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Synergistic anti-hepatitis C virus activity of Ruta angustifolia extract with NS3 protein inhibitor

  • Tutik Sri Wahyuni EMAIL logo , Humairoh Mahfud , Adita Ayu Permatasari , Aty Widyawaruyanti and Achmad Fuad
Published/Copyright: December 14, 2019

Abstract

Background

Medicinal plants are known to perform many pharmacological actions due to their chemical metabolites, which include antiviral effects. Previously, the extract of Ruta angustifolia was shown to have potential anti-hepatitis C virus (HCV) activity without any cytotoxicity, with a 50% inhibitory concentration of 3.0 μg/mL and a 50% cytotoxicity concentration of >100 μg/mL. Furthermore, the combination of medicinal plants and current anti-HCV agents, such as a direct-acting antiviral agent, was shown to potentiate their overall effectiveness. In the course of this study, the ethanolic extract of R. angustifolia was evaluated for its anti-HCV effects; specifically, the mechanism of action on HCV NS3 and NS5A protease was investigated.

Methods

Analysis of the use of this extract in conjunction with current NS3 inhibitor drugs, simeprevir (SMV) and telaprevir (TVR), was performed. Anti-HCV activity was performed by in vitro culture of hepatocyte cells. The cells were infected and treated with various concentrations of the sample. HCV inhibition was calculated and CompuSyn software analysis was used to determine the synergistic effect of the combination.

Results

Results demonstrated that R. angustifolia extract inhibited the post-entry step and decreased the protein levels of HCV NS3 and NS5A. The combination of extract and SMV and TVR mediated a synergistic effect.

Conclusions

These findings suggest that combining R. angustifolia extract with current anti-HCV drugs should be considered when developing alternative and complementary anti-HCV medicines.

Acknowledgments

The authors are sincerely grateful to Prof. Hak Hotta and Dr. Chie Aoki Utsubo for providing HCV and hepatocyte cells.

  1. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  2. Research funding: None declared.

  3. Competing interests: The authors state no conflict of interest.

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Received: 2019-11-17
Accepted: 2019-11-18
Published Online: 2019-12-14

© 2019 Walter de Gruyter GmbH, Berlin/Boston

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