Related Experiment Video
Updated: Jul 19, 2026

Dopamine Release at Individual Presynaptic Terminals Visualized with FFNs
Published on: August 31, 2009
Ryanodine receptor-transmitter release site coupling increases quantal size in a synapse-specific manner
1Hotchkiss Brain Institute, Department of Cell Biology and Anatomy, Faculty of Medicine, University of Calgary, 3330 Hospital Drive, NW, Calgary, Alberta T2N4N1, Canada.
Presynaptic neurons control synaptic strength by coupling release sites, which multiplies quantal size. This novel mechanism allows differential regulation of synaptic transmission to multiple postsynaptic targets.
Area of Science:
- Neuroscience
- Cellular Biology
- Synaptic Transmission
Background:
- Understanding how presynaptic neurons regulate synaptic transmission to diverse postsynaptic targets is crucial.
- Existing knowledge on differential synaptic regulation is incomplete.
Purpose of the Study:
- To investigate the presynaptic mechanisms underlying differential regulation of synaptic transmission.
- To identify how quantal size is modulated at synapses with multiple postsynaptic cells.
Main Methods:
- Intracellular sharp electrode recordings in identified Lymnaea neurons.
- Whole-cell voltage-clamp recordings of soma-soma synapses.
- Analysis of quantal size and release site coupling.
Main Results:
- Quantal size is presynaptically regulated via the coupling of multiple release sites.
- This coupling effectively multiplies quantal size, influencing synaptic transmission parameters.
- Variation in coupling degree depends on the postsynaptic cell identity, despite presynaptic origin of quantal size variation.
Conclusions:
- A novel presynaptic mechanism for differential regulation of quantal size at specific synaptic connections has been identified.
- Presynaptic neurons can modulate synaptic transmission to multiple postsynaptic cells through this mechanism.
Related Concept Videos
Ligand-Gated Ion Channel Receptor: Gating Mechanism
Neurochemical Transmission: Sites of Drug Action
The Two-State Receptor Model
The binding affinity of a drug determines its interaction with one...
Spare Receptors
Chemical Synapses
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
Chemical Synapses
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...

