Antiviral Activity of Chrysin Derivatives against Coxsackievirus B3 in vitro and in vivo.
10.4062/biomolther.2015.095
- Author:
Jae Hyoung SONG
1
;
Bo Eun KWON
;
Hongjun JANG
;
Hyunju KANG
;
Sungchan CHO
;
Kwisung PARK
;
Hyun Jeong KO
;
Hyoungsu KIM
Author Information
1. Laboratory of Microbiology and Immunology, College of Pharmacy, Kangwon National University, Chuncheon 200-701, Republic of Korea. hjko@kangwon.ac.kr
- Publication Type:In Vitro ; Original Article
- Keywords:
Antiviral activity;
Coxsackievirus B3;
Chrysin;
Flavonoid;
Pancreatitis
- MeSH:
Acinar Cells;
Animals;
Enterovirus;
Inflammation;
Injections, Intraperitoneal;
Mice;
Myocarditis;
Pancreatitis;
Vero Cells
- From:Biomolecules & Therapeutics
2015;23(5):465-470
- CountryRepublic of Korea
- Language:English
-
Abstract:
Chrysin is a 5,7-dihydroxyflavone and was recently shown to potently inhibit enterovirus 71 (EV71) by suppressing viral 3C protease (3Cpro) activity. In the current study, we investigated whether chrysin also shows antiviral activity against coxsackievirus B3 (CVB3), which belongs to the same genus (Enterovirus) as EV71, and assessed its ability to prevent the resulting acute pancreatitis and myocarditis. We found that chrysin showed antiviral activity against CVB3 at 10 muM, but exhibited mild cellular cytotoxicity at 50 muM, prompting us to synthesize derivatives of chrysin to increase the antiviral activity and reduce its cytotoxicity. Among four 4-substituted benzyl derivatives derived from C(5) benzyl-protected derivatives 7, 9-11 had significant antiviral activity and showed the most potent activity against CVB3 with low cytotoxicity in Vero cells. Intraperitoneal injection of CVB3 in BALB/c mice with 1x106 TCID50 (50% tissue culture infective dose) of CVB3 induced acute pancreatitis with ablation of acinar cells and increased serum CXCL1 levels, whereas the daily administration of 9 for 5 days significantly alleviated the pancreatic inflammation and reduced the elevation in serum CXCL1 levels. Collectively, we assessed the anti-CVB3 activities of chrysin and its derivatives, and found that among 4-substituted benzyl derivatives, 9 exhibited the highest activity against CVB3 in vivo, and protected mice from CVB3-induced pancreatic damage, simultaneously lowering serum CXCL1 levels.
