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Updated: Aug 19, 2026

Single-Cell Calcium Imaging for Studying the Activation of Calcium Ion Channels
Published on: December 13, 2024
[Dual action of intracellularly released calcium on the quantal mediator secretion]
Abstract:
The mice diaphragm muscle and microelectrode technique were used to check the influence of ryanodine (0.5 mcM) on spontaneous and evoked mediator release under conditions of potassium depolarization (8-16 mM [K+]ex or rhythmic (4-100 Hz) stimulation of motor nerve terminals. Weak tonic calcium loading (by muscle exposition to 8 mM [K+]ex) caused a two-fold frequency increase if miniature and plate potentials (MEPPs), which was returned to the basal level by subsequent application of ryanodine. This inhibitory effect of ryanodine was blocked by apamin (500 nM) a blocker of K+(Ca)-channels. A greater calcium load of terminals (in solution with 16 mM [K+]ex) caused a 15-fold increase of MEPPs frequency. Subsequent ryanodine application caused an additional 2-3-fold increase of MEPPs frequency. During rhythmic activity of motor synapses, ryanodine was able to decrease the amplitude of EPP by 60% at plateau phase at short low frequency (4 Hz) of discharges and to increase the amplitude of EPP by 60-150% at high frequency (70-100 Hz) of discharges. It is concluded that rynodine induced calcium release from intraterminal Ca2+-stores can influence dual: excitatory or inhibitory, action on spontaneous and evoked mediator release, due to different intraterminal calcium loads and regimen of synaptic activity.
Insights
Ryanodine influences neurotransmitter release by affecting calcium stores in nerve terminals. Its effects can be either inhibitory or excitatory depending on calcium levels and nerve activity.
Area of Science:
- Neuroscience
- Molecular Biology
- Muscle Physiology
Background:
- Neurotransmitter release is crucial for synaptic function.
- Intracellular calcium stores play a significant role in regulating neurotransmitter release.
- Ryanodine is known to interact with calcium release channels.
Purpose of the Study:
- To investigate the effect of ryanodine on spontaneous and evoked neurotransmitter release.
- To determine how ryanodine's action is modulated by different calcium loads and stimulation frequencies.
- To elucidate the role of intraterminal calcium stores in synaptic transmission.
Main Methods:
- Experiments conducted on mouse diaphragm muscle using microelectrode techniques.
- Assessment of spontaneous and evoked mediator release under varying potassium-induced depolarization (8-16 mM [K+]ex).
- Evaluation of ryanodine's effects during rhythmic motor nerve terminal stimulation (4-100 Hz).
Main Results:
- Low calcium load increased miniature and plate potentials (MEPPs) frequency, inhibited by ryanodine.
- High calcium load led to a significant increase in MEPPs frequency, further enhanced by ryanodine.
- Ryanodine modulated excitatory postsynaptic potential (EPP) amplitude, decreasing it at low frequencies and increasing it at high frequencies.
Conclusions:
- Ryanodine-induced calcium release from intraterminal stores has a dual effect on neurotransmitter release.
- The action of ryanodine is dependent on the intraterminal calcium load and synaptic activity patterns.
- This highlights the complex role of intracellular calcium dynamics in synaptic transmission.
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