Why is magnesium an NMDA antagonist?

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The NMDA receptor functions as a ligand-gated non-selective cation channel, permitting the passage of Na+, Ca2+, and K+, with Mg2+ known to block the channel. The discussion centers on why Mg2+ can obstruct the channel while Ca2+, which is larger, does not. It is suggested that Mg2+ is smaller and more reactive than Ca2+, potentially deactivating the receptor rather than physically blocking the pore. A cited study indicates that physiological concentrations of magnesium inhibit NMDA responses in a voltage-dependent manner, supporting the idea that the size-charge ratio of magnesium plays a significant role. Additionally, the NMDA receptor's partial voltage-gated nature is acknowledged, further influencing its interaction with ions.
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The NMDA receptor is a ligand gated non selective cation channel. It allows Na+ and to a lesser extent Ca2+ and K+ to pass through. I read that Mg2+ clogs up the pore. Why would Mg2+ block the channel but not Ca2+? Ca2+ is larger so I'd expect that to be more likely to block an ion channel. Is it because Mg2+ is more electronegative than Ca2+?
 
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mycotheology said:
The NMDA receptor is a ligand gated non selective cation channel. It allows Na+ and to a lesser extent Ca2+ and K+ to pass through. I read that Mg2+ clogs up the pore. Why would Mg2+ block the channel but not Ca2+? Ca2+ is larger so I'd expect that to be more likely to block an ion channel. Is it because Mg2+ is more electronegative than Ca2+?

I'd say its because Mg2+ is the smallest charge 2 ion and is more reactive than Ca2+; clogging up the pore might just mean that it deactivates the protein, not actually block the pore, right? Just my opinion, I'm no expert.
 
Heres a quote from an abstract:
Physiological concentrations of magnesium reduce responses to N M D A by blocking the NMDA-associated ionophore in a voltage-dependent manner [2].
deepblue.lib.umich.edu/bitstream/2027.42/28723/1/0000544.pdf

In a voltage dependent manner so what you said must be correct. Magnesiums size-charge ratio is behind it. I read something about NMDA receptors being partially voltage gated.
 
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