Literature DB >> 10779547

Inhibition of calcium/calmodulin kinase II alpha subunit expression results in epileptiform activity in cultured hippocampal neurons.

S B Churn1, S Sombati, E R Jakoi, L Severt, R J DeLorenzo, L Sievert.   

Abstract

Several models that develop epileptiform discharges and epilepsy have been associated with a decrease in the activity of calmodulin-dependent kinase II. However, none of these studies has demonstrated a causal relationship between a decrease in calcium/calmodulin kinase II activity and the development of seizure activity. The present study was conducted to determine the effect of directly reducing calcium/calmodulin-dependent kinase activity on the development of epileptiform discharges in hippocampal neurons in culture. Complimentary oligonucleotides specific for the alpha subunit of the calcium/calmodulin kinase were used to decrease the expression of the enzyme. Reduction in kinase expression was confirmed by Western analysis, immunocytochemistry, and exogenous substrate phosphorylation. Increased neuronal excitability and frank epileptiform discharges were observed after a significant reduction in calmodulin kinase II expression. The epileptiform activity was a synchronous event and was not caused by random neuronal firing. Furthermore, the magnitude of decreased kinase expression correlated with the increased neuronal excitability. The data suggest that decreased calmodulin kinase II activity may play a role in epileptogenesis and the long-term plasticity changes associated with the development of pathological seizure activity and epilepsy.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10779547      PMCID: PMC25875          DOI: 10.1073/pnas.080071697

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  30 in total

Review 1.  Calmodulin and protein phosphorylation: implications in brain ischemia.

Authors:  J H Chin; T M Buckholz; R J DeLorenzo
Journal:  Prog Brain Res       Date:  1985       Impact factor: 2.453

2.  Further observations on hippocampal neurons in dispersed cell culture.

Authors:  G A Banker; W M Cowan
Journal:  J Comp Neurol       Date:  1979-10-01       Impact factor: 3.215

3.  Kindling induces a long-lasting change in the activity of a hippocampal membrane calmodulin-dependent protein kinase system.

Authors:  J R Goldenring; C G Wasterlain; A B Oestreicher; P N de Graan; D B Farber; G Glaser; R J DeLorenzo
Journal:  Brain Res       Date:  1986-07-02       Impact factor: 3.252

4.  Identification of the major postsynaptic density protein as homologous with the major calmodulin-binding subunit of a calmodulin-dependent protein kinase.

Authors:  J R Goldenring; J S McGuire; R J DeLorenzo
Journal:  J Neurochem       Date:  1984-04       Impact factor: 5.372

5.  Regional distribution of type II Ca2+/calmodulin-dependent protein kinase in rat brain.

Authors:  N E Erondu; M B Kennedy
Journal:  J Neurosci       Date:  1985-12       Impact factor: 6.167

6.  Evidence that the major postsynaptic density protein is a component of a Ca2+/calmodulin-dependent protein kinase.

Authors:  P T Kelly; T L McGuinness; P Greengard
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

7.  Status epilepticus results in an N-methyl-D-aspartate receptor-dependent inhibition of Ca2+/calmodulin-dependent kinase II activity in the rat.

Authors:  L D Kochan; S B Churn; O Omojokun; A Rice; R J DeLorenzo
Journal:  Neuroscience       Date:  2000       Impact factor: 3.590

8.  Kindling alters the calcium/calmodulin-dependent phosphorylation of synaptic plasma membrane proteins in rat hippocampus.

Authors:  C G Wasterlain; D B Farber
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

9.  Calmodulin systems in neuronal excitability: a molecular approach to epilepsy.

Authors:  R J DeLorenzo
Journal:  Ann Neurol       Date:  1984       Impact factor: 10.422

10.  Decreased calmodulin kinase activity after status epilepticus.

Authors:  J Bronstein; D Farber; C Wasterlain
Journal:  Neurochem Res       Date:  1988-01       Impact factor: 3.996

View more
  18 in total

1.  Distinct terminal and cell body mechanisms in the nociceptor mediate hyperalgesic priming.

Authors:  Luiz F Ferrari; Dioneia Araldi; Jon D Levine
Journal:  J Neurosci       Date:  2015-04-15       Impact factor: 6.167

2.  Hypoxia results in GABAergic channelopathy.

Authors:  Nicholas P Poolos
Journal:  Epilepsy Curr       Date:  2005 Nov-Dec       Impact factor: 7.500

Review 3.  Development of the calcium plateau following status epilepticus: role of calcium in epileptogenesis.

Authors:  Nisha Nagarkatti; Laxmikant S Deshpande; Robert J DeLorenzo
Journal:  Expert Rev Neurother       Date:  2009-06       Impact factor: 4.618

4.  Second messengers mediating the expression of neuroplasticity in a model of chronic pain in the rat.

Authors:  Luiz F Ferrari; Oliver Bogen; Jon D Levine
Journal:  J Pain       Date:  2014-01-07       Impact factor: 5.820

5.  Role of nociceptor αCaMKII in transition from acute to chronic pain (hyperalgesic priming) in male and female rats.

Authors:  Luiz F Ferrari; Oliver Bogen; Jon D Levine
Journal:  J Neurosci       Date:  2013-07-03       Impact factor: 6.167

6.  Neuroligin-1 Knockdown Suppresses Seizure Activity by Regulating Neuronal Hyperexcitability.

Authors:  Min Fang; Jin-Lai Wei; Bo Tang; Jing Liu; Ling Chen; Zhao-Hua Tang; Jing Luo; Guo-Jun Chen; Xue-Feng Wang
Journal:  Mol Neurobiol       Date:  2014-11-27       Impact factor: 5.590

7.  The novel antiepileptic drug carisbamate (RWJ 333369) is effective in inhibiting spontaneous recurrent seizure discharges and blocking sustained repetitive firing in cultured hippocampal neurons.

Authors:  Laxmikant S Deshpande; Nisha Nagarkatti; Sompong Sombati; Robert J DeLorenzo
Journal:  Epilepsy Res       Date:  2008-03-18       Impact factor: 3.045

8.  Carisbamate prevents the development and expression of spontaneous recurrent epileptiform discharges and is neuroprotective in cultured hippocampal neurons.

Authors:  Laxmikant S Deshpande; Nisha Nagarkatti; Julie M Ziobro; Sompong Sombati; Robert J DeLorenzo
Journal:  Epilepsia       Date:  2008-05-20       Impact factor: 5.864

9.  Epileptogenesis causes an N-methyl-d-aspartate receptor/Ca2+-dependent decrease in Ca2+/calmodulin-dependent protein kinase II activity in a hippocampal neuronal culture model of spontaneous recurrent epileptiform discharges.

Authors:  Robert E Blair; Sompong Sombati; Severn B Churn; Robert J Delorenzo
Journal:  Eur J Pharmacol       Date:  2008-04-12       Impact factor: 4.432

10.  In vitro status epilepticus but not spontaneous recurrent seizures cause cell death in cultured hippocampal neurons.

Authors:  Laxmikant S Deshpande; Jeffrey K Lou; Ali Mian; Robert E Blair; Sompong Sombati; Robert J DeLorenzo
Journal:  Epilepsy Res       Date:  2007-07       Impact factor: 3.045

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.