecular Immunology, Kunming Institute of Zoology, Chinese Academy of Sciences, Yunnan, China 2 Laboratory of Cell and Molecular Immunology, Kunming Institute of Zoology, Chinese Academy of Sciences, Yunnan; Department of Chemical Processing of Forest Products, Southwest Forestry University, Yunnan, China 3 Department of Life Science and Technology, Kunming University of Science and Technology, Yunnan, China 4 Laboratory of Cell and Molecular Immunology, Kunming Institute of Zoology, Chinese Academy of Sciences, Yunnan, China 5 Department of Chinese Materia Medica, Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan, China
Correspondence Address:
Kunlong Ben Laboratory of Cell and Molecular Immunology, Kunming Institute of Zoology, Chinese Academy of Sciences, Yunnan China
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0253-7613.84967
Objective : The root ofCynanchum otophyllum -also known as Qing Yang Sheng-is a traditional ethnical Chinese medicine. The objective of this study was to evaluate in vitro activities and safety of C. otophyllum glucan sulfate (PS20) against Human Immunodeficiency Virus (HIV) and Herpes Simplex Virus (HSV). Materials and Methods : Anti-HIV activity was detected with syncytial formation assay and quantitative P24 Enzyme-Linked Immunosorbent Assay (ELISA). Anti-HSV activity was detected with plaque reduction assay; cytotoxicity was tested with MTT colorimetric assay; and anti-bacterial activity was tested with microdilution method. Anti-HIV mechanism was investigated with fusion inhibition, time of addition, and pretreatment. Results : The 50% Inhibition Concentration (IC 50 ) of PS20 for HIV-1 IIIB , HIV- Ada-M , HIV-1 Bal , HSV-I, and -II were 0.26 ± 0.02 mM, 0.46 ± 0.02 mM, 0.90 ± 0.04 mM, 3.45 ± 0.85 mM, and 0.70 ± 0.22 mM, respectively. Selectivity Indices (SI) were 653, 50, 39, 85, and 362, respectively. Studies on anti-HIV mechanism of PS20 showed that the target molecule should be the envelope protein. The 50% Cytotoxicity Concentrations (CC 50 ) of PS20 for HeLa and ME-180 cell lines and human foreskin fibroblast cells was more than 70 mM. The Minimum Inhibitory Concentration (MIC) for vaginal lactobacilli was more than 1000 mM. Conclusion : PS20 possesses anti-HIV and HSV effect and low cytotoxicity to epithelium cells and vaginal lactobacilli. It may be considered as a potential microbicide agent for further investigation.
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