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Transient and Steady-State Properties of Drosophila Sensory Neurons Coding Noxious Cold Temperature

Coding noxious cold signals, such as the magnitude and rate of temperature change, play essential roles in the survival of organisms. We combined electrophysiological and computational neuroscience methods to investigate the neural dynamics of Drosophila larva cold-sensing Class III (CIII) neurons....

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Autores principales: Maksymchuk, Natalia, Sakurai, Akira, Cox, Daniel N., Cymbalyuk, Gennady
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358291/
https://www.ncbi.nlm.nih.gov/pubmed/35959471
http://dx.doi.org/10.3389/fncel.2022.831803
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author Maksymchuk, Natalia
Sakurai, Akira
Cox, Daniel N.
Cymbalyuk, Gennady
author_facet Maksymchuk, Natalia
Sakurai, Akira
Cox, Daniel N.
Cymbalyuk, Gennady
author_sort Maksymchuk, Natalia
collection PubMed
description Coding noxious cold signals, such as the magnitude and rate of temperature change, play essential roles in the survival of organisms. We combined electrophysiological and computational neuroscience methods to investigate the neural dynamics of Drosophila larva cold-sensing Class III (CIII) neurons. In response to a fast temperature change (–2 to –6°C/s) from room temperature to noxious cold, the CIII neurons exhibited a pronounced peak of a spiking rate with subsequent relaxation to a steady-state spiking. The magnitude of the peak was higher for a higher rate of temperature decrease, while slow temperature decrease (–0.1°C/s) evoked no distinct peak of the spiking rate. The rate of the steady-state spiking depended on the magnitude of the final temperature and was higher at lower temperatures. For each neuron, we characterized this dependence by estimating the temperature of the half activation of the spiking rate by curve fitting neuron’s spiking rate responses to a Boltzmann function. We found that neurons had a temperature of the half activation distributed over a wide temperature range. We also found that CIII neurons responded to decrease rather than increase in temperature. There was a significant difference in spiking activity between fast and slow returns from noxious cold to room temperature: The CIII neurons usually stopped activity abruptly in the case of the fast return and continued spiking for some time in the case of the slow return. We developed a biophysical model of CIII neurons using a generalized description of transient receptor potential (TRP) current kinetics with temperature-dependent activation and Ca(2+)-dependent inactivation. This model recapitulated the key features of the spiking rate responses found in experiments and suggested mechanisms explaining the transient and steady-state activity of the CIII neurons at different cold temperatures and rates of their decrease and increase. We conclude that CIII neurons encode at least three types of cold sensory information: the rate of temperature decrease by a peak of the firing rate, the magnitude of cold temperature by the rate of steady spiking activity, and direction of temperature change by spiking activity augmentation or suppression corresponding to temperature decrease and increase, respectively.
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spelling pubmed-93582912022-08-10 Transient and Steady-State Properties of Drosophila Sensory Neurons Coding Noxious Cold Temperature Maksymchuk, Natalia Sakurai, Akira Cox, Daniel N. Cymbalyuk, Gennady Front Cell Neurosci Neuroscience Coding noxious cold signals, such as the magnitude and rate of temperature change, play essential roles in the survival of organisms. We combined electrophysiological and computational neuroscience methods to investigate the neural dynamics of Drosophila larva cold-sensing Class III (CIII) neurons. In response to a fast temperature change (–2 to –6°C/s) from room temperature to noxious cold, the CIII neurons exhibited a pronounced peak of a spiking rate with subsequent relaxation to a steady-state spiking. The magnitude of the peak was higher for a higher rate of temperature decrease, while slow temperature decrease (–0.1°C/s) evoked no distinct peak of the spiking rate. The rate of the steady-state spiking depended on the magnitude of the final temperature and was higher at lower temperatures. For each neuron, we characterized this dependence by estimating the temperature of the half activation of the spiking rate by curve fitting neuron’s spiking rate responses to a Boltzmann function. We found that neurons had a temperature of the half activation distributed over a wide temperature range. We also found that CIII neurons responded to decrease rather than increase in temperature. There was a significant difference in spiking activity between fast and slow returns from noxious cold to room temperature: The CIII neurons usually stopped activity abruptly in the case of the fast return and continued spiking for some time in the case of the slow return. We developed a biophysical model of CIII neurons using a generalized description of transient receptor potential (TRP) current kinetics with temperature-dependent activation and Ca(2+)-dependent inactivation. This model recapitulated the key features of the spiking rate responses found in experiments and suggested mechanisms explaining the transient and steady-state activity of the CIII neurons at different cold temperatures and rates of their decrease and increase. We conclude that CIII neurons encode at least three types of cold sensory information: the rate of temperature decrease by a peak of the firing rate, the magnitude of cold temperature by the rate of steady spiking activity, and direction of temperature change by spiking activity augmentation or suppression corresponding to temperature decrease and increase, respectively. Frontiers Media S.A. 2022-07-25 /pmc/articles/PMC9358291/ /pubmed/35959471 http://dx.doi.org/10.3389/fncel.2022.831803 Text en Copyright © 2022 Maksymchuk, Sakurai, Cox and Cymbalyuk. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Maksymchuk, Natalia
Sakurai, Akira
Cox, Daniel N.
Cymbalyuk, Gennady
Transient and Steady-State Properties of Drosophila Sensory Neurons Coding Noxious Cold Temperature
title Transient and Steady-State Properties of Drosophila Sensory Neurons Coding Noxious Cold Temperature
title_full Transient and Steady-State Properties of Drosophila Sensory Neurons Coding Noxious Cold Temperature
title_fullStr Transient and Steady-State Properties of Drosophila Sensory Neurons Coding Noxious Cold Temperature
title_full_unstemmed Transient and Steady-State Properties of Drosophila Sensory Neurons Coding Noxious Cold Temperature
title_short Transient and Steady-State Properties of Drosophila Sensory Neurons Coding Noxious Cold Temperature
title_sort transient and steady-state properties of drosophila sensory neurons coding noxious cold temperature
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358291/
https://www.ncbi.nlm.nih.gov/pubmed/35959471
http://dx.doi.org/10.3389/fncel.2022.831803
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