Efficacy of Brazilian Propolis against Herpes Simplex Virus Type 1 Infection in Mice and Their Modes of Antiherpetic Efficacies

Author:

Shimizu Tomomi1,Takeshita Youhei1,Takamori Yasushi1,Kai Hisahiro2,Sawamura Rie1,Yoshida Hiroki1,Watanabe Wataru3,Tsutsumi Atsuko4,Park Yong Kun5,Yasukawa Ken6,Matsuno Koji2,Shiraki Kimiyasu7,Kurokawa Masahiko1

Affiliation:

1. Department of Biochemistry, School of Pharmaceutical Sciences, Kyushu University of Health and Welfare, 1714-1 Yoshino, Nobeoka, Miyazaki 882-8508, Japan

2. Department of Pharmaceutical Health Sciences, School of Pharmaceutical Sciences, Kyushu University of Health and Welfare, 1714-1 Yoshino, Nobeoka, Miyazaki 882-8508, Japan

3. Department of Microbiology, School of Pharmaceutical Sciences, Kyushu University of Health and Welfare, 1714-1 Yoshino, Nobeoka, Miyazaki 882-8508, Japan

4. Amazonfood Ltd., 2-24-28 Ohhara, Setagaya, Tokyo 156-0041, Japan

5. Department of Food Science, College of Food Engineering, State University of Campinas, P.O. Box 6177, 13083-970 Campinas, SP, Brazil

6. School of Pharmacy, Nihon University, 7-7-1 Narashinodai, Funabashi-shi, Chiba 274-8555, Japan

7. Department of Virology, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan

Abstract

Ethanol extracts (AF-06, 07, and 08, 10 mg/kg) of Brazilian propolis were administered orally to cutaneously herpes simplex virus type 1 (HSV-1)-infected mice three times daily on days 0 to 6 after infection to evaluate their efficacies against HSV-1 infection and significantly limited development of herpetic skin lesions. AF-07 and 08 significantly reduced virus titers in brain and/or skin on day 4 without toxicity, but AF-08 had no anti-HSV-1 activityin vitro. AF-06 and 08 significantly enhanced delayed-type hypersensitivity (DTH) to inactivated HSV-1 antigen in infected mice. Oral AF-08-administration significantly augmented interferon (IFN)-γproduction by HSV-1 antigen from splenocytes of HSV-1-infected mice, while direct exposure of splenocytes of infected mice to AF-06 significantly elevated IFN-γproductionin vitro. Thus, AF-08 might have components that are activein vivoeven after oral administration and those of AF-06 might be active onlyin vitro. Because DTH is a major host defense for intradermal HSV-1 infection, augmentation of DTH response by AF-06 or 08, directly or indirectly, respectively, may contribute to their efficacies against HSV-1 infection. In addition, AF-06 and 07 possibly contain anti-HSV-1 components contributing to their efficacies. Such biological activities of Brazilian propolis may be useful to analyze its pharmacological actions.

Funder

Japan Society for the Promotion of Science

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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