Anti-viral activity of compounds from Agrimonia pilosa and Galla rhois extract mixture.


Journal

Bioorganic chemistry
ISSN: 1090-2120
Titre abrégé: Bioorg Chem
Pays: United States
ID NLM: 1303703

Informations de publication

Date de publication:
12 2019
Historique:
received: 03 05 2019
revised: 18 09 2019
accepted: 26 09 2019
pubmed: 5 10 2019
medline: 21 10 2020
entrez: 5 10 2019
Statut: ppublish

Résumé

Hepatitis C virus (HCV) infection is a significant health problem, with a worldwide prevalence of about 170 million. Recently, the development of direct acting antiviral (DAA) as a therapeutic agent for HCV has been rapidly increasing. However, DAA has a side effect and is costly. Therefore, it is still necessary to develop a therapeutic agent to treat HCV infection using products. Agrimonia pilosa (AP) and Galla rhois (RG) are traditional medicines and are known to display therapeutic activity on various diseases. Notably, they have been reported to have an anti-viral effect on HBV and influenza virus infections. It is expected that anti-viral activity will increase when two extracts are mixed. To investigate their anti-viral activity, the expression level of HCV Core 1b and NS5A was measured. Remarkably, AP, RG, and their mixed compound (APRG64) strongly inhibited the expression of viral proteins, which led us to identify their metabolites. A total of 14 metabolites were identified using liquid chromatography mass spectrometry (LC-MS). These metabolites were evaluated for their anti-HCV activity to identify active ingredients. In conclusion, our results unveiled that anti-HCV activity of Agrimonia pilosa and Galla rhois extract mixture could lead to the development of a novel therapy for HCV infection.

Identifiants

pubmed: 31585267
pii: S0045-2068(19)30583-8
doi: 10.1016/j.bioorg.2019.103320
pii:
doi:

Substances chimiques

Antiviral Agents 0
Biological Products 0
Galla Rhois 0
Plant Extracts 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

103320

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Jeong Eun Kwon (JE)

Graduate School of Biotechnology and Department of Oriental Medicinal Biotechnology, Kyung Hee University, Yongin 17104, Republic of Korea.

Yeong-Geun Lee (YG)

Graduate School of Biotechnology and Department of Oriental Medicinal Biotechnology, Kyung Hee University, Yongin 17104, Republic of Korea.

Ji-Hun Kang (JH)

Department of Life Science, Chung-Ang University, Seoul 06974, Republic of Korea.

Yun-Feng Bai (YF)

Department of Integrative Medicine, The Fifth Medical Center, Chinese PLA General Hospital, Beijing 100039, China.

Yong Joon Jeong (YJ)

Genencell Co., Ltd, Yongin 16950, Republic of Korea.

Nam-In Baek (NI)

Graduate School of Biotechnology and Department of Oriental Medicinal Biotechnology, Kyung Hee University, Yongin 17104, Republic of Korea.

Young-Jin Seo (YJ)

Department of Life Science, Chung-Ang University, Seoul 06974, Republic of Korea. Electronic address: yjseo@cau.ac.kr.

Se Chan Kang (SC)

Graduate School of Biotechnology and Department of Oriental Medicinal Biotechnology, Kyung Hee University, Yongin 17104, Republic of Korea. Electronic address: sckang@khu.ac.kr.

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Classifications MeSH