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Journal of Biomedicine and Biotechnology
Volume 2011 (2011), Article ID 625380, 10 pages
http://dx.doi.org/10.1155/2011/625380
Research Article

Sex Steroids Effects on the Molting Process of the Helminth Human Parasite Trichinella spiralis

1Departamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, 04510 México, DF, Mexico
2Subdirección de Investigación Básica, Instituto Nacional de Cancerología, Secretaría de Salud, 14080 México, DF, Mexico
3Departamento de Inmunología e Infectología Pediátrica, Instituto Nacional de Pediatría, Secretaría de Salud, 11000 México, DF, Mexico
4Departamento de Biología, Facultad de Química, Universidad Nacional Autónoma de México, 04510, Mexico
5Departamento de Psicoinmunología, Instituto Nacional de Psiquiatría “Ramón de la Fuente”, 14370 México, DF, Mexico

Received 28 March 2011; Revised 18 August 2011; Accepted 23 August 2011

Academic Editor: Luis I. Terrazas

Copyright © 2011 Romel Hernández-Bello et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. D. H. Olster and J. D. Blaustein, “Development of steroid-induced lordosis in female guinea pigs: effects of different estradiol and progesterone treatments, clonidine, and early weaning,” Hormones and Behavior, vol. 23, no. 1, pp. 118–129, 1989. View at Scopus
  2. D. W. Pfaff, M. M. Freidin, X. S. Wu-Peng, J. Yin, and Y. S. Zhu, “Competition for DNA steroid response elements as a possible mechanism for neuroendocrine integration,” Journal of Steroid Biochemistry and Molecular Biology, vol. 49, no. 4–6, pp. 373–379, 1994. View at Publisher · View at Google Scholar · View at Scopus
  3. E. Cabrera-Muñoz, A. González-Arenas, M. Saqui-Salces et al., “Regulation of progesterone receptor isoforms content in human astrocytoma cell lines,” Journal of Steroid Biochemistry and Molecular Biology, vol. 113, no. 1-2, pp. 80–84, 2009. View at Publisher · View at Google Scholar · View at Scopus
  4. G. Escobedo, C. W. Roberts, J. C. Carrero, and J. Morales-Montor, “Parasite regulation by host hormones: an old mechanism of host exploitation?” Trends in Parasitology, vol. 21, no. 12, pp. 588–593, 2005. View at Publisher · View at Google Scholar · View at Scopus
  5. C. Guerra-Araiza, A. Coyoy-Salgado, and I. Camacho-Arroyo, “Sex differences in the regulation of progesterone receptor isoforms expression in the rat brain,” Brain Research Bulletin, vol. 59, no. 2, pp. 105–109, 2002. View at Publisher · View at Google Scholar · View at Scopus
  6. P. Ascenzi, A. Bocedi, and M. Marino, “Structure-function relationship of estrogen receptor α and β: impact on human health,” Molecular Aspects of Medicine, vol. 27, no. 4, pp. 299–402, 2006. View at Publisher · View at Google Scholar · View at Scopus
  7. L. I. Terrazas, R. Bojalil, T. Govezensky, and C. Larraide, “A role for 17-β-estradiol in immunoendocrine regulation of murine cysticercosis (Taenia crassiceps),” Journal of Parasitology, vol. 80, no. 4, pp. 563–568, 1994. View at Scopus
  8. G. Escobedo, L. López-Griego, and J. Morales-Montor, “Neuroimmunoendocrine modulation in the host by helminth parasites: a novel form of host-parasite coevolution?” NeuroImmunoModulation, vol. 16, no. 2, pp. 78–87, 2009. View at Publisher · View at Google Scholar · View at Scopus
  9. O. Bottasso and J. Morales-Montor, “Neuroimmunomodulation during infectious diseases: mechanisms, causes and consequences for the host,” NeuroImmunoModulation, vol. 16, no. 2, pp. 65–67, 2009. View at Publisher · View at Google Scholar · View at Scopus
  10. H. S. Thabet, S. S. Thabet, N. M. Ali, and N. S. Ahmed, “Effects of ovariectomy and thyroidectomy on course and outcome of Trichinella spiralis infection in rat,” Journal of the Egyptian Society of Parasitology, vol. 38, no. 1, pp. 29–46, 2008. View at Scopus
  11. Y. Osorio, D. L. Bonilla, A. G. Peniche, P. C. Melby, and B. L. Travi, “Pregnancy enhances the innate immune response in experimental cutaneous leishmaniasis through hormone-modulated nitric oxide production,” Journal of Leukocyte Biology, vol. 83, no. 6, pp. 1413–1422, 2008. View at Publisher · View at Google Scholar · View at Scopus
  12. C. D. Santos, M. P. A. Toldo, F. H. Santello, M. D. V. Filipin, V. Brazão, and J. C. do Prado Júnior, “Dehydroepiandrosterone increases resistance to experimental infection by Trypanosoma cruzi,” Veterinary Parasitology, vol. 153, no. 3-4, pp. 238–243, 2008. View at Publisher · View at Google Scholar · View at Scopus
  13. J. Morales, T. Velasco, V. Tovar et al., “Castration and pregnancy of rural pigs significantly increase the prevalence of naturally acquired Taenia solium cysticercosis,” Veterinary Parasitology, vol. 108, no. 1, pp. 41–48, 2002. View at Publisher · View at Google Scholar · View at Scopus
  14. J. Morales-Montor, G. Escobedo, J. A. Vargas-Villavicencio, and C. Larralde, “The neuroimmunoendocrine network in the complex host-parasite relationship during murine cysticercosis,” Current Topics in Medicinal Chemistry, vol. 8, no. 5, pp. 400–407, 2008. View at Publisher · View at Google Scholar · View at Scopus
  15. N. Peña, J. Morales, J. Morales-Montor et al., “Impact of naturally acquired Taenia solium cysticercosis on the hormonal levels of free ranging boars,” Veterinary Parasitology, vol. 149, no. 1-2, pp. 134–137, 2007. View at Publisher · View at Google Scholar · View at Scopus
  16. F. W. Bazer, R. C. Burghardt, G. A. Johnson, T. E. Spencer, and G. Wu, “Interferons and progesterone for establishment and maintenance of pregnancy: interactions among novel cell signaling pathways,” Reproductive Biology, vol. 8, no. 3, pp. 179–211, 2008. View at Scopus
  17. G. Escobedo, C. Larralde, A. Chavarria, M. A. Cerbón, and J. Morales-Montor, “Molecular mechanisms involved in the differential effects of sex steroids on the reproduction and infectivity of Taenia crassiceps,” Journal of Parasitology, vol. 90, no. 6, pp. 1235–1244, 2004. View at Publisher · View at Google Scholar · View at Scopus
  18. J. Morales-Montor, S. Baig, C. Hallal-Calleros, and R. T. Damian, “Taenia crassiceps: androgen reconstitution of the host leads to protection during cysticercosis,” Experimental Parasitology, vol. 100, no. 4, pp. 209–216, 2002. View at Publisher · View at Google Scholar · View at Scopus
  19. J. A. Vargas-Villavicencio, C. Larralde, and J. Morales-Montor, “Gonadectomy and progesterone treatment induce protection in murine cysticercosis,” Parasite Immunology, vol. 28, no. 12, pp. 667–674, 2006. View at Publisher · View at Google Scholar · View at Scopus
  20. I. Bhai and A. K. Pandey, “Gonadal hormones in experimental Ancylostoma caninum infections in male Swiss albino mice,” International Journal for Parasitology, vol. 12, no. 6, pp. 589–591, 1982. View at Publisher · View at Google Scholar · View at Scopus
  21. L. Charniga, G. L. Stewart, G. W. Kramar, and J. A. Stanfield, “The effects of host sex on enteric response to infection with Trichinella spiralis,” Journal of Parasitology, vol. 67, no. 6, pp. 917–922, 1981. View at Scopus
  22. J. J. Reddington, G. L. Stewart, G. W. Kramar, and M. A. Kramar, “The effects of host sex and hormones on Trichinella spiralis in the mouse,” Journal of Parasitology, vol. 67, no. 4, pp. 548–555, 1981. View at Scopus
  23. V. Figallová and J. Prokopic, “The effects of host sex and sex hormones on Trichinella spiralis Owen, 1835 and T. pseudospiralis Garkavi, 1972 in the mouse,” Folia Parasitologica, vol. 35, no. 1, pp. 59–66, 1988.
  24. D. T. Dennis, D. D. Despommier, and N. Davis, “Infectivity of the newborn larva of Trichinella spiralis in the rat,” Journal of Parasitology, vol. 56, no. 5, pp. 974–977, 1970. View at Scopus
  25. R. Hernández-Bello, R. M. Bermúdez-Cruz, R. Fonseca-Liñán et al., “Identification, molecular characterisation and differential expression of caveolin-1 in Trichinella spiralis maturing oocytes and embryos,” International Journal for Parasitology, vol. 38, no. 2, pp. 191–202, 2008. View at Publisher · View at Google Scholar · View at Scopus
  26. M. K. Angele, M. G. Schwacha, A. Ayala, and I. H. Chaudry, “Effect of gender and sex hormones on immune responses following shock,” Shock, vol. 14, no. 2, pp. 81–90, 2000. View at Scopus
  27. C. W. Roberts, W. Walker, and J. Alexander, “Sex-associated hormones and immunity to protozoan parasites,” Clinical Microbiology Reviews, vol. 14, no. 3, pp. 476–488, 2001. View at Publisher · View at Google Scholar · View at Scopus
  28. S. L. Klein, “The effects of hormones on sex differences in infection: from genes to behavior,” Neuroscience and Biobehavioral Reviews, vol. 24, no. 6, pp. 627–638, 2000. View at Publisher · View at Google Scholar · View at Scopus
  29. M. Zuk and K. A. McKean, “Sex differences in parasite infections: patterns and processes,” International Journal for Parasitology, vol. 26, no. 10, pp. 1009–1024, 1996. View at Publisher · View at Google Scholar · View at Scopus
  30. A. B. Kamis and J. B. Ibrahim, “Effects of testosterone on blood leukocytes in Plasmodium berghei-infected mice,” Parasitology Research, vol. 75, no. 8, pp. 611–613, 1989. View at Scopus
  31. E. M. de Souza, M. Rivera, T. C. Araújo-Jorge, and S. L. de Castro, “Modulation induced by estradiol in the acute phase of Trypanosoma cruzi infection in mice,” Parasitology Research, vol. 87, no. 7, pp. 513–520, 2001. View at Publisher · View at Google Scholar · View at Scopus
  32. J. C. Rivero, Y. Inoue, N. Murakami, and Y. Horii, “Androgen-and estrogen-dependent sex differences in host resistance to Strongyloides venezuelensis infection in Wistar rats,” Journal of Veterinary Medical Science, vol. 64, no. 6, pp. 457–461, 2002. View at Publisher · View at Google Scholar · View at Scopus
  33. R. M. F. Libonati, M. G. Cunha, J. M. Souza et al., “Estradiol, but not dehydroepiandrosterone, decreases parasitemia and increases the incidence of cerebral malaria and the mortality in Plasmodium berghei ANKA-infected CBA mice,” NeuroImmunoModulation, vol. 13, no. 1, pp. 28–35, 2006. View at Publisher · View at Google Scholar · View at Scopus
  34. G. Nuñez, T. Gentile, M. Calcagno, and S. Venturiello, “Increased parasiticide activity against Trichinella spiralis newborn larvae during pregnancy,” Parasitology Research, vol. 88, no. 7, pp. 661–667, 2002. View at Publisher · View at Google Scholar · View at Scopus
  35. G. G. Nuñez, T. Gentile, S. N. Costantino, M. I. Sarchi, and S. M. Venturiello, “In vitro and in vivo effects of progesterone on Trichinella spiralis newborn larvae,” Parasitology, vol. 131, no. 2, pp. 255–259, 2005. View at Publisher · View at Google Scholar · View at Scopus
  36. A. Barrabes, J. Goma-Mouanda, F. Reynouard, and C. Combescot, “17 beta-estradiol receptors in Schistosoma mansoni. Contribution to the explanation of the protective power of this hormone in Schistosoma mansoni bilharziasis in the mouse. Preliminary study,” Annales de Parasitologie Humaine et Comparee, vol. 61, no. 6, pp. 637–641, 1986. View at Scopus
  37. T. E. Hood, E. J. Calabrese, and B. M. Zuckerman, “Detection of an estrogen receptor in two nematode species and inhibition of binding and development by environmental chemicals,” Ecotoxicology and Environmental Safety, vol. 47, no. 1, pp. 74–81, 2000. View at Publisher · View at Google Scholar · View at Scopus
  38. R. T. Damian, “Parasite immune evasion and exploitation: reflections and projections,” Parasitology, vol. 115, pp. S169–S175, 1997.
  39. M. Shibayama, J. D. J. Serrano-Luna, S. Rojas-Hernández, R. Campos-Rodríguez, and V. Tsutsumi, “Interaction of secretory immunoglobulin A antibodies with Naegleria fowleri trophozoites and collagen type I,” Canadian Journal of Microbiology, vol. 49, no. 3, pp. 164–170, 2003. View at Publisher · View at Google Scholar · View at Scopus
  40. F. Remoué, J. C. Mani, M. Pugnière, A. M. Schacht, A. Capron, and G. Riveau, “Functional specific binding of testosterone to Schistosoma haematobium 28-kilodalton glutathione S-transferase,” Infection and Immunity, vol. 70, no. 2, pp. 601–605, 2002. View at Publisher · View at Google Scholar · View at Scopus
  41. C. Konrad, A. Kroner, M. Spiliotis, R. Zavala-Góngora, and K. Brehm, “Identification and molecular characterisation of a gene encoding a member of the insulin receptor family in Echinococcus multilocularis,” International Journal for Parasitology, vol. 33, no. 3, pp. 301–312, 2003. View at Publisher · View at Google Scholar · View at Scopus
  42. M. Spiliotis, C. Konrad, V. Gelmedin et al., “Characterisation of EmMPK1, an ERK-like MAP kinase from Echinococcus multilocularis which is activated in response to human epidermal growth factor,” International Journal for Parasitology, vol. 36, no. 10-11, pp. 1097–1112, 2006. View at Publisher · View at Google Scholar · View at Scopus
  43. K. Brehm and M. Spiliotis, “The influence of host hormones and cytokines on echinococcus multilocuiaris signalling and development,” Parasite, vol. 15, no. 3, pp. 286–290, 2008. View at Scopus