AMPA receptor: Difference between revisions

From The School of Biomedical Sciences Wiki
Jump to navigation Jump to search
No edit summary
150015248 (talk | contribs)
No edit summary
 
(One intermediate revision by one other user not shown)
Line 1: Line 1:
AMPA receptors are [[Ligand-gated_ion_channel|Ligand gated ion channels]] .The ligand (signalling molecule) they are complementary to is a[[Glutamate|Glutamate]] which is the main excitatory[[Neurotransmitter|neurotransmitter]] in the[[Central_nervous_system|CNS]], this means there is a high proportion of these AMPA receptors on postsynaptic neurons in the brain.<br>When Glutamate binds to AMPA receptors it causes a conformational change and the ion channel opens allowing Na+ ions to flood into the postsynaptic cell. The increase in Na+ concentration causes depolarisation of the postsynaptic membrane generating an[[EPSP|EPSP]] ( which if strong enough can go on to initiate an [[Action_potential|action potential]] at the axon hillock). Repetitive stimulation of these synapses in the brain can cause LTP [[Long_term_potentiation|(Long-term potentiation]]) , due to more Glutamate being released across the synaptic cleft binding to more AMPA receptors which leads to a higher influx of Na+ ions into the cell generating a stronger EPSP. This strong depolarisation of the post-synaptic member aids to the activation of [[NMDA_receptor|NMDA receptors]] ( along with glutamate binding) which allow Ca2+ ions to enter the post synaptic cell. This increase in Ca 2+ concentration can cause new AMPA receptors to be inserted in to the post-synaptic membrane increasing the sensitivity of the post-synaptic cell to Glutamate. <ref>Bruce Alberts, e. a., 2008. Molecular Biology of the cell. 5th ed (pg 690). New York: Garland Science.</ref><br>
AMPA receptors are [[Ligand-gated ion channel|Ligand gated ion channels]].The ligand (signalling molecule) they are complementary to is a [[Glutamate|Glutamate]] which is the main excitatory&nbsp;[[Neurotransmitter|neurotransmitter]] in the&nbsp;[[Central nervous system|CNS]], this means there is a high proportion of these AMPA receptors on postsynaptic neurons in the brain.  


<u>'''References'''</u>
When Glutamate binds to AMPA receptors it causes a conformational change and the ion channel opens allowing Na<sup>+</sup> ions to flood into the postsynaptic cell. The increase in Na<sup>+</sup> concentration causes depolarisation of the postsynaptic membrane generating an&nbsp;[[EPSP|EPSP]] ( which if strong enough can go on to initiate an [[Action potential|action potential]] at the axon hillock). Repetitive stimulation of these synapses in the brain can cause LTP [[Long term potentiation|(Long-term potentiation]]) , due to more Glutamate being released across the synaptic cleft binding to more AMPA receptors which leads to a higher influx of Na<sup>+</sup> ions into the cell generating a stronger EPSP. This strong [[Depolarisation|depolarisation]] of the post-synaptic member aids to the activation of [[NMDA receptor|NMDA receptors]] (along with glutamate binding) which allow Ca<sup>2+</sup> ions to enter the post synaptic cell. This increase in Ca<sup>2+</sup> concentration can cause new AMPA receptors to be inserted in to the post-synaptic membrane increasing the sensitivity of the post-synaptic cell to Glutamate&nbsp;<ref>Bruce Alberts, e. a., 2008. Molecular Biology of the cell. 5th ed (pg 690). New York: Garland Science.</ref>.<br>  


<u</u><references />
=== References  ===
 
<references />

Latest revision as of 12:59, 20 October 2015

AMPA receptors are Ligand gated ion channels.The ligand (signalling molecule) they are complementary to is a Glutamate which is the main excitatory neurotransmitter in the CNS, this means there is a high proportion of these AMPA receptors on postsynaptic neurons in the brain.

When Glutamate binds to AMPA receptors it causes a conformational change and the ion channel opens allowing Na+ ions to flood into the postsynaptic cell. The increase in Na+ concentration causes depolarisation of the postsynaptic membrane generating an EPSP ( which if strong enough can go on to initiate an action potential at the axon hillock). Repetitive stimulation of these synapses in the brain can cause LTP (Long-term potentiation) , due to more Glutamate being released across the synaptic cleft binding to more AMPA receptors which leads to a higher influx of Na+ ions into the cell generating a stronger EPSP. This strong depolarisation of the post-synaptic member aids to the activation of NMDA receptors (along with glutamate binding) which allow Ca2+ ions to enter the post synaptic cell. This increase in Ca2+ concentration can cause new AMPA receptors to be inserted in to the post-synaptic membrane increasing the sensitivity of the post-synaptic cell to Glutamate [1].

References

  1. Bruce Alberts, e. a., 2008. Molecular Biology of the cell. 5th ed (pg 690). New York: Garland Science.