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Aloe-emodin is an interferon-inducing agent with antiviral activity against Japanese encephalitis virus and enterovirus 71

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Author(s): Lin, CW (Lin, Cheng-Wen); Wu, CF (Wu, Chia-Fang); Hsiao, NW (Hsiao, Nai- Wan); Chang, CY (Chang, Ching-Yao); Li, SW (Li, Shih-Wein); Wan, L (Wan, Lei); Lin, YJ (Lin, Ying-Ju); Lin, WY (Lin, Wei-Yong)

Title: Aloe-emodin is an interferon-inducing agent with antiviral activity against Japanese encephalitis virus and enterovirus 71

Source: INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 32 (4): 355-359 OCT 2008

Language: English Document Type: Article

Author Keywords: aloe-emodin; interferon signalling; Japanese encephalitis virus;

enterovirus 71

KeyWords Plus: NITRIC-OXIDE; IN-VITRO; INFECTION; ANTHRAQUINONES;

DERIVATIVES; INHIBITION; ACTIVATION; MICE

Abstract: In this study, aloe-emodin was identified as a potential interferon (IFN)-inducer by screening compounds from Chinese herbal medicine. Aloe-emodin showed low cytotoxicity to human HL-CZ promonocyte cells and TE-671 medulloblastoma cells and significantly

activated interferon-stimulated response element (ISRE) and gamma-activated sequence (GAS)-driven cis-reporting systems. Moreover, aloe-emodin upregulated expression of IFN- stimulated genes such as dsRNA-activated protein kinase and 2', 5'-oligoisoadenylate

synthase. Aloe-emodin resulted in significant activation of nitric oxide production. The antiviral activity of aloe-emodin against Japanese encephalitis virus (JEV) and enterovirus 71 (EV71) was evaluated using dose- and time-dependent plaque reduction assays in HL-CZ cells and TE-671 cells. The 50% inhibitory concentration (IC50) of aloe-emodin ranged from 0.50 mu g/mL to 1.51 mu g/mL for JEV and from 0.14 mu g/mL to 0.52 mu g/mL for EV71. Aloe-emodin showed clearly potent virus inhibitory abilities and achieved high therapeutic indices, in particular for HL-CZ cells. Therefore, the study demonstrated dose- and time-dependent actions of aloe-emodin on the inhibition of JEV and EV71 replication via IFN signalling responses. (C) 2008 Elsevier B. V. and the International Society of Chemotherapy. All rights reserved.

Addresses: [Lin, Cheng-Wen; Li, Shih-Wein] China Med Univ, Dept Med Lab Sci &

Biotechnol, Taichung 404, Taiwan; [Wu, Chia-Fang] China Med Univ, Dept Lab Med, Clin Virol Lab, Taichung 404, Taiwan; [Lin, Cheng-Wen; Wu, Chia-Fang; Chang, Ching-Yao] Asia Univ, Dept Biotechnol & Bioinformat, Taichung 413, Taiwan; [Wu, Chia-Fang] China Med Univ Hosp, Ctr Mol Med, Taichung 404, Taiwan; [Hsiao, Nai-Wan] Natl Changhua Univ Educ, Inst Biotechnol, Changhua 500, Taiwan; [Wan, Lei; Lin, Ying-Ju; Lin, Wei-Yong] China Med Univ, Dept Med Genet & Med Res, Taichung 404, Taiwan

Reprint Address: Lin, CW, China Med Univ, Dept Med Lab Sci & Biotechnol, 91 Hsueh Shih

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Rd, Taichung 404, Taiwan.

E-mail Address: [email protected] Funding Acknowledgement:

Funding Agency Grant Number

National Science Council of R. O. C. (Taiwan) NSC95-2745-B-039-003-URD

China Medical University CMU95-054

National Science Council of R. O. C. (Taiwan) (NSC95-2745-B-039-003-URD); and China Medical University (CMU95-054).

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BURKE DS, 2001, FIELDS VIROLOGY, P1043.

CHANG EE, 2007, J HAZARD MATER, V146, P356, DOI 10.1016/j.jhazmat.2006.12.035.

CHEN X, 2002, PHYTOTHER RES, V16, P199.

HENG C, 2007, VIRUS RES, V127, P88, DOI 10.1016/j.virusres.2007.03.022.

KEYAERTS E, 2004, INT J INFECT DIS, V8, P223, DOI 10.1016/j.ijid.2004.04.012.

LEWIS M, 2007, PHARMACOTHERAPY, V27, P455.

LIN YL, 1997, J VIROL, V71, P5227.

LIU ML, 2005, J GEN VIROL 12, V86, P3263, DOI 10.1099/vir.0.81195-0.

MCMINN PC, 2002, FEMS MICROBIOL REV, V26, P91.

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Cited Reference Count: 14 Times Cited: 3

Publisher: ELSEVIER SCIENCE BV

Publisher Address: PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS ISSN: 0924-8579

DOI: 10.1016/j.ijantimicag.2008.04.018

29-char Source Abbrev.: INT J ANTIMICROBIAL AGENTS ISO Source Abbrev.: Int. J. Antimicrob. Agents

Source Item Page Count: 5

Subject Category: Infectious Diseases; Microbiology; Pharmacology & Pharmacy ISI Document Delivery No.: 345JJ

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