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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...
Synaptic Signaling01:09

Synaptic Signaling

Neurons communicate at synapses, or junctions, to excite or inhibit the activity of other neurons or target cells, such as muscles. Synapses may be chemical or electrical.
Most synapses are chemical, meaning an electrical impulse or action potential spurs the release of chemical messengers called neurotransmitters. The neuron sending the signal is called the presynaptic neuron, and the neuron receiving the signal is the postsynaptic neuron.
The presynaptic neuron fires an action potential that...
Synaptic Signaling01:12

Synaptic Signaling

Neurons communicate at synapses, or junctions, to excite or inhibit the activity of other neurons or target cells, such as muscles. Synapses may be chemical or electrical.
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 Role of Ion Channels in Neuronal Computation01:19

The Role of Ion Channels in Neuronal Computation

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.

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Related Experiment Video

Updated: Jun 27, 2026

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

Spine neck plasticity controls postsynaptic calcium signals through electrical compartmentalization.

Asa Grunditz1, Niklaus Holbro, Lei Tian

  • 1Friedrich Miescher Institute, Maulbeerstrasse 66, CH-4058 Basel, Switzerland.

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|December 17, 2008
PubMed
Summary

Dendritic spines dynamically regulate electrical compartmentalization. Spine neck resistance increases with depolarization, enhancing calcium influx crucial for synaptic plasticity.

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

Published on: November 29, 2012

Area of Science:

  • Neuroscience
  • Cellular biology
  • Synaptic plasticity

Background:

  • Dendritic spines are proposed as electrical compartments for local synaptic signal processing.
  • Previous estimates suggested insufficient electrical decoupling between spine heads and parent dendrites.

Purpose of the Study:

  • To investigate the dynamic regulation of electrical compartmentalization in dendritic spines.
  • To understand the role of spine necks in controlling local depolarization and calcium influx.

Main Methods:

  • Experiments conducted in acute hippocampal slices.
  • Utilized N-methyl-D-aspartate (NMDA) receptors as voltage sensors.
  • Measured electrical coupling and calcium influx under varying postsynaptic depolarization levels.

Main Results:

  • Spine compartmentalization was initially weak but increased significantly upon postsynaptic depolarization.
  • Spine necks were found to regulate both diffusional coupling and local spine head depolarization.
  • High-resistance spine necks facilitated calcium influx via NMDA receptors and R-type calcium channels with presynaptic activity alone.

Conclusions:

  • Spine neck plasticity dynamically regulates electrical compartmentalization.
  • This dynamic process controls calcium influx into spines, a critical mechanism for synaptic plasticity.