Abstract

Action potentials arriving at a nerve terminal activate voltage-gated calcium channels and set the electrical driving force for calcium entry which affects the amount and duration of neurotransmitter release. During propagation, the duration, amplitude, and shape of action potentials often changes. This affects calcium entry, and can cause large changes in neurotransmitter release. Here, we have used a series of amplitude and area matched stimuli to examine how the shape and amplitude of a stimulus affect calcium influx at a presynaptic nerve terminal in the mammalian brain. We identify fundamental differences in calcium entry following calcium channel activation by a standard voltage jump vs. an action potential-like stimulation. We also tested a series of action potential-like stimuli with the same amplitude, duration, and stimulus area, but differing in their rise and decay times. We find that a stimulus that matches the rise and decay times of a physiological action potential produces a calcium channel response that is optimized over a range of peak amplitudes. Next, we determined the relative number of calcium channels that are active at different times during an action potential, which is important in the context of how local calcium domains trigger neurotransmitter release. We find the depolarizing phase of an AP-like stimulus only opens ~20% of the maximum number of calcium channels that can be activated. Channels continue to activate during the falling phase of the action potential, with peak calcium channel activation occurring near 0 mV. Although less than 25% of calcium channels are active at the end of the action potential, these calcium channels will generate a larger local calcium concentration that will increase the release probability for nearby vesicles. Determining the change in open probability of presynaptic calcium channels, and taking into account how local calcium concentration also changes throughout the action potential are both necessary to fully understand how the action potential triggers neurotransmitter release.

Highlights

  • Action potential amplitude, duration, and shape can change during repeated activity, with exposure to certain drugs or toxins, as a result of some pathologies, and during propagation

  • To determine if there are basic differences in calcium channel currents generated by voltage jump stimuli vs. stimuli with a ramped depolarization and repolarization, we first tested sets of stimuli with instant voltage jumps at three different peak amplitudes

  • The tail current rapidly decays as calcium channel deactivation occurs in response to the change in membrane potential

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Summary

Introduction

Duration, and shape can change during repeated activity, with exposure to certain drugs or toxins, as a result of some pathologies, and during propagation. The duration, amplitude and the speed of the rising and falling phase of the action potential are controlled by the activation and density of voltage-gated sodium and potassium channels. Since the triggering of neurotransmitter release is highly sensitive to the local presynaptic calcium level (Heidelberger et al, 1994; Augustine, 2001; Neher and Sakaba, 2008) the shape and duration of the action potential and the peak amplitude of the action potential are major determinants of calcium channel activation and calcium entry which determines the amount of synaptic vesicle release (Wu et al, 2004; Yang and Wang, 2006; Hoppa et al, 2014). Several groups have used AP waveforms or AP-like stimuli to study calcium channel activity (McCobb and Beam, 1991; Borst and Sakmann, 1998; Pattillo et al, 1999; Sheng et al, 2012) and neurotransmitter release (Wu et al, 2004; Yang and Wang, 2006)

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