32
Views
13
CrossRef citations to date
0
Altmetric
Research Article

EVALUATION OF CAESALPINIA FERREA EXTRACT ON BONE MARROW HEMATOPOIESIS IN THE MURINE MODELS OF LISTERIOSIS AND EHRLICH ASCITES TUMOR

, , &
Pages 367-382 | Published online: 31 Jul 2001

REFERENCES

  • Hahn H., Kaufmann S. H.E. The role of cell-mediated immunity in bacterial infections. Rev. Infect. Dis. 1981; 3: 1221
  • Nathan C. F., Murray H. W., Wiebe M. E., Rubin B. Y. Identification of interferon-γ as the lymphokine that activates human macrophage oxidative metabolism and antimicrobial activity. J. Exp. Med. 1983; 158: 670
  • Werb Z. Basic and Clinical Immunology, D. P. Stiter, J. D. Stobo, J. V. Wells. 6th ed., Appleton and Lange, Norwalk 1987; 96
  • Cianciolo G. J. Inflammation: Basic Principles and Clinical Correlates, J. I. Gallin, I. M. Goldstein, R. Snyderman. Raven Press, New York 1988; 861
  • Murray H. W., Cohn Z. A. Mononuclear phagocyte antimicrobial and antitumor activity: the role of oxygen intermediates. J. Invest. Dermatol. 1980; 74: 285
  • Spector W. G., Ryan G. B. Mononuclear Phagocytes. Blackwell, Oxford 1970; 219
  • Fecchio D., Russo M., Sirois P., Braquet P., Jancar S. Inhibition of Ehrlich ascites tumor in vivo by PAF-antagonists. Int. J. Immunopharmacol. 1990; 12: 57
  • Fecchio D., Sirois P., Russo M., Jancar S. Studies on inflammatory response induced by Ehrlich tumour in mice peritoneal cavity. Inflammation 1990; 14: 125
  • Nelson J. A.S., Parhar R. S., Scodras J. M., Lala P. K. Down-regulation of macrophage I-A expression in tumor-bearing mice. J. Leukocyte Biol. 1990; 48: 394
  • Watson G. A., Lopez D. M. Aberrant antigen presentation by macrophages from tumour-bearing mice is involved in the down-regulation of their T-cell responses. J. Immunol. 1995; 155: 3124
  • Bonta I. L., Ben-Efraim S. Involvement of inflammatory mediators in macrophage antitumour activity. J. Leukocyte Biol. 1993; 54: 613
  • Barth M. W., Morahan P. S. Role of macrophages in the host response to Lewis lung peritoneal carcinomatosis. Cancer Immunol. Immunother. 1994; 38: 233
  • Fujiwara H., Hamaoka T. Regulatory mechanisms of antitumor T cell responses in the tumor-bearing state. Immunol. Res. 1995; 14: 271–291
  • Rocha M., Umansky V., Lee K.-H., Hacker H.-J., Benner A., Schirrmacher V. Differences between graft-versus-leukemia and graft-versus-host reactivity. I. Interaction of donor immune T cells with tumor and/or host cells. Blood 1997; 89: 2189
  • Elgert K. D., Alleva D. G., Mullins D. W. Tumour-induced immune dysfunction: the macrophage connection. J. Leukocyte Biol. 1998; 64: 275
  • Baum M., Fisher B. Macrophage production by the bone marrow of tumor bearing mice. Cancer Res. 1972; 32: 2813
  • Otu A. A., Russel R. J., Wilkinson P. C., White R. G. Alterations of mononuclear phagocyte function induces by Lewis lung carcinoma in C57BL mice. Br. J. Cancer 1977; 36: 330
  • Rhodes J. Resistance of tumor cells to macrophages: a short review. Cancer Immunol. Immunother. 1980; 7: 211–215
  • Roy M. R., Guhathakurta S., Roychowdhury J. Hematological changes in experimental tumours. Ind. J. Med. Res. 1981; 74: 896
  • Hardy C. L., Balducci L. Review: Hemopoietic alterations in cancer. Am. J. Med. Sci. 1985; 290: 196
  • Gabrilovich D., Ishida T., Oyama T., Ran S., Kravtsov V., Nadaf S., Carbone D. P. Vascular endothelial growth factor inhibits the development of dendritic cells and dramatically affects the differentiation of multiple hematopoietic lineages in vivo. Blood 1998; 92: 4150
  • Kusmartsev S., Ruiz de Morales J. M.G., Rullas J., Danilets M. G., Subiza J. L. Sialoadhesin expression by bone marrow macrophages derived from Ehrlich tumor-bearing mice. Cancer Immunol. Immunother. 1999; 48: 493
  • Parhar R. S., Lala P. K. Prostaglandin E2-mediated inactivation of various killer lineage cells by tumour-bearing host macrophages. J. Leukocyte Biol. 1988; 44: 185
  • Ruiz de Morales J., Velez D., Subiza J. L. Ehrlich tumor stimulates extramedullar hematopoiesis in mice without secreting identifiable colony-stimulating factors and without engagement of host T cells. Exp. Hematol. 1999; 27: 1757
  • Segura J. A., Barbero L. G., Márquez J. Early tumour effect on splenic Th lymphocytes in mice. FEBS Lett. 1997; 414: 1
  • Subiza J. L., Viñuela J. E., Rodriguez R., Gil J., Figueredo M. A., De la Concha E. G. Development of splenic natural suppressor (NS) cells in Ehrlich tumour-bearing mice. Int. J. Cancer 1989; 44: 307
  • Justo G. Z., Durán N., Queiroz M. L.S. Myelopoietic response in tumour-bearing mice by an aggregated polymer isolated from Aspergillus oryzae. Eur. J. Pharmacol. 2000; 388: 219
  • Valadares M. C., Klein S. I., Zyngier S., Queiroz M. L.S. Growth and differentiation of bone marrow hematopoietic cells in mice bearing Ehrlich ascite tumor and treated with dicyclopentadienildichlorotitanium (IV). Int. J. Immunopharmacol. 1998; 20: 573
  • Queiroz M. L.S., Justo G. Z., Valadares M. C., Pereira-da-Silva F. R.R., Müller A. Adjuvant effect of Pluchea quitoc extract on the resistance of tumor-bearing mice by modulation of the host hematopoietic response. Immunopharmacol. Immunotoxicol. 2001; 23: 215
  • Justo G. Z., Silva M. R., Queiroz M. L.S. Effects of Chlorella vulgaris on the response of the host hematopoietic system to intraperitoneal Ehrlich ascites tumor transplantation in mice. Immunopharmacol. Immunotoxicol. 2001; 23: 119
  • Keeb G., Lala P. K. Effect of Ehrlich ascites tumour transplantation in mice on the distribution of cells capable of forming hemopoietic colonies in vitro. Eur. J. Cancer 1978; 14: 331
  • Pessina A., Brambilla P., Villa S., Marocchi A., Mocarelli P. Factors produced by macrophages and tumour cells: Influence on the granulocytic precursor cells (CFU-C) in normal and tumour bearing mice. J. Cancer Res. Clin. Oncol. 1982; 102: 235
  • Pessina A., Brambilla P., Villa S., Mocarelli P. CFU-S and CFU-C proliferation after treatment of normal bone marrow cells with Ehrlich ascitic fluid. Oncology 1982; 39: 391
  • Spitalny G. L., North R. J. Subversion of host defense mechanisms by malignant tumours: an established tumour as a privileged site for bacterial growth. J. Exp. Med. 1977; 145: 1264
  • North R. J., Kirstein D. P., Tuttle R. L. Subversion of host defense mechanisms by murine tumours. I. A circulating factor that suppresses macrophage-mediated resistance to infection. J. Exp. Med. 1976; 143: 559
  • Mackaness G. B. Cellular resistance to infection. J. Exp. Med. 1962; 116: 381
  • 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
  • Wing E. J., Barczynski L. K., Waheed A., Shadduck R. K. Effect of Listeria monocytogenes 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
  • 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
  • Jones D. Foodborne listeriosis. Lancet 1990; 336: 1171
  • North R. J., Conlan J. W. Immunity to Listeria monocytogenes. Chem. Immunol. 1998; 70: 1
  • Chabner B. A., Myers C. E. Cancer, Principles and Practice of Oncology, V. T. DeVita, Jr., S. Hellman, S. A. Rosenberg. Lippincott, Philadelphia 1993; 374
  • Pizzo P. A. Granulocytopenia and cancer therapy. Past problems, current solutions, future challenges. Cancer 1984; 54: 2649
  • 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., Justo G. Z., Pereira-da-Silva F. R.R., Müller A. H., Guilhon G. M.S.P. Stimulatory action of Pluchea quitoc extract on the hematopoietic response during murine listeriosis. Immunopharmacol. Immunotoxicol., Immunopharmacol. Immunotoxicol. 2000; 22: 721
  • Melo A., Justo G. Z., Queiroz M. L.S. Stimulation of myelopoiesis in L. monocytogenes-infected mice by an aggregated polymer isolated from A. oryzae. Human Exp. Toxicol. 2001; 20: 38
  • Hamburger M., Hostettmann K. Bioactivity in plants: the link between phytochemistry and medicine. Phytochem. 1991; 30: 3864
  • Cruz G. L. Livro Verde das Plantas Medicinais e Industriais do Brasil. Belo Horizonte 1965; 1 e 2
  • Bacchi E. M., Sertié J. A.A., Villa N., Katz H. Antiulcer action and toxicity of Styrax camporum and Caesalpinia ferrea. Planta Med. 1995; 61: 204
  • Bacchi E. M., Sertié J. A.A. Antiulcer action and toxicity of Styrax camporum and Caesalpinia ferrea in rats. Planta Med. 1994; 60: 118
  • Carvalho J. C., Teixeira J. R., Souza P. J., Bastos J. K., dos Santos Filho D., Sarti S. J. Preliminary studies of analgesic and anti-inflammatory properties of Caesalpinia ferrea crude extract. J. Ethnopharmacol. 1996; 53: 175
  • Hikino H., Taguchi T., Fujimura H., Hiramatsu Y. Antiinflammatory principles of Caesalpinia sappan wood and of Haematoxylon campechianum wood. Planta Med. 1977; 31: 214
  • Montgomery R., Yamauchi F. Cesalin-an anti-neoplastic protein. Lloydia 1977; 40: 269
  • 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 Hemopoietic Colony Stimulating Factors. Elsevier, New York 1984
  • Kaufmann S. H.E. Immunity to intracellular microbial pathogens. Immunol. Today 1995; 16: 338
  • Milon G. Listeria monocytogenes in laboratory mice: a model of short-term infections and pathogenic process controllable by regulated protective immune responses. Immunol. Rev. 1997; 158: 37
  • North R. J., Dunn P. L., Conlan J. W. Murine listeriosis as a model of antimicrobial defense. Immunol. Rev. 1997; 158: 27
  • 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
  • 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
  • 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
  • Lepay D. A., Steinman R. M., Nathan C. F., Murray H. W., Cohn Z. A. Liver macrophages in murine listeriosis. Cell-mediated immunity is correlated with an influx of macrophages capable of generating reactive oxygen intermediates. J. Exp. Med. 1985; 161: 1503
  • 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
  • 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
  • Beller B. I., Ho K. Regulation of macrophage populations. V. Evaluation of the control of macrophage Ia expression in vitro. J. Immunol. 1982; 129: 971
  • Myata M., Mitsuyama M., Ogata N., Nomoto K., Takeya K. Two steps in the generation of acquired resistance against Listeria monocytogenes: accumulation and activation of macrophages. Immunology 1982; 47: 247
  • Czuprynski C. J., Henson P. M., Campbell P. A. Enhanced accumulation of inflammatory neutrophils and macrophage mediated by transfer of T cells from 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
  • 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
  • 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
  • Kumagai H., Masuda T., Sakashita M., Ishizuka M., Takeuchi T. Modulation of macrophage activity in tumour-bearing mice by cytogenin. J. Antibiot. 1995; 48: 321
  • Moore S. C., Theus S. A., Barnett J. B., Soderberg L. S. Bone marrow natural suppressor cells inhibit the growth of myeloid progenitor cells and synthesis of colony-stimulating factors. Exp. Hematol. 1992; 20: 1178
  • Parker A. N., Pragnell I. B. Inhibitors of haemopoiesis and their potential clinical relevance. Blood Rev. 1995; 9: 226

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.