Skip to main content
Log in

Thioredoxin-1 expression levels in rat hippocampal neurons in moderate hypobaric hypoxia

  • Published:
Neuroscience and Behavioral Physiology Aims and scope Submit manuscript

Previous studies have demonstrated that preconditioning (PC) with three sessions of moderate hypoxia significantly increases the expression of the antioxidant protein thioredoxin-1 (Trx-1) in the rat hippocampus by 3 h after subsequent acute severe hypoxia as compared with non-preconditioned animals. However, it remained unclear whether this increase in Trx-1 accumulation during PC is induced before severe hypoxia or is a modification of the response to severe hypoxia. This question was addressed in the present investigation using experiments on 12 adult male Wistar rats with studies of Trx-1 expression after PC without subsequent severe hypoxia. Immunocytochemical studies were performed 3 and 24 h after three episodes of moderate hypobaric hypoxia (three sessions of 2 h at 360 mmHg with 24-h intervals). Immunoreactivity to Trx-1 24 h after the last session was significantly decreased in neurons in all the areas of the hippocampus studied (CA1, CA2, CA3, and the dentate gyrus). Immunoreactivity in CA3 was also decreased 3 h after hypoxia. These results provide evidence that moderate preconditioning hypoxia itself not only does not increase, but even significantly decreases Trx-1 expression. Thus, increases in Trx-1 contents in the hippocampus of preconditioned animals after severe hypoxia are not associated with the accumulation of this protein during PC, but with a PC-induced modification of the reaction to severe hypoxia.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. L. A. Vataeva, E. A. Tyul'kova, and M. O. Samoilov, “Effects of prior exposure to moderate hypoxia on impairments to the acquisition and reproduction of a conditioned passive avoidance reaction induced by severe hypobaric hypoxia in rats,” Zh. Vyssh. Nerv. Deyat., 54, No. 6, 795–801 (2004).

    Google Scholar 

  2. M. O. Samoilov, E. V. Lazarevich, D. G. Semenov, et al., “Adaptive effects of hypoxic preconditioning of brain neurons,” Ros. Fiziol. Zh., 87, No. 6, 714–729 (2001).

    CAS  Google Scholar 

  3. M. O. Samoilov, E. A. Rybnikova, E. I. Tyul'kova, et al., “Mitochondrial antioxidants thioredoxin-2 and Mn superoxide dismutase are involved in the mechanisms of hypoxic tolerance of the brain,” Dokl. Ros. Akad. Nauk., 387, No. 3, 1–4 (2002).

    Google Scholar 

  4. T. Andoh, P. B. Chock, and C. C. Chiueh, “The roles of thioredoxin in protection against oxidative stress-induced apoptosis in SH-SY5Y cells,” Biol. Chem., 277, 9655–9660 (2002).

    Article  CAS  Google Scholar 

  5. D. K. Das, N. Maulik, M. Sato, and P. S. Ray, “Reactive oxygen species function as second messenger during ischemic preconditioning of heart,” Mol. Cell. Biochem., 196, 59–67 (1999).

    Article  PubMed  CAS  Google Scholar 

  6. K. C. Das, Y. Lewis-Molock, and C. W. White, “Elevation of manganese superoxide dismutase gene expression by thioredoxin,” Amer. J. Respir. Cell. Mol. Biol., 17, 713–726 (1997).

    CAS  Google Scholar 

  7. I. Hattori, Y. Takagi, K. Nozaki, et al., “Hypoxia-ischemia induces thioredoxin expression and nitrotyrosine formation in new-born rat brain,” Redox. Rep., 7, 256–259 (2002).

    Article  PubMed  CAS  Google Scholar 

  8. K. Kitagawa, M. Matsumoto, M. Tagaya, et al., “'Ischemic tolerance’ phenomenon found in the brain,” Brain Res., 528, 21–24 (1990).

    Article  PubMed  CAS  Google Scholar 

  9. A. Patenaude, M. R. Murthy, and M. E. Mirault, “Emerging roles of thioredoxin cycle enzymes in the central nervous system,” Cell. Mol. Life Sci., 62, 1063–1080 (2005).

    Article  PubMed  CAS  Google Scholar 

  10. C. Rauca, R. Zerbe, H. Jantze, and M. Krug, “The importance of free hydroxyl radicals to hypoxia preconditioning,” Brain Res., 868, 147–149 (2000).

    Article  PubMed  CAS  Google Scholar 

  11. A. Ravati, B. Ahlemeyer, A. Becker, et al., “Preconditioning-induced neuroprotection is mediated by reactive oxygen species and activation of the transcription factor-κB,” J. Neurochem., 78, 909–919 (2001).

    Article  PubMed  CAS  Google Scholar 

  12. E. Rybnikova, N. Sitnik, T. Gluschenko, et al., “The preconditioning modified neuronal expression of apoptosis-related proteins of Bcl-2 superfamily following severe hypobaric hypoxia in rats,” Brain Res., 1089, 195–202 (2006).

    Article  PubMed  CAS  Google Scholar 

  13. E. Rybnikova, L. Vataeva, E. Tyulkova, et al., “Mild hypoxia preconditioning prevents impairment of passive avoidance learning and suppression of brain NGFI-A expression induced by severe hypoxia,” Behav. Brain Res., 160, 107–114 (2005).

    Article  PubMed  CAS  Google Scholar 

  14. S. A. Stroev, T. S. Gluschenko, E. I. Tyulkova, et al., “Preconditioning enhances the expression of mitochondrial antioxidant thioredoxin-2 in the forebrain of rats exposed to severe hypobaric hypoxia,” Neurosci. Res., 78, 563–569 (2004).

    Article  CAS  Google Scholar 

  15. S. A. Stroev, T. S. Gluschenko, E. I. Tyulkova, et al., “The effect of preconditioning on the Cu,Zn superoxide dismutase expression and enzyme activity in rat brain at the early period after severe hypobaric hypoxia,” Neurosci. Res., 53, 39–47 (2005).

    Article  PubMed  CAS  Google Scholar 

  16. S. A. Stroev, E. U. Tjulkova, T. S. Gluschenko, et al., “The augmentation of brain thioredoxin-1 expression after severe hypobaric hypoxia by the preconditioning in rats,” Neurosci. Lett., 370, 224–229 (2004).

    Article  PubMed  CAS  Google Scholar 

  17. Y. Takagi, E. Horikawa, K. Nozaki, et al., “Expression and distribution of redox regulatory protein, thioredoxin during transient focal brain ischemia in the rat,” Neurosci. Lett., 251, 25–28 (1998).

    Article  PubMed  CAS  Google Scholar 

  18. Y. Takagi, A. Matsui, A. Nishiyama, et al., “Overexpression of thioredoxin in transgenic mice attenuates focal ischemic brain damage,” Proc. Natl. Acad. Sci. USA, 96, 4131–4136 (1999).

    Article  PubMed  CAS  Google Scholar 

  19. S. Udea, H. Masutani, J. Nakamura, et al., “Redox control of cell death,” Antioxid. Redox. Signal., 4, 405–414 (2002).

    Article  Google Scholar 

  20. R. Yang, D. J. Weber, and F. Carrier, “Post-transcriptional regulation of thioredoxin by the stress inducible heterogeneous ribonucleoprotein A18,” Nucl. Acids Res., 34, 1224–1236 (2006).

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Morfologiya, Vol. 133, No. 1, pp. 20–24, January–February, 2008.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Stroev, S.A., Tyul’kova, E.I., Glushchenko, T.S. et al. Thioredoxin-1 expression levels in rat hippocampal neurons in moderate hypobaric hypoxia. Neurosci Behav Physi 39, 1–5 (2009). https://doi.org/10.1007/s11055-008-9091-5

Download citation

  • Received:

  • Revised:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11055-008-9091-5

Key Words

Navigation