Audiogenic seizure can alter N-methyl-D-aspartate receptor subunits NR1, NR2A, NR2B immunoreactivity in epilepsy-prone rat brain
Luo Qiang
Abstract
Luo Qiang
Abstract
Objective: To determine the role of N methyl D aspartate receptor subunits in the pathogenisis of epilepsy. Methods: Immunohistochemistry was used to detect the protein expression of NMDA receptor subunits NR1, NR2A and NR2B in cortex and hippocampus of genetically epilepsy prone rat (P77PMC) after audiogenic seizure. Results: The NR1 subunit immunoreactivity increased time dependently and reached a peak at hour 24 to 48 in cortex, and at hour 4 in hippocampus respectively after audiogenic seizure and the immunoreactivity of NR2A subunit reduced transiently in CA1 of hippocampus, being maximal 4 8 hours after seizure. In cortex, CA3 and dentate gyrus the immuno staining remained unaltered. No alteration of NR2B was observed at the same time. Conclusion: Those changes may contribute to an altered excitability of neuronal network, and also suggest the alteration of NMDA receptor subunits constitusion after audiogenic seizure in P77PMC rat.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective: To determine the role of N methyl D aspartate receptor subunits in the pathogenisis of epilepsy. Methods: Immunohistochemistry was used to detect the protein expression of NMDA receptor subunits NR1, NR2A and NR2B in cortex and hippocampus of genetically epilepsy prone rat (P77PMC) after audiogenic seizure. Results: The NR1 subunit immunoreactivity increased time dependently and reached a peak at hour 24 to 48 in cortex, and at hour 4 in hippocampus respectively after audiogenic seizure and the immunoreactivity of NR2A subunit reduced transiently in CA1 of hippocampus, being maximal 4 8 hours after seizure. In cortex, CA3 and dentate gyrus the immuno staining remained unaltered. No alteration of NR2B was observed at the same time. Conclusion: Those changes may contribute to an altered excitability of neuronal network, and also suggest the alteration of NMDA receptor subunits constitusion after audiogenic seizure in P77PMC rat.
Key concepts: NMDA receptor, Hippocampus, Epilepsy, Dentate gyrus, Protein subunit, Neuroscience, Immunohistochemistry, Receptor