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Related Concept Videos

Chemical Synapses01:26

Chemical Synapses

Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
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 Synapses01:26

Chemical Synapses

Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
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...
Excitatory and Inhibitory Effects of Neurotransmitters01:29

Excitatory and Inhibitory Effects of Neurotransmitters

When an action potential reaches the presynaptic axon terminal, it releases neurotransmitters from the neuron into the synaptic cleft at a chemical synapse. The released neurotransmitter can be excitatory or inhibitory. The critical criteria commonly used to determine whether a molecule is a neurotransmitter at a chemical synapse are the molecule's presence in the presynaptic neuron. Second, its release is in response to strong presynaptic depolarization. And lastly, the presence of specific...
Ligand-Gated Ion Channel Receptor: Gating Mechanism01:30

Ligand-Gated Ion Channel Receptor: Gating Mechanism

Ligand-gated ion channels are transmembrane proteins that play a vital role in intercellular communication and functions of the nervous system. They allow the influx of ions across the membrane once the neurotransmitter binds, allowing the subsequent transmission of electrical excitation across the neurons. Other ligand-gated ion channels, like the γ-aminobutyric acid (GABA) receptor, permit anions like chloride into the cells on the binding of the GABA molecule. Their entry into the cell...
The Synapse02:47

The Synapse

Neurons communicate with one another by passing on their electrical signals to other neurons. A synapse is the location where two neurons meet to exchange signals. At the synapse, the neuron that sends the signal is called the presynaptic cell, while the neuron that receives the message is called the postsynaptic cell. Note that most neurons can be both presynaptic and postsynaptic, as they both transmit and receive information.
Integration of Synaptic Events01:28

Integration of Synaptic Events

Synaptic integration mainly includes the summation of graded potentials. Graded potentials, regardless of their type, cause subtle alterations in membrane voltage, resulting in either depolarization or hyperpolarization. These incremental changes, when combined or summed, can propel the neuron toward its threshold. Consider, for example, a membrane experiencing a +15 mV shift, causing it to depolarize from -70 mV to -55 mV. In this scenario, graded potentials govern the membrane's ability to...

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Related Experiment Video

Updated: Jun 14, 2026

Dopamine Release at Individual Presynaptic Terminals Visualized with FFNs
09:37

Dopamine Release at Individual Presynaptic Terminals Visualized with FFNs

Published on: August 31, 2009

The low synaptic release probability in vivo.

J Gerard G Borst1

  • 1Department of Neuroscience, Erasmus MC, University Medical Center Rotterdam, 3015 GE Rotterdam, The Netherlands. g.borst@erasmusmc.nl

Trends in Neurosciences
|April 8, 2010
PubMed
Summary
This summary is machine-generated.

Synaptic release probability is much lower in vivo than in vitro. This difference in neurotransmitter release may be due to factors like maturation, spontaneous activity, calcium levels, and tonic inhibition.

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Acute Dissociation of Lamprey Reticulospinal Axons to Enable Recording from the Release Face Membrane of Individual Functional Presynaptic Terminals
12:01

Acute Dissociation of Lamprey Reticulospinal Axons to Enable Recording from the Release Face Membrane of Individual Functional Presynaptic Terminals

Published on: October 1, 2014

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Area of Science:

  • Neuroscience
  • Cellular Biology
  • Neurophysiology

Background:

  • Synaptic release probability (SRP) is critical for neural communication.
  • In vitro studies suggest high SRP (around 0.5), but in vivo data implies lower values.

Purpose of the Study:

  • To investigate the discrepancy in SRP measurements between in vitro and in vivo conditions.
  • To understand the physiological regulation of neurotransmitter release at synapses.

Main Methods:

  • Comparison of synaptic potential characteristics in cultured neurons/slices versus in vivo recordings.
  • Analysis of factors potentially influencing SRP in vivo.

Main Results:

  • In vivo synaptic potentials show less dependence on recent activity, indicating lower SRP.
  • Discrepancies may stem from maturational differences, higher spontaneous activity, lower extracellular calcium, and tonic inhibition in vivo.

Conclusions:

  • Presynaptic action potentials trigger neurotransmitter release less frequently in vivo under physiological conditions.
  • In vitro preparations may overestimate synaptic release probability compared to the in vivo environment.