Separating kindling and LTP: Lessons from studies of PKM zeta in developing and adult rats

Neuroscience Letters

Volumn 453, Issue 3, 2009, Pages 229-232

  Heida, James G ^a   Englot, Dario J ^b   Sacktor, Todd C ^c   Blumenfeld, Hal ^b   Moshé, Solomon L ^a  

^a MONTEFIORE MEDICAL CENTER   (United States)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c SUNY Downstate Medical Center   (United States)

Author keywords

Development; Protein kinase; Rat; Seizures

Indexed keywords

PROTEIN KINASE C; PROTEIN KINASE M ZETA; UNCLASSIFIED DRUG;

AMYGDALOID NUCLEUS; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; EPILEPTOGENESIS; HIPPOCAMPUS; KINDLING; LONG TERM POTENTIATION; MALE; MEMORY CONSOLIDATION; NONHUMAN; PRIORITY JOURNAL; RAT;

AGE FACTORS; ANIMALS; ISOENZYMES; KINDLING, NEUROLOGIC; LONG-TERM POTENTIATION; MALE; PEPTIDES; PROTEIN KINASE C; RATS; RATS, SPRAGUE-DAWLEY; SEIZURES;

EID: 62249162152     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2009.02.037     Document Type: Article

References (28)

1. Adams B., Sazgar M., Osehobo P., Van der Zee C.E., Diamond J., Fahnestock M., and Racine R.J. Nerve growth factor accelerates seizure development, enhances mossy fiber sprouting, and attenuates seizure-induced decreases in neuronal density in the kindling model of epilepsy. J. Neurosci. 17 (1997) 5288-5296
2. Albensi B.C., Oliver D.R., Toupin J., and Odero G. Electrical stimulation protocols for hippocampal synaptic plasticity and neuronal hyper-excitability: are they effective or relevant?. Exp. Neurol. 204 (2007) 1-13
3. Bliss T.V.P., and Lømo T. Long-lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path. J. Physiol. 232 (1973) 331-356
4. Blumenfeld H., Rivera M., Vasquez J.G., Shah A., Ismail D., Enev M., and Zaveri H.P. Neocortical and thalamic spread of amygdala kindled seizures. Epilepsia 48 (2007) 254-262
5. Bolkvadze T.A., Dzhaparidze N.D., Zhvaniya M.G., Bikashvili T.Z., and Chilachava L.R. Kindling-induced hippocampal cell death in rats. Neurosci. Behav. Physiol. 38 (2008) 359-362
6. Drier E.A., Tello M.K., Cowan M., Wu P., Blace N., Sacktor T.C., and Yin J.C. Memory enhancement and formation by atypical PKM activity in Drosophila melanogaster. Nat. Neurosci. 5 (2002) 316-324
7. Goddard G.V., McIntyre D.C., and Leech C.K. A permanent change in brain function resulting from daily electrical stimulation. Exp. Neurol. 25 (1969) 295-330
8. Haas K., Sperber E.F., and Moshé S.L. Kindling in developing animals: expression of severe seizures and enhanced development of bilateral foci, Dev. Brain Res. 56 (1990) 275-280
9. Haas K.Z., Sperber E.F., Opanashuk L.A., Stanton P.K., and Moshé S.L. Resistance of immature hippocampus to morphologic and physiologic alterations following status epilepticus or kindling. Hippocampus 11 (2001) 615-625
10. Heida J.G., Teskey G.C., and Pittman Q.J. Febrile convulsions induced by the combination of lipopolysaccharide and low-dose kainic acid enhance seizure susceptibility, not epileptogenesis, in rats. Epilepsia 46 (2005) 1898-1905
11. Holmes G.L. Animal model studies application to human patients. Neurology 69 (2007) S28-S32
12. +)/calmodulin-dependent kinases. J. Physiol. 584 (2007) 885-894
13. Li S., Reinprecht I., Fahnestock M., and Racine R.J. Activity-dependent changes in synaptophysin immunoreactivity in hippocampus, piriform cortex, and entorhinal cortex of the rat. Neuroscience 115 (2002) 1221-1229
14. Lothman E.W., and Williamson J.M. Rapid kindling with recurrent hippocampal seizures. Epilepsy Res. 14 (1993) 209-220
15. McEachern J.C., and Shaw C.A. The plasticity-pathology continuum: defining a role for the LTP phenomenon. J. Neurosci. Res. 58 (1999) 42-61
16. Morimoto K., Fahnestock M., and Racine R.J. Kindling and status epilepticus models of epilepsy: rewiring the brain. Prog. Neurobiol. 73 (2004) 1-60
17. Moshé S.L. The effects of age on the kindling phenomenon. Dev. Psychobiol. 14 (1981) 75-81
18. Nicoll R.A., and Malenka R.C. Expression mechanisms underlying NMDA receptor-dependent long-term potentiation. Ann. N. Y. Acad. Sci. 868 (1999) 515-525
19. Pastalkova E., Serrano P., Pinkhasova D., Wallace E., Fenton A.A., and Sacktor T.C. Storage of spatial information by the maintenance mechanism of LTP. Science 313 (2006) 1141-1144
20. Racine R.J. Modification of seizure activity by electrical stimulation: II. Motor seizures. Electroencephal. Clin. Neurophysiol. 32 (1972) 281-294
21. Sacktor T.C. PKMzeta, LTP maintenance, and the dynamic molecular biology of memory storage, Prog. Brain Res. 169 (2008) 27-40
22. Schubert M., Siegmund H., Pape H.C., and Albrecht D. Kindling-induced changes in plasticity of the rat amygdala and hippocampus. Learn Mem. 12 (2005) 520-526
23. Scott B.W., Wang S., Burnham W.M., De Boni U., and Wojtowicz J.M. Kindling-induced neurogenesis in the dentate gyrus of the rat. Neurosci. Lett. 248 (1998) 73-76
24. Serrano P., Yao Y., and Sacktor T.C. Persistent phosphorylation by protein kinase Mzeta maintains late-phase long-term potentiation. J. Neurosci. 25 (2005) 1979-1984
25. Shema R., Sacktor T.C., and Dudai Y. Rapid erasure of long-term memory associations in the cortex by an inhibitor of PKM zeta. Science 317 (2007) 951-953
26. Soderling T.R., and Derkach V.A. Postsynaptic protein phosphorylation and LTP. Trends Neurosci. 23 (2000) 75-80
27. Teyler T.J., and DiScenna P. The role of hippocampus in memory: a hypothesis. Neurosci. Biobehav. Rev. 9 (1985) 377-389
28. +/calmodulin-dependent protein kinase II in septally kindled rat brains: changes in protein level, activity and subcellular distribution in hippocampus and cerebral cortex. Neurosci. Lett. 211 (1996) 109-112