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The use of SR - FTIR microspectroscopy for a preliminary biochemical study of the rat hippocampal formation tissue in case of pilocarpine induced epilepsy and neutroprotection with FK- 506

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Warianty tytułu
Konferencja
Proceedings of the International Conference on Development and Applications of Nuclear Technologies NUTECH-2011, 11-14 September 2011, Kraków, Poland
Języki publikacji
EN
Abstrakty
EN
The main aim of the work was the biochemical analysis of the hippocampal formation tissue in the case of epileptic rats treated with the neuroprotective agent FK-506. Three groups of animals were compared: rats with pilocarpine induced seizures treated and non-treated with tacrolimus as well as naive controls. Synchrotron radiation Fourier transform infrared (SR-FTIR) microspectroscopy was used for the biomolecular analysis of studied samples. The measurements were carried out at SISSI beamline of ELETTRA. A Bruker IFS 66v/S interferometer coupled to a Bruker Hyperion 2000 microscope was used. The tissue samples were analyzed in transmission mode with a beam defined by a small aperture and spatial resolution steps of 10 mi m which allowed us to probe the selected cross-line of the sample at cellular resolution. The obtained results enabled to compare the distributions of proteins and lipids in the three hippocampal cellular layers, i.e. in molecular, multiform and granular layers. For epileptic animals both treated and non-treated with FK-506, the tendency for increase of the ratio of the absorbance at around 1548 and 1658 cm-1 (amide II/amide I ratio) was observed, however only for the multiform layer these changes were statistically significant. Similar relation was noticed in case of the ratio of the absorbance at around 1631 and 1658 cm-1. The mentioned results may suggest conformational changes of proteins in the direction of beta-sheet secondary structure. Additionally, a statistically significant increase in the lipid massif and a decrease of the ratio of absorbance at around 2921 and 2958 cm-1 were observed for epileptic animals treated with tacrolimus comparing to the control group.
Czasopismo
Rocznik
Strony
615--619
Opis fizyczny
Bibliogr. 28 poz., rys.
Twórcy
autor
autor
autor
autor
autor
  • AGH University of Science and Technology, Faculty of Physics and Applied Computer Science, al. A. Mickiewicza 30, 30-059 Krakow, Poland, Tel.: +48 12 617 4424, Fax: +48 12 634 0010, dudala@novell.ftj.agh.edu.pl
Bibliografia
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  • 4. Chwiej J, Dulińska J, Janeczko K et al. (2010) Synchrotron FTIR microspectroscopy study of the rat hippocampal formation after pilocarpine-evoked seizures. J Chem Neuroanat 40:140–147
  • 5. Chwiej J, Janeczko K, Marciszko M, Czyzycki M, Rickers K, Setkowicz Z (2010) Neuroprotective action of FK-506 (tacrolimus) after seizures induced with pilocarpine: quantitative and topographic elemental analysis of brain tissue. Biol Inorg Chem 15:283–289
  • 6. Chwiej J, Winiarski W, Ciarach M et al. (2008) The role of trace elements in the pathogenesis and progress of pilocarpine-induced epileptic seizures. J Biol Inorg Chem 13:1267–1274
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  • 8. Dreissig I, Machill S, Salzer R, Krafft C (2009) Quantification of brain lipids by FTIR spectroscopy and partial least squares regression. Spectrochim Acta A 71:2069–2075
  • 9. Freitas RM (2009) Investigation of oxidative stress involvement in hippocampus in epilepsy model induced by pilocarpine. Neurosci Lett 462:225–229
  • 10. Freitas RM, Nascimento KG, Ferreira PMP, Jordan J (2009) Neurochemical changes on oxidative stress in rat hippocampus during acute phase of pilocarpine-induced seizures. Pharmacol Biochem Behav (doi:10.1016/j.pbb.2009.09.015)
  • 11. Freitas RM, Souza FCF, Vasconcelos SMM, Viana GSB, after status epilepticus in rats. FEBS J 272:1307–1312
  • 12. Furuichi Y, Maeda M, Moriguchi A et al. (2003) Tacrolimus, a potential neuroprotective agent, ameliorates ischemic brain damage and neurologic deficits after focal cerebral ischemia in nonhuman primates. J Cereb Blood Flow Metab 23:1183–1194
  • 13. Gallant M, Rak M, Szeghalmi A et al. (2006) Focally elevated creatine detected in amyloid precursor protein (APP) transgenic mice and Alzheimer disease brain tissue. J Biol Chem 281:5–8
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  • 15. Kneipp J, Miller L, Joncic M et al. (2003) In situ identification of protein structural changes in prion-infected tissue. Biochim Biophys Acta 1639:152–158
  • 16. Kretlow A (2007) Imaging molecular and trace element changes in scrapie-infected nervous tissue with a time course study. Dissertation zur Erlangung des Akademischen Grades des Doktors der Naturwissenschaften,Fachbereich Biologie, Chemie, Pharmazie der Freien Universitaet Berlin
  • 17. Kretlow A, Wang Qi, Kneipp J et al. (2006) FTIR-microspectroscopy of prion-infected nervous tissue. Biochim Biophys Acta 1758:948–959
  • 18. Miller LM, Dumas P (2010) From structure to cellular mechanism with infrared microspectroscopy. Curr Opin Struc Biol 20:649–656
  • 19. Peternel S, Pilipović K, Župan G (2009) Seizure susceptibility and the brain regional sensitivity to oxidative stress in male and female rats in the lithium-pilocarpine model of temporal lobe epilepsy. Prog Neuro-Psychopharmacol Biol Psychiatry 33:456–462
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  • 22. Setkowicz Z, Ciarach M, Guzik R, Janeczko K (2004) Different effects of neuroprotectants FK-506 and cyclosporin A on susceptibility to pilocarpine-induced seizures in rats with brain injured at different developmental stages. Epilepsy Res 61:63–72
  • 23. Skaper SD, Floreani M, Ceccon M, Facci L, Giusti P (1999) Excitotoxicity, oxidative stress, and neuroprotective potential of melatonin. Ann NY Acad Sci 890:107–118
  • 24. Tejada S, Roca C, Sureda A, Rial RV, Gamundí A, Esteban S (2006) Antioxidant response analysis in the brain after pilocarpine treatments. Brain Res Bull 69:587–592
  • 25. Tejada S, Sureda A, Roca C, Gamundi A, Esteban S (2007) Antioxidant response and oxidative damage in brain cortex after high dose of pilocarpine. Brain Res Bull 71:372–375
  • 26. Turski WA, Cavalheiro EA, Bortolotto ZA, Mello LM, Schwarz M, Turski L (1985) Seizures produced by pilocarpine in mice: a behavioral, electroencephalographic and morphological analysis. Brain Res 12:237–253
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Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ8-0023-0058
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