Macrophage-mediated inhibitory effect of Zingiber officinale Rosc, a traditional Oriental herbal medicine, on the growth of influenza A/Aichi/2/68 virus

American Journal of Chinese Medicine

Volumn 34, Issue 1, 2006, Pages 157-169

  Imanishi, Nobuko ^a   Andoh, Tsugunobu ^a   Mantani, Naoki ^c   Sakai, Shinya ^a   Terasawa, Katsutoshi ^a,b   Shimada, Yutaka ^a,b   Sato, Miyuki ^a   Katada, Yuko ^a   Ueda, Kyouka ^a   Ochiai, Hiroshi ^a,b  

^a UNIVERSITY OF TOYAMA   (Japan)

^b TOYAMA MEDICAL AND PHARMACEUTICAL UNIVERSITY   (Japan)

^c GUNMA UNIVERSITY   (Japan)

Author keywords

Influenza virus; Macrophages; TNF ; Zingiber officinale Rosc

Indexed keywords

GINGER EXTRACT; MESSENGER RNA; TUMOR NECROSIS FACTOR ALPHA; TUMOR NECROSIS FACTOR ALPHA ANTIBODY;

ANIMAL CELL; ANTIGEN ANTIBODY COMPLEX; ANTIVIRAL ACTIVITY; ARTICLE; CELL CULTURE; CONCENTRATION (PARAMETERS); CONCENTRATION RESPONSE; CONTROLLED STUDY; CYTOKINE PRODUCTION; CYTOTOXICITY; DOG; DRUG MECHANISM; ENZYME LINKED IMMUNOSORBENT ASSAY; GENE EXPRESSION; HERBAL MEDICINE; INFLUENZA VIRUS A; KIDNEY CELL; MACROPHAGE ACTIVATION; MACROPHAGE FUNCTION; MOUSE; NONHUMAN; ORIENTAL MEDICINE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; STATISTICAL ANALYSIS; STATISTICAL SIGNIFICANCE; VIROGENESIS;

ANIMALS; ANTIBODIES, MONOCLONAL; CELL LINE; DOGS; DOSE-RESPONSE RELATIONSHIP, DRUG; DRUGS, CHINESE HERBAL; GINGER; INFLUENZA A VIRUS, H3N2 SUBTYPE; LIPOPOLYSACCHARIDES; MACROPHAGES; MICE; RNA, MESSENGER; TIME FACTORS; TUMOR NECROSIS FACTOR-ALPHA;

EID: 32544435791     PISSN: 0192415X     EISSN: None     Source Type: Journal    
DOI: 10.1142/S0192415X06003722     Document Type: Article

References (40)

1. Abbas, A.K., A.H. Lichtman and J.K. Pober. Cellular and Molecular Immunology, 4th ed. W. B. Saunders Company, Philadelphia, PA, 1991, pp. 235-269.
2. Aggarwal, B.B., J. Vilcek (eds.) Tumor Necrosis Factor: Structure, Function and Mechanism of Action. Marcel Dekker Inc., New York, NY, 1991, pp. 235-269.
3. Campen, H.V. Influenza A virus replication is inhibited by tumor necrosis factor-α in vitro. Arch. Virol. 136: 439-446, 1994.
4. Carswell, E.A., L.J. Old, R.L. Kassel, S. Green, N. Fiore and B. Williamson. An endotoxin-induced serum factor that causes necrosis of tumors. Proc. Natl. Acad. Sci. USA 72: 3666-3670, 1975.
5. Chomczynski, P. and N. Sacchi. Single-step method of RNA isolation by acid guanidinium thiocyanatephenol-chloroform extraction. Anal. Biochem. 162: 156-159, 1987.
6. Conn, C.A., J.L. McClellan, H.F. Maassab, C.W. Smitka, J.A. Majde and M.J Kluger. Cytokines and the acute-phase response to influenza virus in mice. Am. J. Physiol. 268: R78-84, 1995.
7. Fort, P., L. Marty, M. Piechaczyk, S. el Sabrouty, C. Dani, P. Jeanteur and J.M. Blanchard. Various rat adult tissues express only one major mRNA species from the glyceraldehyde-3-phosphate-dehydrogenase multigenic family. Nucleic Acids Res. 13: 1431-1442, 1985.
8. Grace, H.W.W., F.K. John, P.S. Daniel and V.G. David. In vitro anti-human immunodeficiency virus activities of tumor necrosis factor-α and interferon-γ. J. Immunol. 140: 120-124, 1988.
9. Hofmann, P., H. Sprenger, A. Kaufmann, A. Bender, C. Hasse, M. Nain and D. Gemsa. Susceptibility of mononuclear phagocytes to influenza A virus infection and possible role in the antiviral response. J. Leukocyte Biol. 61: 408-414, 1997.
10. Houde, M. and D.J. Arora. Stimulation of tumor necrosis factor secretion by purified influenza virus neuraminidase. Cell. Immunol. 129: 104-111, 1990.
11. Imanishi, N., N. Mantani, T. Andoh, S. Sakai, K. Ueda, K. Terasawa and H. Ochiai. Inhibitory effect of Zingiber officinale Rosc, an Oriental medicine, on the growth of influenza A/Aichi/2/68 virus in MDCK cells via macrophage activation. Microbiol. Immunol. 49: 41-48, 2005.
12. Imanishi, N., Y. Tuji, Y. Katata, M. Maruhashi, S. Konosu, N. Mantani, K. Terasawa and H. Ochiai. Additional inhibitory effect of tea extract on the growth of influenza A and B viruses in MDCK cells. Microbiol. Immunol. 47: 491-494, 2002.
13. Ito, M. and J.A. O'Malley. Antiviral effect of recombinant human tumor necrosis factor. Lymphokine Res. 6: 309-318, 1987.
14. Jakeman, K.J., C.R. Bird, R. Thorpe, H. Smith and C. Sweet. Nature of the endogenous pyrogen (EP) induced by influenza viruses: Lack of correlation between EP levels and content of the known pyrogenic cytokines, interleukin 1, interleukin 6 and tumor necrosis factor. J. Gen. Virol. 72: 705-709, 1991.
15. Kaiser, L., R.S. Fritz, S.E. Straus, L. Gubareva and F.G. Hayden. Symptom pathogenesis during acute influenza: Interleukin-6 and other cytokine responses. J. Med. Virol. 64: 262-268, 2001.
16. Kallas, E.G., R.J. Andrews, J.J. Treanor and T.G. Evans. Production of influenza-stimulated tumor necrosis factor-α by monocytes following acute influenza infection in humans. J. Interf. Cyto. Res. 19: 751-755, 1999.
17. Kawamata, H., H. Ochiai, N. Mantani and K. Terasawa. Enhanced expression of inducible nitric oxide synthase by Juzen-taiho-to in LPS-activated RAW264.7 cells, a murine macrophage cell line. Am. J. Chin. Med. 28: 217-226, 2000.
18. Keith, R.W., E.M. Treena, H. Yugi and H. Shizu. Modulation of proinflammatory Cyokines by nitric oxide in murine acute lung injury. Am. J. Respir. Crit. Care Med. 160: 698-704, 1999.
19. Khaiboullina, S.F., D.M. Netski, P. Krumpe and S.C. St. Jeor. Effects of tumor necrosis factor alpha on sin nombre virus infection in vivo. J. Virol. 74: 11966-11971, 2000.
20. Lane, B.R., D.M. Markovitz, N.L. Woodford, R. Rochford, R.M. Strieter and M.J. Coffey. TNF-inhibits HIV-1 replication in peripheral blood monocytes and alveolar macrophages by inducing the production of RANTES and decreasing C-C chemokine receptor 5 expression. J. Immunol. 163: 3653-3661, 1999.
21. Lehmann, C., H.M. Sprenger, M. Nain, M. Bacher and D. Gemsa. Infection of macrophages by influenza A virus: Characteristics of tumour necrosis factor-α (TNFα) gene expression. Res. Virol. 147: 123-130, 1996.
22. Lyons, C.R., G.J. Orloff and J.M. Cunningham. Molecular cloning and functional expression of an inducible nitric oxide synthase from a murine macrophage cell line. J. Biol. Chem. 267: 6370-6374, 1992.
23. Mantani, N., T. Andoh, H. Kawamata, K. Terasawa and H. Ochiai. Inhibitory effect of Ephedrae herba, an Oriental traditional medicine, on the growth of influenza A/PR/8 virus in MDCK cells. Antiviral Res. 44: 193-200, 1999.
24. Mantani, N., N. Imanishi, H. Kawamata, K. Terasawa and H. Ochiai. Inhibitory effect of (+)-catechin on the growth of influenza A/PR/8 virus in MDCK cells. Planta Med. 67: 240-224, 2001.
25. Mestan, J., W. Digel, S. Mittnacht, H. Hillen, D. Blohm, A. Moller, H. Jacobsen and H. Kirchner. Antiviral effects of recombinant tumor necrosis factor in vitro. Nature 323: 816-819, 1986.
26. Mock, D.J., F. Domurat, N.J. Roberts, E.E. Walsh Jr, M.R. Licht and P. Keng. Macrophages are required for influenza virus infection of human lymphocytes. J. Clin. Invest. 78: 620-624, 1987.
27. Mosmann, T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 65: 55-63, 1983.
28. Nagai, T., M. Ureta and H. Yamada. In vivo anti-influenza virus activity of Kampo (Japanese herbal) medicine "sho-seiryu-to"-effects on aged mice, against subtypes of A viruses and B virus, and therapeutic effect. Immunopharmacol. Immunotoxicol. 18: 193-208, 1997.
29. Nagai, T. and H. Yamada. In vivo anti-influenza virus activity of Kampo (Japanese herbal) medicine "Sho-seiryu-to" and its mode of action. Int. J. Immunopharmacol. 16: 605-613, 1994.
30. Nain, M., F. Hinder, J.H. Gong, A. Schmidt, A. Bender, H. Sprenger and D. Gemsa. Tumor necrosis factor-α production of influenza A virus infected macrophages and potentiating effect of lipopolysaccharides. J. Immunol. 145: 1921-1928, 1990.
31. Ochiai, H., A. Ikesue, M. Kurokawa, K. Nakajima and H. Nakagawa. Enhanced production of rat interleukin-8 by in vitro and in vivo infections with influenza A NWS virus. J. Virol. 67: 6811-6814, 1993.
32. Peschke, T., A. Bender, M. Nain and D. Gemsa. Role of macrophage cytokines in influenza A virus infection. Immunobiology 189: 340-355, 1993.
33. Rossol-Voth, R., S. Rossol, K.H. Schutt, S. Corridori, W. de Cian and D. Falke. In vivo protective effect of tumor necrosis factor-α against experimental infection with herpes simplex virus type 1. J. Gen. Virol. 72: 143-147, 1991.
34. Seo, S.H. and R.G. Webster. Tumor necrosis factor alpha exerts powerful ani-influenza virus effects in lung epithelial cells. J. Virol. 76: 1071-1076, 2002.
35. Sprenger, H., M. Bacher, E. Rischkowsky, A. Bender, M. Nain and D. Gemsa. Characterization of high molecular weight tumor necrosis factor-α mRNA in influenza A virus-infected macrophages. J. Immunol. 152: 280-289, 1994.
36. Takasuka, N., T. Tokunaga and K.S. Akagawa. Pre-exposure of macrophages to low doses of lipopolysaccharide inhibits the expression of tumor necrosis factor-α mRNA but not of IL-β mRNA. J. Immunol 146: 3824-3830, 1991.
37. Terada, Y., K. Tomita, H. Nonoguchi, T. Yang and F. Marumo. Different localization and regulation of two types of vasopressin receptor messenger RNA in microdissected rat nephron segments using reverse transcription polymerase chain reaction. J. Clin. Invest. 92: 2339-2345, 1993.
38. Thierry, H., J.Z. Hermann, F. Karl and P.A. Ernst. kinetic study of immune mediators in the lung of mice infected with influenza A virus. J. Immunol. 149: 932-939, 1992.
39. Tobita, K. Permanent canine kidney (MDCK) cells for isolation and plaque assay of influenza B virus. Med. Microbiol. Immunol. 62: 23-27, 1975.
40. Wyde, P.R., D.J. Peavy and T.R. Cate. Morphological and cytochemical characterization of cells infiltrating mouse lungs after influenza infection. Infect. Immun. 21: 140-146, 1978.