Why is magnesium an NMDA antagonist?

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In summary, the NMDA receptor is a ligand gated non-selective cation channel that allows Na+, Ca2+, and K+ to pass through. However, the smallest charge 2 ion, Mg2+, is able to clog up the pore and deactivate the protein, while larger ions like Ca2+ do not have the same effect. This could be due to Mg2+ being more reactive and having a smaller size-charge ratio. Additionally, NMDA receptors are partially voltage gated, which could also play a role in why Mg2+ is able to block the channel.
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mycotheology
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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.
 
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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.
 

1. Why is magnesium considered an NMDA antagonist?

Magnesium is considered an NMDA antagonist because it blocks the NMDA receptor, which is a type of glutamate receptor in the brain. This receptor is responsible for regulating neuronal communication and plays a role in learning and memory. By blocking this receptor, magnesium can reduce the activity of NMDA and prevent excessive activation, which can lead to neuronal damage and excitotoxicity.

2. How does magnesium act as an NMDA antagonist?

Magnesium acts as an NMDA antagonist by binding to specific sites on the NMDA receptor, known as the magnesium binding site. This binding blocks the channel of the receptor, preventing the influx of calcium ions into the neuron. This, in turn, reduces the excitability of the neuron and dampens the transmission of nerve signals.

3. What are the effects of magnesium as an NMDA antagonist?

The effects of magnesium as an NMDA antagonist include reducing the activity of NMDA receptors, which can lead to a decrease in neuronal excitability. This can help prevent excessive glutamate signaling and protect against excitotoxicity, which can damage neurons. Additionally, magnesium can also have anti-inflammatory and neuroprotective effects.

4. What conditions or diseases can benefit from magnesium as an NMDA antagonist?

Magnesium as an NMDA antagonist has shown potential in treating various conditions and diseases, including epilepsy, stroke, traumatic brain injury, and chronic pain. It may also have a role in managing psychiatric disorders such as depression, anxiety, and schizophrenia, which have been linked to NMDA receptor dysfunction.

5. Are there any side effects of magnesium as an NMDA antagonist?

While magnesium is generally considered safe, excessive intake can lead to side effects such as diarrhea, nausea, and abdominal cramps. In rare cases, high doses of magnesium may also cause low blood pressure and irregular heartbeat. It is essential to consult with a healthcare professional before using magnesium as an NMDA antagonist or any other type of medication.

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