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Published on: August 14, 2015
Inhibition of calcium/calmodulin kinase II alpha subunit expression results in epileptiform activity in cultured
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.
Insights
Decreasing calcium/calmodulin kinase II activity in hippocampal neurons directly caused increased neuronal excitability and epileptiform discharges, suggesting a causal role in epilepsy development.
Area of Science:
- Neuroscience
- Cellular Biology
- Epilepsy Research
Background:
- Previous models linked decreased calmodulin-dependent kinase II activity to epilepsy.
- A direct causal link between reduced kinase activity and seizure development remained unproven.
Purpose of the Study:
- To determine if reducing calcium/calmodulin-dependent kinase II activity directly causes epileptiform discharges.
- To investigate the role of this kinase in epileptogenesis.
Main Methods:
- Used complementary oligonucleotides to reduce calcium/calmodulin kinase II alpha subunit expression in cultured hippocampal neurons.
- Confirmed reduced kinase expression via Western analysis, immunocytochemistry, and phosphorylation assays.
- Monitored neuronal excitability and discharge patterns.
Main Results:
- Significant reduction in calmodulin kinase II expression led to increased neuronal excitability.
- Frank, synchronous epileptiform discharges were observed.
- A correlation was found between the degree of kinase reduction and increased excitability.
Conclusions:
- Decreased calmodulin kinase II activity may directly contribute to epileptogenesis.
- This reduction could be involved in long-term plasticity changes leading to epilepsy.

