Long-term potentiation is associated with changes in synaptic ultrastructure in the rat neocortex

Synapse ◽  
2006 ◽  
Vol 59 (6) ◽  
pp. 378-382 ◽  
Author(s):  
S. Connor ◽  
P.T.J. Williams ◽  
B. Armstrong ◽  
T.L. Petit ◽  
T.L. Ivanco ◽  
...  
2007 ◽  
Vol 97 (4) ◽  
pp. 2965-2975 ◽  
Author(s):  
Neil R. Hardingham ◽  
Giles E. Hardingham ◽  
Kevin D. Fox ◽  
Julian J. B. Jack

Paired neuronal activity is known to induce changes in synaptic strength that result in the synapse in question having different properties to unmodified synapses. Here we show that in layer 2/3 excitatory connections in young adult rat cortex paired activity acts to normalize the strength and quantal parameters of connections. Paired action potential firing produces long-term potentiation in only a third of connections, whereas a third remain with their amplitude unchanged and a third exhibit long-term depression. Furthermore, the direction of plasticity can be predicted by the initial strength of the connection: weak connections potentiate and strong connections depress. A quantal analysis reveals that changes in synaptic efficacy were predominantly presynaptic in locus and that the key determinant of the direction and magnitude of synaptic modification was the initial release probability ( Pr) of the synapse, which correlated inversely with change in Pr after pairing. Furthermore, distal synapses also exhibited larger potentiations including postsynaptic increases in efficacy, whereas more proximal inputs did not. This may represent a means by which distal synapses preferentially increase their efficacy to achieve equal weighting at the soma. Paired activity thus acts to normalize synaptic strength, by both pre- and postsynaptic mechanisms.


2020 ◽  
Author(s):  
Marta Orlando ◽  
Anton Dvorzhak ◽  
Felicitas Bruentgens ◽  
Marta Maglione ◽  
Benjamin R. Rost ◽  
...  

ABSTRACTSynaptic plasticity is a cellular model for learning and memory. However, the expression mechanisms underlying presynaptic forms of plasticity are not well understood. Here, we investigate functional and structural correlates of long-term potentiation at large hippocampal mossy fiber boutons induced by the adenylyl cyclase activator forskolin. We performed two-photon imaging of the genetically encoded glutamate sensor iGluu that revealed an increase in the surface area used for glutamate release at potentiated terminals. Moreover, time-gated stimulated emission depletion microscopy revealed no change in the coupling distance between immunofluorescence signals from calcium channels and release sites. Finally, by high-pressure freezing and transmission electron microscopy analysis, we found a fast remodeling of synaptic ultrastructure at potentiated boutons: synaptic vesicles dispersed in the terminal and accumulated at the active zones, while active zone density and synaptic complexity increased. We suggest that these rapid and early structural rearrangements likely enable long-term increase in synaptic strength.


1990 ◽  
Vol 530 (1) ◽  
pp. 142-146 ◽  
Author(s):  
Andrius Baskys ◽  
James N. Reynolds ◽  
Peter L. Carlen

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