Bulletin of Experimental Biology and Medicine

, Volume 158, Issue 2, pp 278–283 | Cite as

Structural Changes in the Thymus in Allogenic Pregnancy in Mice with High Incidence of Spontaneous and Muramylpeptide-Induced Abortions

  • K. A. Artem’eva
  • M. N. Boltovskaya
  • O. V. Kalyuzhin
Article

Structural changes in the thymus over the course of allogenic pregnancy were studied in mice from highly fertile couples (CBA females and BALB/c males), animals with high spontaneous abortions (CBA females and DBA/2 males), and in experimental immunity-dependent pregnancy loss induced by muramyldipeptide β-heptylglycoside. Accidental involution of the thymus on days 8 and 14 of pregnancy was more pronounced in mice with high level of spontaneous embryo resorption than in females from highly fertile couples. Muramyldipeptide glycoside stimulated manifestations of thymus involution in fertile and “abortogenic” cross-breeding.

Key Words

mouse abortion models accidental involution of thymus muramyldipeptide β-heptylglycoside 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    K. A. Artem’eva, M. N. Boltovskaya, and O. V. Kalyuzhin, Kursk. Nauch.-Pract. Vestn. “Chelovek Ego Zdorov’e”, No. 2, 34–40 (2012).Google Scholar
  2. 2.
    A. E. Zemlyakov, V. V. Tsikalov, O. V. Kalyuzhin, et al., Bioorgan. Khim., 29, No. 3, 316–322 (2003).Google Scholar
  3. 3.
    A. E. Zemlyakov and V. Ya. Chirva, Khim. Prirod. Soed., No. 5, 714–718 (1987).Google Scholar
  4. 4.
    O. V. Kalyuzhin, A. E. Zemlyakov, E. V. Kalyuzhina, et al., Bull. Exp. Biol. Med., 134, No. 2, 161–164 (2002).PubMedCrossRefGoogle Scholar
  5. 5.
    O. V. Kalyuzhin, N. G. Kalina, A. F. Bashtanenko, et al., Bull. Exp. Biol. Med., 135, No. 5, 452–455 (2003).PubMedCrossRefGoogle Scholar
  6. 6.
    O. V. Kalyuzhin, M. V. Nelyubov, E. V. Kalyuzhina, et al., Bull. Exp. Biol. Med., 134, No. 3, 281-283(2002).PubMedCrossRefGoogle Scholar
  7. 7.
    A. V. Karaulov, O. V. Kalyuzhin, and A. E. Zemlyakov, Ross. Bioterapevtich. Zh., 1, No. 1, 14–24 (2002).Google Scholar
  8. 8.
    L. P. Mikhailova, O. V. Makarova, O. V. Kalyuzhin, et al., Immunologiya, 25, No. 3, 152–154 (2004).Google Scholar
  9. 9.
    A. N. Russkova, E. A. Lebedinskaya, and O. V. Lebedinskaya, Uspekhi Sovrem. Estestvoznan., No. 7, 52–53 (2010).Google Scholar
  10. 10.
    D. A. Clark and G. Chaouat, J. Reprod. Immunol., 96, Nos. 1–2, 1–7 (2012).PubMedCrossRefGoogle Scholar
  11. 11.
    M. E. Cortina, S. Litwin, M. E. Roux, and S. Miranda, Reprod. Fertil. Dev., 24, No. 8, 1123–1133 (2013).CrossRefGoogle Scholar
  12. 12.
    J. Kwak-Kim, J. C. Park, H. K. Ahn, et al., Am. J. Reprod. Immunol., 63, No. 6, 611–623 (2010).PubMedCrossRefGoogle Scholar
  13. 13.
    N. Watanabe, Y. H. Wang, H. K. Lee, et al., Nature, 436, 1181–1185 (2005).PubMedCrossRefGoogle Scholar
  14. 14.
    A. L. Zoller, F. J. Schnell, and G. J. Kersh, Immunology, 121, No. 2, 207–215 (2007).PubMedCentralPubMedCrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media New York 2014

Authors and Affiliations

  • K. A. Artem’eva
    • 1
  • M. N. Boltovskaya
    • 1
  • O. V. Kalyuzhin
    • 1
  1. 1.Laboratory of Cellular Immunopathology and BiotechnologyResearch Institute of Human Morphology, the Russian Academy of Medical SciencesMoscowRussia

Personalised recommendations