14
Views
5
CrossRef citations to date
0
Altmetric
Research Article

Stimulatory Action of Plucheu quitoc Extract on the Hematopoietic Response During Murine Listeriosis

, , , &
Pages 721-740 | Published online: 27 Sep 2008

References

  • Martino V. S., Ferraro G. E., Coussio J. D. Flavonoids from Argentine medicinal plants. Part 10. New flavonoid from Pluchea sagittalis. Phytochemistry 1976; 15: 1086
  • Martino V. S., Debenedetti S. L., Coussio J. D. Caffeoylquinic acids from Pterocaulon virgatum and Pluchea sagittalis. Phytochemistry 1979; 18: 2052
  • Rodriguez E., Wrangham R. Phytochemical potential of tropical plants, K. R. Downum. Plenum Press, New York 1993
  • Scholz E., Heinrich M., Hunkler D. Caffeoylquinic acids and some biological activities of Pluchea symphytifolia. Planta Medica 1994; 60: 360
  • Maia J. G.S., Silva M. H.L. Potencial econěmico de plantas aromaticas do Pará. Museu Paraense Emílio Goeldi, Belém, PA 1995
  • Martino V. S., Ferraro G. E., Debenedetti S. L., Coussio J. D. Compuestos polifenolicos aislados de Pluchea sagittalis (Compuestas). Acta Farm. Bonaerense 1984; 3: 141
  • Ushiyama T., Miyase T., Ueno A., Usmanghani K. Terpenic glycosides from Pluchea indica. Phytochemistry 1989; 28: 3369
  • Chawla A. S., Kaith B. S., Handa S. S., Kulshreshta K. D., Srimal R. C. Chemical investigation and antiinflammatory activity of Pluchea lanceolata roots. Indian J. Chem. Section B 1990; 29B: 918
  • Guilhon G. M.S.P., Muller A. H. Eudesmane derivatives from Pluchea quitoc. Phytochemistry 1996; 43: 417
  • Guilhon G. M.S.P., Muller A H. Eudesmane sesquiterpenoids from Pluchea quitoc. Phytochemistry 1998; 47: 227
  • Guilhon G. M.S.P., Müller A. H. Eudesmanolides and epoxycuauthemones from Pluchea quitoc. Phytochemistry 1998; 49: 1347
  • Guilhon G. M.S.P. Investigação fitoquímica de Pluchea quitoc com contribuiçãgo à quimica do gěero Pluchea (Asteraceae). Universidade Federal Rural do Rio de Janeiro, Rio de Janeiro 2000, Ph.D. Tesis
  • Gorzalczany S., Acevedo C., Muschietti L., Martino V., Ferraro G. Search for antiinflammatory activity in Argentine medicinal plants. Phytomedicine 1996; 3: 181
  • Wagner H. Search for plant derived natural products with immunostimulatory activity (recent advances). Pure Appl. Chem. 1990; 62: 1217
  • Sen T., Chaudhuri A. K.N. Antiinflammatory evaluation of a Pluchea indica root extract. J. Ethnopharmacol. 1991; 33: 135
  • Sen T., Ghosh T. K., Chaudhuri A. K.N. Studies on the mechanism of antiinflammatory and antiulcer activity of Pluchea indica- Probable involvement of 5-lipooxygenase pathway. Life Sci. 1993; 52: 737
  • Locher C. P., Witvrouw M., deBethune M. P., Burch M. T., Mower H. F., Davies H., Lasure A., Pauwels R., deClercq E., Vlietinck A. J. Antiviral activity of Hawaiian medicinal plants against human immunodeficiency virus type-1 (HIV-1). Phytomedicine 1996; 2: 259
  • Pérez-Garcia F., Marin E., Canigueral S., Adzet T. Anti-inflammatory action of Pluchea sagittalis: Involvement of an antioxidant mechanism. Life Sci. 1996; 59: 2033
  • Perez F., Marin E., Adzet T. The antiinflammatory effect of several compositae from South-America extracts in rats. Phytother. Res. 1995; 9: 145
  • Tatefuji T., Izumi N., Ohta T., Arai S., Ikeda M., Kurimoto M. Isolation and identification of compounds from Brazilian propolis which enhance macrophage spreading and mobility. Biol. Pharm. Bull. 1996; 19: 966
  • Jones D. Foodborne listeriosis. Lancet 1990; 336: 1171
  • Schuchat A., Deaver K. A., Wenger J. D., Plikaytis B. D., Mascola L., Pinner R. W., Reingold A. L., Broome C. V. Role of foods in sporadic listeriosis. I. Case-control study of dietary risk factors. JAMA 1992; 267: 2041
  • Mackaness G. B. Cellular resistance to infection. J. Exp. Med. 1962; 116: 381
  • Kaufmann S. H.E. Immunity to intracellular microbial patogens. Immunol. Today 1995; 16: 338
  • North R. J., Conlan J. W. Immunity to Listeria monocytogenes. Chem. Immunol. 1998; 70: 1
  • Wing E. J., Barczynski L. K., Waheed A., Shadduck R. K. Effect of Listeria monocytogeries infection on serum levels of colony-stimulating factor and number of progenitor cells in immune and non-immune animals. Infect. Immun. 1985; 49: 325
  • Bancroft G. J., Schreiber R. D., Unanue E. R. Natural immunity: A T-cell independent pathway of macrophage activation defined in the SCID mouse. Immunol. Rev. 1991; 124: 5
  • North R. J. The relative importance of blood monocytes and fixed macrophages to the expression of cell-mediated immunity to infection. J. Exp. Med. 1970; 132: 521
  • Kaufmann S. H.E. Immunity to intracellular bacteria. Ann. Rev. Immunol. 1993; 11: 129
  • Czuprynski C. J., Brown J. F., Marousheck N., Wagner R. D., Steinberg H. Neutrophil depletion by administration of anti-granulocyte mAb RB6–8C5 impairs the resistance of mice to Listeria monocytogenes infection. J. Immunol. 1994; 152: 1836
  • Czuprynski C. J., Haak-Frendscho M. Non-specific resistance mechanisms to listeriosis: Implications for experimental and naturally ocurring infection. Immunol. Rev. 1997; 158: 47
  • Metcalf D. The colony-stimulating factors: Discovery to clinical use. Phil. Trans. R. Soc. Lond. 1991; 333: 147
  • Wing E. J., Waheed A., Shadduck R. K. Changes in serum colony-stimulating factor and monocytic progenitor cells during Listeria monocytogenes infection in mice. Infect. Immun. 1984; 45: 180
  • Cheers C., Stanley E. R. Macrophage production during murine listeriosis: Colony-stimulating factor 1 (CSF-1) and CSF-1-binding cells in genetically resistant and susceptible mice. Infect. Immun. 1988; 56: 2972
  • Gregory S. H., Magee D. M., Wing E. J. The role of colony-stimulating factors in host defenses. Proc. Soc. Exp. Biol. Med. 1991; 197: 349
  • Cheers C., Haigh A. M., Kelso A., Metcalf D., Stanley E. R., Young A. M. Production of colony-stimulating factors (CSFs) during infection: Separate determinations of macrophage-, granulocyte-. granulocyte-macrophage-, and multi-CSFs, Infect. Immun. 1988; 56: 247
  • Young A. M., Cheers C. Colony-forming cells and colony-stimulating activity during listeriosis in genetically resistant or susceptible mice. Cell. Immunol. 1986; 97: 227
  • Wing E. J., Barczynski L. K., Sherbondy J. M. Effect of acute nutritional deprivation on macrophage colony-stimulating factor and macrophage progenitor cells in mice. Infect. Immun. 1986; 54: 245
  • Bincoletto C., Queiroz M. L.S. The effect of lead on the bone marrow stem cells of mice infected with Listeria monocytogenes. Vet. Human Toxicol. 1996; 38: 186
  • Quadros M. R., Souza-Brito A. R.M., Queiroz M. L.S. Petiveria alliacea L. extract protects mice against Listeria monocytogenes infection-Effects on bone marrow progenitor cells. Immunopharmacol. Immunotoxicol. 1999; 21: 109
  • Dantas D. C.M., Queiroz M. L.S. Effects of Chlorella vulgaris on bone marrow progenitor cells of mice infected with Listeria monocytogenes. Int. J. Immunopharmacol. 1999; 21: 499
  • Dantas D. C.M., Kaneno R., Queiroz M. L.S. The effect of Chlorella vulgaris in the protection of mice infected with Listeria monocytogenes. Role of natural killer cells, Immunopharmacol. Immunotoxicol. 1999; 21: 609
  • Queiroz M. L.S., Quadros M. R., Santos L. M.B. Cytokine profile and natural killer cell activity in Listeria monocytogenes infected mice treated orally with Petiveria alliacea extracts. Immunopharmacol. Immunotoxicol., submitted
  • Melo A., Justo G. Z., Queiroz M. L.S. Recovery of myelopoiesis and increased resistance to Listeria monocytogenes in mice treated with an aggregated polymer isolated fiom Aspergillus oryzae. Int. J, Immunopharmacol., submitted
  • Levin J., Bang F. B. Clottable protein Limulus: Its localization and kinetics of its coagulation by endotoxin. Thromb. Diath. Haemorrh. 1968; 19: 186
  • Metcalf D. The hematopoietic colony stimulating factors. Elsevier, Amsterdam 1984
  • Gervais A., Morris-Hooke A., Tran T. A., Skamene E. Analysis of macrophage bacterial function in genetically resistant and susceptible mice using the temperature-sensitive mutant of Listeria monocytogenes. Infect. Immun. 1986; 54: 315
  • Queiroz M. L.S., Justo G. Z., Silva M. R. Effects of the green algae Chlorella vulgaris on the response of the host hematopoietic system to intraperitoneal Ehrlich ascites tumor transplantation in mice. Int. J. Immunopharmacol., submitted
  • Mielke M. E.A., Ehlers S., Hahn H. T-cell subsets in delayed-type hypersensitivity, protection and granuloma formation in primary and secondary Listeria infection in mice: Superior role of Lyt-2+ cells in acquired immunity. Infect. Immun. 1988; 56: 1920
  • Czuprynski C. J., Henson P. M., Campbell P. A. Enhanced accumulation of inflammatory neutrophils and macrophage mediated by transfer of T cells fiom mice immunized with Listeria monocytogenes. J. Immunol. 1985; 134: 3449
  • Czuprynski C. J., Brown J. F. The relative difference in antilisterial resistance of C57B1/6 and A/J mice is not eliminated by active immunization or by transfer of Listeria-immune T cells. Immunol. 1986; 58: 437
  • Mandel T. E., Cheers C. Resistance and susceptibility of mice to bacterial infection: histopathology of listeriosis in resistant and susceptible strains. Infect. Immun. 1980; 30: 851
  • Sadarangani C., Skamene E., Kongshavn P. A.L. Cellular basis for genetically determined enhanced resistance of certain mouse strains to listeriosis. Infect. Immun. 1980; 28: 381
  • Stevenson M. M., Kongshavn P. A.L., Skamene E. Genetic linkage of resistance to Listeria monocytogenes with macrophage inflammatory response. J. Immunol. 1981; 127: 402
  • Wood P. R., Spanidis V., Frangos K., Cheers C. The in vitro bactericidal activity of peritoneal and spleen cells from Listeria-resistant and susceptible mouse strains. Cell. Immunol. 1986; 99: 160
  • Lieschke G. J., Grail D., Hodgson G., Metcalf D., Stanley E., Cheers C., Fowler K. J., Basu S., Zhan Y. F., Dunn A. R. Mice lacking granulocyte stimulating factor have chronic neutropenia, granulocyte and macrophage progenitor cell. deficiency and impaired neutrophil mobilization. Blood 1994; 84: 1737
  • Zhan Y. F., Lieschke G. J., Grail D., Dunn A. R., Cheers C. Essential roles for granulocyte-macrophage colony-stimulating factor (GM-CSF) and G-CSF in sustained hematopoietic response of Listeria monocylogenes-infected mice. Blood 1998; 91: 863

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.