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The neurotoxic effects of hydrogen peroxide and copper in Retzius nerve cells of the leech Haemopis sanguisuga

Oxidative stress and the generation of reactive oxygen species (ROS) play an important role in cellular damage. Electrophysiological analyses have shown that membrane transport proteins are susceptible to ROS. In the present study, oxidative stress was induced in Retzius nerve cells of the leech Hae...

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Autores principales: Jovanovic, Zorica D., Stanojevic, Marija B., Nedeljkov, Vladimir B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890660/
https://www.ncbi.nlm.nih.gov/pubmed/26935393
http://dx.doi.org/10.1242/bio.014936
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author Jovanovic, Zorica D.
Stanojevic, Marija B.
Nedeljkov, Vladimir B.
author_facet Jovanovic, Zorica D.
Stanojevic, Marija B.
Nedeljkov, Vladimir B.
author_sort Jovanovic, Zorica D.
collection PubMed
description Oxidative stress and the generation of reactive oxygen species (ROS) play an important role in cellular damage. Electrophysiological analyses have shown that membrane transport proteins are susceptible to ROS. In the present study, oxidative stress was induced in Retzius nerve cells of the leech Haemopis sanguisuga by bath application of 1 mM of hydrogen peroxide (H(2)O(2)) and 0.02 mM of copper (Cu) for 20 min. The H(2)O(2)/Cu(II) produced considerable changes in the electrical properties of the Retzius nerve cells. Intracellular recording of the resting membrane potential revealed that the neuronal membrane was depolarized in the presence of H(2)O(2)/Cu(II). We found that the amplitude of action potentials decreased, while the duration augmented in a progressive way along the drug exposure time. The combined application of H(2)O(2) and Cu(II) caused an initial excitation followed by depression of the spontaneous electrical activity. Voltage-clamp recordings revealed a second effect of the oxidant, a powerful inhibition of the outward potassium channels responsible for the repolarization of action potentials. The neurotoxic effect of H(2)O(2)/Cu(II) on the spontaneous spike electrogenesis and outward K(+) current of Retzius nerve cells was reduced in the presence of hydroxyl radical scavengers, dimethylthiourea and dimethyl sulfoxide, but not mannitol. This study provides evidence for the oxidative modification of outward potassium channels in Retzius nerve cells. The oxidative mechanism of the H(2)O(2)/Cu(II) system action on the electrical properties of Retzius neurons proposed in this study might have a wider significance, referring not only to leeches but also to mammalian neurons.
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spelling pubmed-48906602016-06-03 The neurotoxic effects of hydrogen peroxide and copper in Retzius nerve cells of the leech Haemopis sanguisuga Jovanovic, Zorica D. Stanojevic, Marija B. Nedeljkov, Vladimir B. Biol Open Research Article Oxidative stress and the generation of reactive oxygen species (ROS) play an important role in cellular damage. Electrophysiological analyses have shown that membrane transport proteins are susceptible to ROS. In the present study, oxidative stress was induced in Retzius nerve cells of the leech Haemopis sanguisuga by bath application of 1 mM of hydrogen peroxide (H(2)O(2)) and 0.02 mM of copper (Cu) for 20 min. The H(2)O(2)/Cu(II) produced considerable changes in the electrical properties of the Retzius nerve cells. Intracellular recording of the resting membrane potential revealed that the neuronal membrane was depolarized in the presence of H(2)O(2)/Cu(II). We found that the amplitude of action potentials decreased, while the duration augmented in a progressive way along the drug exposure time. The combined application of H(2)O(2) and Cu(II) caused an initial excitation followed by depression of the spontaneous electrical activity. Voltage-clamp recordings revealed a second effect of the oxidant, a powerful inhibition of the outward potassium channels responsible for the repolarization of action potentials. The neurotoxic effect of H(2)O(2)/Cu(II) on the spontaneous spike electrogenesis and outward K(+) current of Retzius nerve cells was reduced in the presence of hydroxyl radical scavengers, dimethylthiourea and dimethyl sulfoxide, but not mannitol. This study provides evidence for the oxidative modification of outward potassium channels in Retzius nerve cells. The oxidative mechanism of the H(2)O(2)/Cu(II) system action on the electrical properties of Retzius neurons proposed in this study might have a wider significance, referring not only to leeches but also to mammalian neurons. The Company of Biologists Ltd 2016-03-02 /pmc/articles/PMC4890660/ /pubmed/26935393 http://dx.doi.org/10.1242/bio.014936 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Jovanovic, Zorica D.
Stanojevic, Marija B.
Nedeljkov, Vladimir B.
The neurotoxic effects of hydrogen peroxide and copper in Retzius nerve cells of the leech Haemopis sanguisuga
title The neurotoxic effects of hydrogen peroxide and copper in Retzius nerve cells of the leech Haemopis sanguisuga
title_full The neurotoxic effects of hydrogen peroxide and copper in Retzius nerve cells of the leech Haemopis sanguisuga
title_fullStr The neurotoxic effects of hydrogen peroxide and copper in Retzius nerve cells of the leech Haemopis sanguisuga
title_full_unstemmed The neurotoxic effects of hydrogen peroxide and copper in Retzius nerve cells of the leech Haemopis sanguisuga
title_short The neurotoxic effects of hydrogen peroxide and copper in Retzius nerve cells of the leech Haemopis sanguisuga
title_sort neurotoxic effects of hydrogen peroxide and copper in retzius nerve cells of the leech haemopis sanguisuga
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890660/
https://www.ncbi.nlm.nih.gov/pubmed/26935393
http://dx.doi.org/10.1242/bio.014936
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