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In Vitro Antiviral Activity of Rhodiola crenulata Extract against Zika Virus and Japanese Encephalitis Virus: Viral Binding and Stability.
Lai, Zheng-Zong; Yen, I-Chuan; Hung, Hao-Yuan; Hong, Chen-Yang; Lai, Chih-Wei; Lee, Yen-Mei.
Afiliación
  • Lai ZZ; Graduate Institute of Medical Science, National Defense Medical Center, Taipei 114, Taiwan.
  • Yen IC; Department and Graduate Institute of Pharmacology, National Defense Medical Center, Taipei 114, Taiwan.
  • Hung HY; School of Pharmacy, National Defense Medical Center, Taipei 114, Taiwan.
  • Hong CY; Department and Graduate Institute of Pharmacology, National Defense Medical Center, Taipei 114, Taiwan.
  • Lai CW; Department and Graduate Institute of Pharmacology, National Defense Medical Center, Taipei 114, Taiwan.
  • Lee YM; School of Pharmacy, National Defense Medical Center, Taipei 114, Taiwan.
Pharmaceuticals (Basel) ; 17(8)2024 Jul 26.
Article en En | MEDLINE | ID: mdl-39204093
ABSTRACT
Zika virus (ZIKV) and Japanese encephalitis virus (JEV) can cause permanent neurological damage and death, yet no approved drugs exist for these infections. Rhodiola crenulate, an herb used in traditional Chinese medicine for its antioxidation and antifatigue properties, was studied for its antiviral activity against ZIKV and JEV in vitro. The cytotoxicity of Rhodiola crenulata extract (RCE) was evaluated using the CCK-8 reagent. Antiviral effects of RCE were assessed in ZIKV-infected or JEV-infected Vero cells via quantitative reverse transcription polymerase chain reaction (qRT-PCR), Western blotting, fluorescent focus assay (FFA), and immunofluorescence assay (IFA). The cell-free antiviral effects of RCE were evaluated using an inactivation assay. To determine the stage of the viral life cycle affected by RCE, time-of-addition, binding, and entry assays were conducted. Three bioactive constituents of RCE (salidroside, tyrosol, and gallic acid) were tested for antiviral activity. RCE exhibited dose-dependent anti-ZIKV and anti-JEV activities at non-cytotoxic concentrations, which were likely achieved by disrupting viral binding and stability. Gallic acid exhibited antiviral activity against ZIKV and JEV. Our findings indicate that RCE disrupts viral binding and stability, presenting a potential strategy to treat ZIKV and JEV infections.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pharmaceuticals (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Taiwán Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pharmaceuticals (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Taiwán Pais de publicación: Suiza