“Getting Under the Hood” of Neuronal Signaling in

Caenorhabditis elegans is a powerful model to study the neural and biochemical basis of behavior. It combines a small, completely mapped nervous system, powerful genetic tools, and a transparent cuticle, allowing Ca ++ imaging without the need for dissection. However, these approaches remain one ste...

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Main Authors: Paul DE Williams, Jeffrey A Zahratka, Bruce A Bamber
Format: Article
Language:English
Published: SAGE Publishing 2018-06-01
Series:Journal of Experimental Neuroscience
Online Access:https://doi.org/10.1177/1179069518781326
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spelling doaj-ecdcdd70dbba4eba8da40dd3a90ba9c12020-11-25T02:47:50ZengSAGE PublishingJournal of Experimental Neuroscience1179-06952018-06-011210.1177/1179069518781326“Getting Under the Hood” of Neuronal Signaling in Paul DE Williams0Jeffrey A Zahratka1Bruce A Bamber2Department of Biomedical Sciences, Iowa State University, Ames, IA, USADepartment of Neuroscience, Baldwin Wallace University, Berea, OH, USADepartment of Biological Sciences, The University of Toledo, Toledo, OH, USACaenorhabditis elegans is a powerful model to study the neural and biochemical basis of behavior. It combines a small, completely mapped nervous system, powerful genetic tools, and a transparent cuticle, allowing Ca ++ imaging without the need for dissection. However, these approaches remain one step removed from direct pharmacological and physiological characterization of individual neurons. Much can still be learned by “getting under the hood” or breaching the cuticle and directly studying the neurons. For example, we recently combined electrophysiology, Ca ++ imaging, and pharmacological analysis on partially dissected ASH nociceptors showing that serotonin (5-HT) potentiates depolarization by inhibiting Ca ++ influx. This study challenges the tacit assumption that Ca ++ transient amplitudes and depolarization strength are positively correlated and has validated a new paradigm for interpreting Ca ++ signals. Bypassing the cuticle was critical for the success of these experiments, not only for performing electrical recordings but also for the acute and reversible application of drugs. By contrast, drug soaking or mutating genes can produce long-term effects and compensatory changes, potentially confounding interpretations significantly. Therefore, direct studies of the physiological response of individual neurons should remain a critical objective, to provide key molecular insights complementing global Ca ++ imaging neural network studies.https://doi.org/10.1177/1179069518781326
collection DOAJ
language English
format Article
sources DOAJ
author Paul DE Williams
Jeffrey A Zahratka
Bruce A Bamber
spellingShingle Paul DE Williams
Jeffrey A Zahratka
Bruce A Bamber
“Getting Under the Hood” of Neuronal Signaling in
Journal of Experimental Neuroscience
author_facet Paul DE Williams
Jeffrey A Zahratka
Bruce A Bamber
author_sort Paul DE Williams
title “Getting Under the Hood” of Neuronal Signaling in
title_short “Getting Under the Hood” of Neuronal Signaling in
title_full “Getting Under the Hood” of Neuronal Signaling in
title_fullStr “Getting Under the Hood” of Neuronal Signaling in
title_full_unstemmed “Getting Under the Hood” of Neuronal Signaling in
title_sort “getting under the hood” of neuronal signaling in
publisher SAGE Publishing
series Journal of Experimental Neuroscience
issn 1179-0695
publishDate 2018-06-01
description Caenorhabditis elegans is a powerful model to study the neural and biochemical basis of behavior. It combines a small, completely mapped nervous system, powerful genetic tools, and a transparent cuticle, allowing Ca ++ imaging without the need for dissection. However, these approaches remain one step removed from direct pharmacological and physiological characterization of individual neurons. Much can still be learned by “getting under the hood” or breaching the cuticle and directly studying the neurons. For example, we recently combined electrophysiology, Ca ++ imaging, and pharmacological analysis on partially dissected ASH nociceptors showing that serotonin (5-HT) potentiates depolarization by inhibiting Ca ++ influx. This study challenges the tacit assumption that Ca ++ transient amplitudes and depolarization strength are positively correlated and has validated a new paradigm for interpreting Ca ++ signals. Bypassing the cuticle was critical for the success of these experiments, not only for performing electrical recordings but also for the acute and reversible application of drugs. By contrast, drug soaking or mutating genes can produce long-term effects and compensatory changes, potentially confounding interpretations significantly. Therefore, direct studies of the physiological response of individual neurons should remain a critical objective, to provide key molecular insights complementing global Ca ++ imaging neural network studies.
url https://doi.org/10.1177/1179069518781326
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