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Effects of Ionizing Radiation and Aluminum Chloride on Protein of Glial Intermediate Filaments in the Rat Brain

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Abstract

We studied the effects of irradiation with X-rays (the total dose of 0.0129 C/kg was attained over 7, 14, or 21 days), increased entry of Al3+ into the organism (0.2% AlCl3 in drinking water), and the combined influence of these factors for 21 days on the contents of the soluble and filamentous forms of glial fibrillary acidic protein (GFAP) in the tissues of the hippocampus, cerebellum, and neocortex of albino rats. After irradiation for 7 days, a clear trend toward drops in the GFAP contents in the structures under study was observed, while irradiation in the same dose, but for 14 or 21 days, resulted in increases in the contents of both GFAP forms (within a range of 13-29%, as compared with the control). Entry of aluminum chloride with water also resulted in an increase in the GFAP contents in all studied structures; changes in the filamentous form were more intensive. The combined influence of irradiation and Al3+ resulted in more intensive shifts in the GFAP levels; the content of its filamentous form increased in all structures by about 50%, while shifts of the soluble form were somewhat smaller.

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REFERENCES

  1. B. A. Berezin, G. M. Shevchenko, G.G. Bunyatyan, et al., “Spe-cific proteins of intermediate filaments in normal nerve tissue and in brain tumors,” Neirokhimiya, 6, No. 2, 77-82 (1987).

    Google Scholar 

  2. B. Holmberg, L. Rosengren, J. E. Karlsson, and B. Johnels, “ln-creased cerebrospinal fluid levels of neurofilament protein in pro-gressive supranuclear palsy and multiple-system atrophy compared with Parkinson's disease,” Movement Disorders, 13, No. 1, 70-77 (1996).

    Google Scholar 

  3. B. Inoue, S. Yagishi, Y. Hoh, et al., “Coexistence of paired helical filaments and polyglucosan bodies in the same neuron in an autopsy case of Alzheimer's disease,” Acta Neuropathol., 90, No. 5, 511-514 (1996).

    Google Scholar 

  4. M. Yamszaki, I. Nakano, O. Imazu, and A. Terashi, “Paired helical filaments and straight tubules in astrocytes: an electron microscopic study in dementia of the Alzheimer type,” Acta Neuropathol., 90, No. 1, 31-36 (1995).

    Google Scholar 

  5. V. S. Nedzvetskii, S. G. Busygina, V. A. Berezin, and A. I. Dvoretskii, “CNS syndrome. Characterization of the intermediate filaments in the rat brain,” Radiobiologiya, 30, Issue 2, 243-246 (1990).

    Google Scholar 

  6. V. S. Nedzvetskii, G. A. Ushakova, S. G. Busygina, et al., “Effect of small doses of ionizing radiation on the intermediate filaments and Ca 2+-activated system of proteolysis in the rat brain,” Radio-biologiya, 31, Issue 3, 333-339 (1991).

    Google Scholar 

  7. J. F. Leterier, D. Langui, A. Probst, and I. Ulrich, “A molecular mechanism for the induction of neurofilament bundling by aluminium ions,” J. Neurochem., 58, 755-760 (1992).

    Google Scholar 

  8. V. S. Nedzvetskii, V. A. Berezin, T. I. Obernyak, and E. N. Zhmareva, “Characterization of specific proteins of the intermediate filaments in brain tumors of humans,” Biokhimiya, 51, No. 11, 1843-1850 (1986).

    Google Scholar 

  9. G. L. Miller, “Protein determination for large numbers of samples,” Anal. Chem., 31, No. 5, 964-966 (1959).

    Google Scholar 

  10. V. S. Nedzvetskii and P. A. Nerush, “Protein of the glial intermediate filaments in different regions of the rat brain in experimental neurosis,” Neirofiziologiya/Neurophysiology, 31, No. 2, 115-119 (1999).

    Google Scholar 

  11. Z. Somosy, M. Sass, G. Bognar, et al., “X-irradiation-induced disorganization of cytoskeletal filaments and cell contacts in HT29 cells,” Scanning Microscopy, 9, No. 3, 763-772 (1995).

    Google Scholar 

  12. T. B. Shea, M. L. Beermann, and R. A. Nixon, “Aluminium treatment of intact neuroblastoma cells alters neurofilament subunit phosphorylation, solubility, and proteolysis,” Mol. Clin. Neuropathol., 26, No. 1, 1-14 (1995).

    Google Scholar 

  13. E. Petersen, H. V. Nielsen, L. Christiansen, and J. Spenter, “Immunization with E. coli produced recombinant T. gondii SHG1 with alum as adjuvant to protect mice against lethal infection with Toxoplasma gondii,” Vaccine, 16, No. 13, 1283-1289 (1998).

    Google Scholar 

  14. M. G. Tari, M. Mancino, E. Ghezi, et al., “Immunotherapy with an alum adsorbed parietoria-pollen allergoid: a 2-year, double-blind, placebo-controlled study,” Eur. J. Allergy Clin. Immunol., 52, No. 1, 65-74 (1997).

    Google Scholar 

  15. W. F. Huff, P. A. Moore, J. M. Balog, et al., “Evaluation of the toxicity of alum (alum sulfate) in young broiler chickens,” Poultry Sci., 75, No. 11, 1359-1365 (1996).

    Google Scholar 

  16. G. Pagano, E. His, R. Beiras, et al., “Cytogenetic, developmental, and biochemical effects of aluminium, iron, and their mixture in sea urchins and mussels,” Arch. Environment. Contaminat. Toxicol., 31, No. 4, 466-474 (1996).

    Google Scholar 

  17. T. Shea, J. Clarke, T. Whelock, et al., “Aluminium salts induce the accumulation of neurofilaments in perykaryal of NB 2a/dl neuro-blastoma,” Brain Res., 14, No. 5, 53-64 (1998).

    Google Scholar 

  18. W. Jeglinski, D. Koczuk, M. Zaremba, et al., “Bilateral gliosis in unilaterally lesioned septohippocampal system: changes in GFAP immunoreactivity and content,” J. Neurosci. Res., 41, No. 3, 394-402 (1995).

    Google Scholar 

  19. R. A. Yokel and J. P. O'Calladhan, “An aluminium-induced in-crease in GFAP is attenuated by some chelators,” Neurotoxicol. Teratol., 20, No. 1, 55-60 (1998).

    Google Scholar 

  20. Z. Gong, A. R. Little, H. el-Fawal, and H. L. Evans, “Trimethyl lead neurotoxicity in the rat: changes in glial fibrillary acidic protein,” Arh. Aigijenu Rada Toksikol., 46, No. 4, 381-390 (1995).

    Google Scholar 

  21. C. W. MacDiarmid and R. C. Gardner, “Al3+ toxicity in yeast. A role for Mg2+?” Plant Physiol., 112, No. 3, 1101-1109 (1996).

    Google Scholar 

  22. B. P. He and M. J. Strong, “A morphological analysis of motor neuron degeneration and microglial reaction in acute and chronic in vivo aluminium chloride neurotoxicity,” J. Chem. Neuroanat., 17, No. 4, 207-215 (2000).

    Google Scholar 

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Nedzvetskii, V.S., Nerush, P.A., Tikhomirov, A.A. et al. Effects of Ionizing Radiation and Aluminum Chloride on Protein of Glial Intermediate Filaments in the Rat Brain. Neurophysiology 33, 28–33 (2001). https://doi.org/10.1023/A:1010460130068

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