Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Integration of Synaptic Events01:28

Integration of Synaptic Events

4.3K
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...
4.3K
Ligand-Gated Ion Channel Receptor: Gating Mechanism01:30

Ligand-Gated Ion Channel Receptor: Gating Mechanism

4.2K
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...
4.2K
The Role of Ion Channels in Neuronal Computation01:19

The Role of Ion Channels in Neuronal Computation

3.9K
A postsynaptic neuron usually receives numerous impulses from several other presynaptic neurons. The axon hillock of the postsynaptic neuron integrates all these signals and determines the likelihood of firing an action potential.
Sometimes a single EPSP is strong enough to induce an action potential in the postsynaptic neuron. However, multiple presynaptic inputs must often create EPSPs around the same time for the postsynaptic neuron to be sufficiently depolarized to fire an action potential....
3.9K
Chemical Synapses01:26

Chemical Synapses

12.0K
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...
12.0K
Chemical Synapses01:26

Chemical Synapses

4.7K
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...
4.7K
Excitatory and Inhibitory Effects of Neurotransmitters01:29

Excitatory and Inhibitory Effects of Neurotransmitters

13.4K
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...
13.4K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Vectorized instructive signals in cortical dendrites.

Nature·2026
Same author

Plateau potentials are instructive signals for behavioral timescale synaptic plasticity in the neocortex.

bioRxiv : the preprint server for biology·2025
Same author

Patch2MAP combines patch-clamp electrophysiology with super-resolution structural and protein imaging in identified single neurons without genetic modification.

Scientific reports·2025
Same author

Spatial reasoning via recurrent neural dynamics in mouse retrosplenial cortex.

Nature neuroscience·2025
Same author

Silent Synapses in the Adult Brain.

Annual review of neuroscience·2025
Same author

ONIX: a unified open-source platform for multimodal neural recording and perturbation during naturalistic behavior.

Nature methods·2024
Same journal

Spatiomolecular mapping reveals anatomical organization of heterogeneous cell types in the human nucleus accumbens.

Neuron·2026
Same journal

TGF-β1-induced endothelial transcytosis drives blood-brain barrier leakage during aging.

Neuron·2026
Same journal

Image space opens up for visual neuroscience.

Neuron·2026
Same journal

Septal GLP-1 receptors control alcohol taking and seeking.

Neuron·2026
Same journal

Microglial fitness in moderation: Tuning TREM2 signaling through Ptpn6.

Neuron·2026
Same journal

Human astrocytes keep time with inflammation.

Neuron·2026
See all related articles

Related Experiment Video

Updated: Feb 16, 2026

Voltage-sensitive Dye Recording from Axons, Dendrites and Dendritic Spines of Individual Neurons in Brain Slices
12:51

Voltage-sensitive Dye Recording from Axons, Dendrites and Dendritic Spines of Individual Neurons in Brain Slices

Published on: November 29, 2012

17.3K

Dendritic Spines Prevent Synaptic Voltage Clamp.

Lou Beaulieu-Laroche1, Mark T Harnett1

  • 1Department of Brain and Cognitive Sciences, McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

Neuron
|December 19, 2017
PubMed
Summary
This summary is machine-generated.

Voltage clamp is ineffective for studying excitatory synapses due to electrical compartmentalization. New methods reveal larger AMPA conductance than previously thought, impacting synaptic current measurements.

More Related Videos

Two-photon Calcium Imaging in Neuronal Dendrites in Brain Slices
10:35

Two-photon Calcium Imaging in Neuronal Dendrites in Brain Slices

Published on: March 15, 2018

11.6K
3D Modeling of Dendritic Spines with Synaptic Plasticity
07:13

3D Modeling of Dendritic Spines with Synaptic Plasticity

Published on: May 18, 2020

7.4K

Related Experiment Videos

Last Updated: Feb 16, 2026

Voltage-sensitive Dye Recording from Axons, Dendrites and Dendritic Spines of Individual Neurons in Brain Slices
12:51

Voltage-sensitive Dye Recording from Axons, Dendrites and Dendritic Spines of Individual Neurons in Brain Slices

Published on: November 29, 2012

17.3K
Two-photon Calcium Imaging in Neuronal Dendrites in Brain Slices
10:35

Two-photon Calcium Imaging in Neuronal Dendrites in Brain Slices

Published on: March 15, 2018

11.6K
3D Modeling of Dendritic Spines with Synaptic Plasticity
07:13

3D Modeling of Dendritic Spines with Synaptic Plasticity

Published on: May 18, 2020

7.4K

Area of Science:

  • Neuroscience
  • Computational Neuroscience
  • Electrophysiology

Background:

  • Synapses are crucial for brain information processing.
  • Voltage-clamp analysis is a primary method for studying synaptic physiology.
  • Existing methods may be limited by electrical properties of neuronal structures.

Purpose of the Study:

  • To investigate the effectiveness of voltage clamp for excitatory synapses.
  • To identify and overcome errors in synaptic measurements caused by electrical compartmentalization.
  • To accurately measure single-synapse AMPA conductance.

Main Methods:

  • Local dendritic voltage clamp application.
  • Analysis of spine head depolarization during single-spine activation.
  • Development of a novel approach for accurate synaptic conductance measurement.

Main Results:

  • Voltage clamp is ineffective for most excitatory synapses due to spine electrical compartmentalization.
  • Single-spine activation causes significant spine head depolarization, distorting measurements.
  • Single-synapse AMPA conductance is substantially larger than previously estimated.
  • Observed larger conductance leads to saturation effects on synaptic currents.

Conclusions:

  • Electrical compartmentalization significantly impacts synaptic function.
  • Standard electrophysiological methods like voltage clamp may yield inaccurate results for synaptic measurements.
  • Accurate assessment of synaptic function requires accounting for electrical compartmentalization.