here's what I think is HY:
1. the NMDA receptor if found throughout the CNS (eg.hippocampus, cerebral cortex, spinal cord)
2. when glutamate n the cofactor glycine bind to the NMDA receptor the gate is opened and influx of Na n Ca and efflux of K occurs.
3. in addition, a voltage dependent membrane depolarization is required to open the gate bcz the NMDA receptor is "plugged" by extracellular Mg at resting membrane potential.
4. drugs, Amantidine (noncompetitive blocker)
Memantine (noncompetitive, use-Dependant blocker)
Ketamine (Ketalar, special K, k) is an antagoinist that acts as a CNS depressent & dissociative anesthetic, date rape drug.
PCP n Dizocilpne are NMDA receptor open channel blockers.
Will add your points as well.
1. the NMDA receptor if found throughout the CNS (eg.hippocampus, cerebral cortex, spinal cord)
2. when glutamate n the cofactor glycine bind to the NMDA receptor the gate is opened and influx of Na n Ca and efflux of K occurs.
3. in addition, a voltage dependent membrane depolarization is required to open the gate bcz the NMDA receptor is "plugged" by extracellular Mg at resting membrane potential.
4. drugs, Amantidine (noncompetitive blocker)
Memantine (noncompetitive, use-Dependant blocker)
Ketamine (Ketalar, special K, k) is an antagoinist that acts as a CNS depressent & dissociative anesthetic, date rape drug.
PCP n Dizocilpne are NMDA receptor open channel blockers.
Will add your points as well.