Erratum to "Rapid changes in expression of class I and IV histone deacetylases during epileptogenesis in mouse models of temporal lobe epilepsy" [Exp. Neurol. 273 (2015) 92-104] doi:10.1016/j.expneurol.2015.07.026.;Rapid changes in expression of class I and IV histone deacetylases during epileptogenesis in mouse models of temporal lobe epilepsy

Experimental Neurology

Volumn 273, Issue , 2015, Pages 92-104

  Jagirdar, Rohan ^a   Drexel, Meinrad ^a   Kirchmair, Elke ^a   Tasan, Ramon O ^a   Sperk, Günther ^a  

^a INNSBRUCK MEDICAL UNIVERSITY   (Austria)

Author keywords

Epigenetic; Epilepsy; Epileptogenesis; HDAC; Histone acetylation; Intrahippocampal kainic acid; Status epilepticus

Indexed keywords

HISTONE DEACETYLASE 1; HISTONE DEACETYLASE 4; HISTONE H4; KAINIC ACID; MESSENGER RNA; PILOCARPINE; AMINO ACID RECEPTOR STIMULATING AGENT; CONVULSANT AGENT; HDAC5 PROTEIN, MOUSE; HISTONE DEACETYLASE;

ADULT; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; COMPLEX PARTIAL SEIZURE; CONTROLLED STUDY; ELECTROENCEPHALOGRAM; EPILEPTIC STATE; EPILEPTOGENESIS; GLIA CELL; GRANULE CELL; HIPPOCAMPUS; HISTONE ACETYLATION; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PYRAMIDAL NERVE CELL; TELEMETRY; TEMPORAL LOBE EPILEPSY; ANIMAL; C57BL MOUSE; CHEMICALLY INDUCED; DISEASE MODEL; DRUG EFFECTS; ELECTRODE IMPLANT; ELECTROENCEPHALOGRAPHY; ENZYMOLOGY; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; PHYSIOLOGY; TIME; VIDEORECORDING;

ANIMALS; CONVULSANTS; DISEASE MODELS, ANIMAL; ELECTRODES, IMPLANTED; ELECTROENCEPHALOGRAPHY; EPILEPSY, TEMPORAL LOBE; EXCITATORY AMINO ACID AGONISTS; GENE EXPRESSION REGULATION; HISTONE DEACETYLASE 1; HISTONE DEACETYLASES; KAINIC ACID; MALE; MICE; MICE, INBRED C57BL; PILOCARPINE; TELEMETRY; TIME FACTORS; VIDEO RECORDING;

EID: 84939541460     PISSN: 00144886     EISSN: 10902430     Source Type: Journal    
DOI: 10.1016/j.expneurol.2015.12.021     Document Type: Erratum

References (62)

1. Babb T.L., Lieb J.P., Brown W.J., Pretorius J., Crandall P.H. Distribution of pyramidal cell density and hyperexcitability in the epileptic human hippocampal formation. Epilepsia 1984, 25:721-728.
2. Bahari-Javan S., Maddalena A., Kerimoglu C., Wittnam J., Held T., Bahr M., Burkhardt S., Delalle I., Kugler S., Fischer A., Sananbenesi F. HDAC1 regulates fear extinction in mice. J. Neurosci. 2012, 32:5062-5073.
3. Becker A.J., Pitsch J., Sochivko D., Opitz T., Staniek M., Chen C.C., Campbell K.P., Schoch S., Yaari Y., Beck H. Transcriptional upregulation of Cav3.2 mediates epileptogenesis in the pilocarpine model of epilepsy. J. Neurosci. 2008, 28:13341-13353.
4. Bouilleret V., Ridoux V., Depaulis A., Marescaux C., Nehlig A., Le Gal La Salle G. Recurrent seizures and hippocampal sclerosis following intrahippocampal kainate injection in adult mice: electroencephalography, histopathology and synaptic reorganization similar to mesial temporal lobe epilepsy. Neuroscience 1999, 89:717-729.
5. Brill J., Lee M., Zhao S., Fernald R.D., Huguenard J.R. Chronic valproic acid treatment triggers increased neuropeptide y expression and signaling in rat nucleus reticularis thalami. J. Neurosci. 2006, 26:6813-6822.
6. Broide R.S., Redwine J.M., Aftahi N., Young W., Bloom F.E., Winrow C.J. Distribution of histone deacetylases 1-11 in the rat brain. J. Mol. Neurosci. 2007, 31:47-58.
7. Cavalheiro E.A., Santos N.F., Priel M.R. The pilocarpine model of epilepsy in mice. Epilepsia 1996, 37:1015-1019.
8. Chauviere L., Rafrafi N., Thinus-Blanc C., Bartolomei F., Esclapez M., Bernard C. Early deficits in spatial memory and theta rhythm in experimental temporal lobe epilepsy. J. Neurosci. 2009, 29:5402-5410.
9. Chen Y., Xie Y., Wang H., Chen Y. SIRT1 expression and activity are up-regulated in the brain tissue of epileptic patients and rat models. Nan Fang Yi Ke Da Xue Xue Bao 2013, 33:528-532.
10. Chiaruttini C., Sonego M., Baj G., Simonato M., Tongiorgi E. BDNF mRNA splice variants display activity-dependent targeting to distinct hippocampal laminae. Mol. Cell. Neurosci. 2008, 37:11-19.
11. Chuang D.M., Leng Y., Marinova Z., Kim H.J., Chiu C.T. Multiple roles of HDAC inhibition in neurodegenerative conditions. Trends Neurosci. 2009, 32:591-601.
12. Clynen E., Swijsen A., Raijmakers M., Hoogland G., Rigo J.M. Neuropeptides as targets for the development of anticonvulsant drugs. Mol. Neurobiol. 2014, 50:626-646.
13. Dragunow M., Robertson H.A. Kindling stimulation induces c-fos protein(s) in granule cells of the rat dentate gyrus. Nature 1987, 329:441-442.
14. Drexel M., Kirchmair E., Wieselthaler-Holzl A., Preidt A.P., Sperk G. Somatostatin and neuropeptide Y neurons undergo different plasticity in parahippocampal regions in kainic acid-induced epilepsy. J. Neuropathol. Exp. Neurol. 2012, 71:312-329.
15. Drexel M., Preidt A.P., Sperk G. Sequel of spontaneous seizures after kainic acid-induced status epilepticus and associated neuropathological changes in the subiculum and entorhinal cortex. Neuropharmacology 2012, 63:806-817.
16. Drexel M., Kirchmair E., Sperk G. Changes in the expression of GABAA receptor subunit mRNAs in parahippocampal areas after kainic acid induced seizures. Front Neural Circuits 2013, 7:142.
17. Dugich-Djordjevic M.M., Tocco G., Lapchak P.A., Pasinetti G.M., Najm I., Baudry M., Hefti F. Regionally specific and rapid increases in brain-derived neurotrophic factor messenger RNA in the adult rat brain following seizures induced by systemic administration of kainic acid. Neuroscience 1992, 47:303-315.
18. Esclapez M., Houser C.R. Up-regulation of GAD65 and GAD67 in remaining hippocampal GABA neurons in a model of temporal lobe epilepsy. J. Comp. Neurol. 1999, 412:488-505.
19. Fisher P.D., Sperber E.F., Moshe S.L. Hippocampal sclerosis revisited. Brain Dev. 1998, 20:563-573.
20. Forstermann U., Heldt R., Knappen F., Hertting G. Potential anticonvulsive properties of endogenous prostaglandins formed in mouse brain. Brain Res. 1982, 240:303-310.
21. Franklin K.B.J., Paxinos G. The Mouse Brain in Stereotaxic Coordinates 2008, Elsevier, Amsterdam.
22. Furtinger S., Pirker S., Czech T., Baumgartner C., Ransmayr G., Sperk G. Plasticity of Y1 and Y2 receptors and neuropeptide Y fibers in patients with temporal lobe epilepsy. J. Neurosci. 2001, 21:5804-5812.
23. Gass P., Herdegen T., Bravo R., Kiessling M. Induction of immediate early gene encoded proteins in the rat hippocampus after bicuculline-induced seizures: differential expression of KROX-24, FOS and JUN proteins. Neuroscience 1992, 48:315-324.
24. Gorter J.A., van Vliet E.A., Aronica E., Breit T., Rauwerda H., Lopes da Silva F.H., Wadman W.J. Potential new antiepileptogenic targets indicated by microarray analysis in a rat model for temporal lobe epilepsy. J. Neurosci. 2006, 26:11083-11110.
25. Grooms S.Y., Opitz T., Bennett M.V., Zukin R.S. Status epilepticus decreases glutamate receptor 2 mRNA and protein expression in hippocampal pyramidal cells before neuronal death. Proc. Natl. Acad. Sci. U. S. A. 2000, 97:3631-3636.
26. Guan J.S., Haggarty S.J., Giacometti E., Dannenberg J.H., Joseph N., Gao J., Nieland T.J., Zhou Y., Wang X., Mazitschek R., Bradner J.E., DePinho R.A., Jaenisch R., Tsai L.H. HDAC2 negatively regulates memory formation and synaptic plasticity. Nature 2009, 459:55-60.
27. Haas C.A., Dudeck O., Kirsch M., Huszka C., Kann G., Pollak S., Zentner J., Frotscher M. Role for reelin in the development of granule cell dispersion in temporal lobe epilepsy. J. Neurosci. 2002, 22:5797-5802.
28. Holliday R., Pugh J.E. DNA modification mechanisms and gene activity during development. Science 1975, 187:226-232.
29. Houser C.R. Granule cell dispersion in the dentate gyrus of humans with temporal lobe epilepsy. Brain Res. 1990, 535:195-204.
30. Huang Y., Doherty J.J., Dingledine R. Altered histone acetylation at glutamate receptor 2 and brain-derived neurotrophic factor genes is an early event triggered by status epilepticus. J. Neurosci. 2002, 22:8422-8428.
31. Huang Y., Zhao F., Wang L., Yin H., Zhou C., Wang X. Increased expression of histone deacetylases 2 in temporal lobe epilepsy: a study of epileptic patients and rat models. Synapse 2012, 66:151-159.
32. Hwang J.Y., Aromolaran K.A., Zukin R.S. Epigenetic mechanisms in stroke and epilepsy. Neuropsychopharmacology 2013, 38:167-182.
33. Isackson P.J., Huntsman M.M., Murray K.D., Gall C.M. BDNF mRNA expression is increased in adult rat forebrain after limbic seizures: temporal patterns of induction distinct from NGF. Neuron 1991, 6:937-948.
34. Jones N.C., Kumar G., O'Brien T.J., Morris M.J., Rees S.M., Salzberg M.R. Anxiolytic effects of rapid amygdala kindling, and the influence of early life experience in rats. Behav. Brain Res. 2009, 203:81-87.
35. Khorasanizadeh S., Ostankovitch M. Zooming into epigenetic regulatory elements in health and disease. J. Mol. Biol. 2014, 426:3327-3329.
36. Kimura A., Matsubara K., Horikoshi M. A decade of histone acetylation: marking eukaryotic chromosomes with specific codes. J. Biochem. 2005, 138:647-662.
37. Kobow K., Blumcke I. Epigenetic mechanisms in epilepsy. Prog. Brain Res. 2014, 213:279-316.
38. McClelland S., Flynn C., Dube C., Richichi C., Zha Q., Ghestem A., Esclapez M., Bernard C., Baram T.Z. Neuron-restrictive silencer factor-mediated hyperpolarization-activated cyclic nucleotide gated channelopathy in experimental temporal lobe epilepsy. Ann. Neurol. 2011, 70:454-464.
39. Pallud J., Haussler U., Langlois M., Hamelin S., Devaux B., Deransart C., Depaulis A. Dentate gyrus and hilus transection blocks seizure propagation and granule cell dispersion in a mouse model for mesial temporal lobe epilepsy. Hippocampus 2011, 21:334-343.
40. Peng Z., Huang C.S., Stell B.M., Mody I., Houser C.R. Altered expression of the delta subunit of the GABAA receptor in a mouse model of temporal lobe epilepsy. J. Neurosci. 2004, 24:8629-8639.
41. Pitsch J., Schoch S., Gueler N., Flor P.J., van der Putten H., Becker A.J. Functional role of mGluR1 and mGluR4 in pilocarpine-induced temporal lobe epilepsy. Neurobiol. Dis. 2007, 26:623-633.
42. Rakhade S.N., Jensen F.E. Epileptogenesis in the immature brain: emerging mechanisms. Nat. Rev. Neurol. 2009, 5:380-391.
43. Riban V., Bouilleret V., Pham-Le B.T., Fritschy J.M., Marescaux C., Depaulis A. Evolution of hippocampal epileptic activity during the development of hippocampal sclerosis in a mouse model of temporal lobe epilepsy. Neuroscience 2002, 112:101-111.
44. Schwarzer C., Tsunashima K., Wanzenbock C., Fuchs K., Sieghart W., Sperk G. GABA(A) receptor subunits in the rat hippocampus II: altered distribution in kainic acid-induced temporal lobe epilepsy. Neuroscience 1997, 80:1001-1017.
45. Sharma A.K., Reams R.Y., Jordan W.H., Miller M.A., Thacker H.L., Snyder P.W. Mesial temporal lobe epilepsy: pathogenesis, induced rodent models and lesions. Toxicol. Pathol. 2007, 35:984-999.
46. Simonato M., Tongiorgi E., Kokaia M. Angels and demons: neurotrophic factors and epilepsy. Trends Pharmacol. Sci. 2006, 27:631-638.
47. Sng J.C., Taniura H., Yoneda Y. Inhibition of histone deacetylation by trichostatin A intensifies the transcriptions of neuronal c-fos and c-jun genes after kainate stimulation. Neurosci. Lett. 2005, 386:150-155.
48. Sng J.C., Taniura H., Yoneda Y. Histone modifications in kainate-induced status epilepticus. Eur. J. Neurosci. 2006, 23:1269-1282.
49. Sperk G. Kainic acid seizures in the rat. Prog. Neurobiol. 1994, 42:1-32.
50. Sperk G., Lassmann H., Baran H., Kish S.J., Seitelberger F., Hornykiewicz O. Kainic acid induced seizures: neurochemical and histopathological changes. Neuroscience 1983, 10:1301-1315.
51. Sperk G., Marksteiner J., Gruber B., Bellmann R., Mahata M., Ortler M. Functional changes in neuropeptide Y- and somatostatin-containing neurons induced by limbic seizures in the rat. Neuroscience 1992, 50:831-846.
52. Sperk G., Wieselthaler-Holzl A., Pirker S., Tasan R., Strasser S.S., Drexel M., Pifl C., Marschalek J., Ortler M., Trinka E., Heitmair-Wietzorrek K., Ciofi P., Feucht M., Baumgartner C., Czech T. Glutamate decarboxylase 67 is expressed in hippocampal mossy fibers of temporal lobe epilepsy patients. Hippocampus 2012, 22:590-603.
53. Szabo G., Kartarova Z., Hoertnagl B., Somogyi R., Sperk G. Differential regulation of adult and embryonic glutamate decarboxylases in rat dentate granule cells after kainate-induced limbic seizures. Neuroscience 2000, 100:287-295.
54. Timmusk T., Palm K., Metsis M., Reintam T., Paalme V., Saarma M., Persson H. Multiple promoters direct tissue-specific expression of the rat BDNF gene. Neuron 1993, 10:475-489.
55. Tsankova N.M., Kumar A., Nestler E.J. Histone modifications at gene promoter regions in rat hippocampus after acute and chronic electroconvulsive seizures. J. Neurosci. 2004, 24:5603-5610.
56. Tsunashima K., Schwarzer C., Kirchmair E., Sieghart W., Sperk G. GABA(A) receptor subunits in the rat hippocampus III: altered messenger RNA expression in kainic acid-induced epilepsy. Neuroscience 1997, 80:1019-1032.
57. Vezzani A., Sperk G. Overexpression of NPY and Y2 receptors in epileptic brain tissue: an endogenous neuroprotective mechanism in temporal lobe epilepsy?. Neuropeptides 2004, 38:245-252.
58. Vezzani A., French J., Bartfai T., Baram T.Z. The role of inflammation in epilepsy. Nat. Rev. Neurol. 2011, 7:31-40.
59. Voelter-Mahlknecht S., Ho A.D., Mahlknecht U. Chromosomal organization and localization of the novel class IV human histone deacetylase 11 gene. Int. J. Mol. Med. 2005, 16:589-598.
60. Wasterlain C.G. Breakdown of brain polysomes in status epilepticus. Brain Res. 1972, 39:278-284.
61. Williams P.A., White A.M., Clark S., Ferraro D.J., Swiercz W., Staley K.J., Dudek F.E. Development of spontaneous recurrent seizures after kainate-induced status epilepticus. J. Neurosci. 2009, 29:2103-2112.
62. Yao Z.G., Zhang L., Huang L., Zhu H., Liu Y., Ma C.M., Sheng S.L., Qin C. Regional and cell-type specific distribution of HDAC2 in the adult mouse brain. Brain Struct. Funct. 2013, 218:563-573.