scholarly journals Vesicular Glutamate Transporter VGLUT1 Has a Role in Hippocampal Long-Term Potentiation and Spatial Reversal Learning

2009 ◽  
Vol 20 (3) ◽  
pp. 684-693 ◽  
Author(s):  
D. Balschun ◽  
D. Moechars ◽  
Z. Callaerts-Vegh ◽  
B. Vermaercke ◽  
N. Van Acker ◽  
...  
Keyword(s):  
Reversal Learning ◽  
Glutamate Transporter ◽  
Long Term Potentiation ◽  
Vesicular Glutamate Transporter ◽  
Spatial Reversal ◽  
Term Potentiation

scholarly journals Expression mechanisms underlying long-term potentiation: a postsynaptic view

2003 ◽  
Vol 358 (1432) ◽  
pp. 721-726 ◽  
Author(s):  
Roger A. Nicoll
Keyword(s):  
Nmda Receptor ◽  
Ampa Receptors ◽  
Glutamate Release ◽  
Glutamate Transporter ◽  
Long Term Potentiation ◽  
Receptor Activation ◽  
Covalent Modification ◽  
Term Potentiation ◽  
Expression Mechanism

This review summarizes the various experiments that have been carried out to determine if the expression of long-term potentiation (LTP), in particular N -methyl-D-aspartate (NMDA) receptor-dependent LTP, is presynaptic or postsynaptic. Evidence for a presynaptic expression mechanism comes primarily from experiments reporting that glutamate overflow is increased during LTP and from experiments showing that the failure rate decreases during LTP. However, other experimental approaches, such as monitoring synaptic glutamate release by recording astrocytic glutamate transporter currents, have failed to detect any change in glutamate release during LTP. In addition, the discovery of silent synapses, in which LTP rapidly switches on α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor function at NMDA-receptor-only synapses, provides a postsynaptic mechanism for the decrease in failures during LTP. It is argued that the preponderance of evidence favours a postsynaptic expression mechanism, whereby NMDA receptor activation results in the rapid recruitment of AMPA receptors as well as a covalent modification of synaptic AMPA receptors.

scholarly journals Differences in GluN2B-containing NMDA receptors result in opposite long-term plasticity and dopaminergic modulation at ipsilateral vs. contralateral cortico-striatal synapses

2019 ◽  
Author(s):  
Wei Li ◽  
Lucas Pozzo-Miller
Keyword(s):  
Synaptic Plasticity ◽  
Primary Motor Cortex ◽  
Glutamate Transporter ◽  
Long Term Potentiation ◽  
D1 Receptors ◽  
Synaptic Structure ◽  
Term Potentiation ◽  
Nmdar Subunit ◽  
And Function

AbstractExcitatory neurons in the primary motor cortex project bilaterally to the striatum. However, whether synaptic structure and function in ipsilateral and contralateral cortico-striatal pathways is identical or different remains largely unknown. Here, we describe that excitatory synapses in the contralateral pathway have higher levels of NMDA-type of glutamate receptors (NMDARs) than those in the ipsilateral pathway, although both synapses utilize the same presynaptic vesicular glutamate transporter. We also show that NMDARs containing the GluN2B subunit, but not GluN2A, contribute to this difference. The altered NMDAR subunit composition in these two pathways results in opposite synaptic plasticity: long-term depression in the ipsilateral pathway and long-term potentiation in the contralateral pathway. Furthermore, we demonstrate that activation of D1 and D2 dopamine (DA) receptors by either selective pharmacological agonists or light-induced release of endogenous DA have no effect on NMDAR-mediated neurotransmission in either pathway. However, blocking basal DAergic tone with either D1 or D2 with selective antagonists revealed that GluN2B-containing NMDARs are modulated by D1 receptors in the contralateral pathway and by D2 receptors in the ipsilateral pathway. Such distinct modulatory actions seem to be permissive rather than sufficient for the induction of long-term synaptic plasticity. Altogether, our results provide novel and unexpected evidence for the lack of bilaterality of NMDAR-mediated synaptic transmission at cortico-striatal pathways due to differences in the expression of GluN2B subunits, which results in differences in bidirectional synaptic plasticity and modulation by dopaminergic inputs.

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