Research Article
Protective effect of brown Brazilian propolis against acute vaginal lesions caused by herpes simplex virus type 2 in mice: involvement of antioxidant and anti-inflammatory mechanisms
Article first published online: 24 OCT 2011
DOI: 10.1002/cbf.1810
Copyright © 2011 John Wiley & Sons, Ltd.
Additional Information
How to Cite
Sartori, G., Pesarico, A. P., Pinton, S., Dobrachinski, F., Roman, S. S., Pauletto, F., Rodrigues, L. C. and Prigol, M. (2012), Protective effect of brown Brazilian propolis against acute vaginal lesions caused by herpes simplex virus type 2 in mice: involvement of antioxidant and anti-inflammatory mechanisms. Cell Biochem. Funct., 30: 1–10. doi: 10.1002/cbf.1810
Publication History
- Issue published online: 3 JAN 2012
- Article first published online: 24 OCT 2011
- Manuscript Accepted: 24 AUG 2011
- Manuscript Revised: 25 JUL 2011
- Manuscript Received: 18 MAY 2011
Funded by
- FAPERGS
- CAPES
- CNPq
- Abstract
- Article
- References
- Cited By
Keywords:
- HSV-2;
- herpes;
- propolis;
- antioxidant;
- anti-inflammatory
Propolis has been highlighted for its antioxidant, anti-inflammatory and antiviral properties. The purpose of this study was to investigate if brown Brazilian hydroalcoholic propolis extract (HPE) protects against vaginal lesions caused by herpes simplex virus type 2 (HSV-2) in female BALB/c mice. The treatment was divided in 5 days of pre-treatment with HPE [50 mg·kg–1, once a day, intragastric (i.g.)], HSV-2 infection [10 µl of a solution 1 × 102 plaque-forming unit (PFU·ml–1 HSV-2), intravaginal inoculation at day 6] and post-treatment with HPE (50 mg·kg–1) for 5 days more. At day 11, the animals were killed, and the in vivo analysis (score of lesions) and ex vivo analysis [haematological and histological evaluation; superoxide dismutase (SOD), catalase (CAT) and myeloperoxidase (MPO) activities; reactive species (RS), tyrosine nitration levels, non-protein thiols (NPSH) and ascorbic acid (AA) levels] were carried out. HPE treatment reduced extravaginal lesions and the histological damage caused by HSV-2 infection in vaginal tissues of animals. HPE was able to decrease RS, tyrosine nitration, AA levels and MPO activity. Also, it protected against the inhibition of CAT activity in vaginal tissues of mice. HPE promoted protective effect on HSV-2 infected animals by acting on inflammatory and oxidative processes, and this effect probably is caused by its antioxidant and anti-inflammatory properties. Copyright © 2011 John Wiley & Sons, Ltd.

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