| Project/Area Number |
04670127
|
|---|
| Research Category |
Grant-in-Aid for General Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Research Field |
General pharmacology
|
|---|
| Research Institution | Kyoto Prefectural University of Medicine |
|---|
Principal Investigator |
OHKUMA Seitaro Kyoto Prof.Univ.of Med., Dept.of Phamacol.Associate Prof., 医学部, 助教授 (30152086)
|
|---|
| Project Period (FY) |
1992 – 1993
|
| Project Status |
Completed (Fiscal Year 1993)
|
| Budget Amount *help |
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1993: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1992: ¥1,300,000 (Direct Cost: ¥1,300,000)
|
|---|
| Keywords | NMDA receptor / neuronal death / GABA_A receptor / ca-channel blocker / NG108-15 cells / Ca influx / [^3H]MK-801 binding / cerebral cortical neurons / NG108-15 |
|---|
| Research Abstract |
In the present study, effect of various neurotransmitter receptors on NMDA-induced neuronal injury was investigated using primary cultured cerebral cortical neurons and whether neuroblastoma x glioma hybrid NG108-15 (NG cells) possess NMDA receptor was also examined. The follwing results were obtained.
1) NG cells showed the response of calcium influx to NMDA receptor stimulation and had the binding sites of [^3H]MK-801, a radiolabeled ligand specific for NMDA receptor, which assumed to be similar to those found in neurons in rodents brain. These results indicate that NG cells possess NMDA receptor with pharmacological property.
2) NMDA dose-dependently induced the leakage of LDH activity from cerebral cortical neurons during 1 hr subsequent to the exposure to NMDA for 15 min. This NMDA-induced leakage of LDH activity was significantly inhibited by GABA_A receptor stimulation, while the stimulation of muscarinic and beta-receptors showed no effects on NMDA-induced leakage of LDH activity.
3)NMDA induced [^<45>Ca]influx into cerebral cortical neurons. Several GABA_A receptor agonists enhanced this NMDA-induced [^<45>Ca]influx. Chloride channel inhibitors functionally coupling to GABA_A receptor such as picrotoxinin and TBPS showed no inhibition, while voltage-dependent calcium channel blockers reduced this stimulatory effects of GABA_A receptor agonists.
|
