Field potential recording from rat hippocampus provides a functional evaluation method for assessing demyelination and myelin repair

References

• Houtchens MK, Lublin FD, Miller AE, Khoury SJ. Multiple sclerosis and other inflammatory demyelinating diseases of the central nervous system. In: , Daroff R, Mazziotta G, Fenichel G, Jankovic J eds. Bradley's Neurology in Clinical Practice, 6th Edition online version, Elsevier Health Care, 2012, pp. 1284–1302.
   Google Scholar
• Papadopoulos D, Dukes S, Patel R, Nicholas R, Vora A, Reynolds R. Substantial archaeocortical atrophy and neuronal loss in multiple sclerosis. Brain Pathol. 2009;19(2):238–53.
   PubMed Web of Science ®Google Scholar
• Woodruff RH, Franklin RJ. Demyelination and remyelination of the caudal cerebellar peduncle of adult rats following stereotaxic injections of lysolecithin, ethidium bromide, and complement/anti-galactocerebroside: a comparative study. Glia. 1999;25(3):216–28.
   PubMed Web of Science ®Google Scholar
• Stangel M, Hartung HP. Remyelinating strategies for the treatment of multiple sclerosis. Prog Neurobiol. 2002;68(5):361–76.
   PubMed Web of Science ®Google Scholar
• Franklin RJ. Why does remyelination fail in multiple sclerosis? Nat Rev Neurosci. 2002;3(9):705–14.
   PubMed Web of Science ®Google Scholar
• Pluchino S, Muzio L, Imitola J, Deleidi M, Alfaro-Cervello C, Salani G, et al.. Persistent inflammation alters the function of the endogenous brain stem cell compartment. Brain. 2008;131(Pt.10):2564–78.
   PubMed Web of Science ®Google Scholar
• Ernst C, Christie BR. Nestin-expressing cells and their relationship to mitotically active cells in the subventricular zones of the adult rat. Eur J Neurosci. 2005;22(12):3059–66.
   PubMed Web of Science ®Google Scholar
• Picard-Riera N, Nait-Oumesmar B, Baron-Van Evercooren A. Endogenous adult neural stem cells: limits and potential to repair the injured central nervous system. J Neurosci Res. 2004;76(2):223–31.
   PubMed Web of Science ®Google Scholar
• Mozafari S, Javan M, Sherafat MA, Mirnajafi-Zadeh J, Heibatollahi M, Pour-Beiranvand S, et al.. Analysis of structural and molecular events associated with adult rat optic chiasm and nerves demyelination and remyelination: possible role for 3rd ventricle proliferating cells. Neuromolecular Med. 2011;13(2):138–50.
   PubMed Web of Science ®Google Scholar
• Mozafari S, Sherafat MA, Javan M, Mirnajafi-Zadeh J, Tiraihi T. Visual evoked potentials and MBP gene expression imply endogenous myelin repair in adult rat optic nerve and chiasm following local lysolecithin induced demyelination. Brain Res. 2010;1351:50–6.
   PubMed Web of Science ®Google Scholar
• Palmer TD, Takahashi J, Gage FH. The adult rat hippocampus contains primordial neural stem cells. Mol Cell Neurosci. 1997;8(6):389–404.
   PubMed Web of Science ®Google Scholar
• Gensert JM, Goldman JE. Endogenous progenitors remyelinate demyelinated axons in the adult CNS. Neuron. 1997;19(1):197–203.
   PubMed Web of Science ®Google Scholar
• Doetsch F, Garcia-Verdugo JM, Alvarez-Buylla A. Cellular composition and three-dimensional organization of the subventricular germinal zone in the adult mammalian brain. J Neurosci. 1997;17(13):5046–61.
   PubMed Web of Science ®Google Scholar
• Chang A, Tourtellotte WW, Rudick R, Trapp BD. Premyelinating oligodendrocytes in chronic lesions of multiple sclerosis. N Engl J Med. 2002;346(3):165–73.
   PubMed Web of Science ®Google Scholar
• Soto A, Perez-Samartin AL, Etxebarria E, Matute C. Excitotoxic insults to the optic nerve alter visual evoked potentials. Neuroscience. 2004;123(2):441–9.
   PubMed Web of Science ®Google Scholar
• Kandel ER, Schwartz JH, Jessell TM. Principles of neural science. McGraw-Hill, Health Professions Division; 2000, 4th edition, New York, pages 1258–60.
   Google Scholar
• Nakatomi H, Kuriu T, Okabe S, Yamamoto S, Hatano O, Kawahara N, et al.. Regeneration of hippocampal pyramidal neurons after ischemic brain injury by recruitment of endogenous neural progenitors. Cell. 2002;110(4):429–41.
   PubMed Web of Science ®Google Scholar
• Koutsoudaki PN, Skripuletz T, Gudi V, Moharregh-Khiabani D, Hildebrandt H, Trebst C, et al.. Demyelination of the hippocampus is prominent in the cuprizone model. Neurosci Lett. 2009;451(1):83–8.
   PubMed Web of Science ®Google Scholar
• Jessberger S, Gage FH. Fate plasticity of adult hippocampal progenitors: biological relevance and therapeutic use. Trends Pharmacol Sci. 2009;30(2):61–5.
   PubMed Web of Science ®Google Scholar
• Paxinos G, Watson C. The rat brain in stereotaxic coordinates, 6th edn. Academic press, New York, 2006, F29.
   Google Scholar
• Pavelko KD, van Engelen BG, Rodriguez M. Acceleration in the rate of CNS remyelination in lysolecithin-induced demyelination. J Neurosci. 1998;18(7):2498–505.
   PubMed Web of Science ®Google Scholar
• Atkins CM, Yon M, Groome NP, Sweatt JD. Regulation of myelin basic protein phosphorylation by mitogen-activated protein kinase during increased action potential firing in the hippocampus. J Neurochem. 1999;73(3):1090–7.
   Web of Science ®Google Scholar
• Baumann N, Pham-Dinh D. Biology of oligodendrocyte and myelin in the mammalian central nervous system. Physiol Rev. 2001;81(2):871–927.
   PubMed Web of Science ®Google Scholar
• Liu Z, Hu X, Cai J, Liu B, Peng X, Wegner M, et al.. Induction of oligodendrocyte differentiation by Olig2 and Sox10: evidence for reciprocal interactions and dosage-dependent mechanisms. Dev Biol. 2007;302(2):683–93.
   PubMed Web of Science ®Google Scholar
• Norkute A, Hieble A, Braun A, Johann S, Clarner T, Baumgartner W, et al.. Cuprizone treatment induces demyelination and astrocytosis in the mouse hippocampus. J Neurosci Res. 2009;87(6):1343–55.
   PubMed Web of Science ®Google Scholar
• Sim FJ, Hinks GL, Franklin RJ. The re-expression of the homeodomain transcription factor Gtx during remyelination of experimentally induced demyelinating lesions in young and old rat brain. Neuroscience. 2000;100(1):131–9.
   PubMed Web of Science ®Google Scholar
• Goudarzvand M, Javan M, Mirnajafi-Zadeh J, Mozafari S, Tiraihi T. Vitamins E and D3 attenuate demyelination and potentiate remyelination processes of hippocampal formation of rats following local injection of ethidium bromide. Cell Mol Neurobiol. 2010;30(2):289–99.
   PubMed Web of Science ®Google Scholar
• Sherafat MA, Heibatollahi M, Mongabadi S, Moradi F, Javan M, Ahmadiani A. Electromagnetic field stimulation potentiates endogenous myelin repair by recruiting subventricular neural stem cells in an experimental model of white matter demyelination. J Mol Neurosci. 2012;48(1):144–53.
   PubMed Web of Science ®Google Scholar
• Sherafat MA, Javan M, Mozafari S, Mirnajafi-Zadeh J, Motamedi F. Castration attenuates myelin repair following lysolecithin induced demyelination in rat optic chiasm: an evaluation using visual evoked potential, marker genes expression and myelin staining. Neurochem Res. 2011;36(10):1887–95.
   PubMed Web of Science ®Google Scholar
• Franklin RJ, Gilson JM, Blakemore WF. Local recruitment of remyelinating cells in the repair of demyelination in the central nervous system. J Neurosci Res. 1997;50(2):337–44.
   PubMed Web of Science ®Google Scholar
• Sim FJ, Zhao C, Penderis J, Franklin RJ. The age-related decrease in CNS remyelination efficiency is attributable to an impairment of both oligodendrocyte progenitor recruitment and differentiation. J Neurosci. 2002;22(7):2451–9.
   PubMed Web of Science ®Google Scholar
• Buffo A, Vosko MR, Erturk D, Hamann GF, Jucker M, Rowitch D, et al.. Expression pattern of the transcription factor Olig2 in response to brain injuries: implications for neuronal repair. Proc Natl Acad Sci U S A. 2005;102(50):18183–8.
   PubMed Web of Science ®Google Scholar
• Dubois-Dalcq M, Ffrench-Constant C, Franklin RJ. Enhancing central nervous system remyelination in multiple sclerosis. Neuron. 2005;48(1):9–12.
   PubMed Web of Science ®Google Scholar