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The protective effect of hydromorphone to ischemia in rat glial cells

BACKGROUND: Ischemic insults during operation can cause ischemic-reperfusion injuries in brain as well as memory impairments. Total intravenous anesthesia (TIVA) is the preferred anesthetic method in brain surgery, as it utilizes motor evoked potential monitoring. And the use of opioids is common in...

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Autores principales: Kim, Young Sung, Kim, Woon Young, Kim, Yeon-hwa, Yoo, Ji Won, Min, Too Jae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864736/
https://www.ncbi.nlm.nih.gov/pubmed/27247906
http://dx.doi.org/10.1186/s40064-016-2281-7
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author Kim, Young Sung
Kim, Woon Young
Kim, Yeon-hwa
Yoo, Ji Won
Min, Too Jae
author_facet Kim, Young Sung
Kim, Woon Young
Kim, Yeon-hwa
Yoo, Ji Won
Min, Too Jae
author_sort Kim, Young Sung
collection PubMed
description BACKGROUND: Ischemic insults during operation can cause ischemic-reperfusion injuries in brain as well as memory impairments. Total intravenous anesthesia (TIVA) is the preferred anesthetic method in brain surgery, as it utilizes motor evoked potential monitoring. And the use of opioids is common in TIVA. However there are few studies about ischemic protective effect of opioids to glial cells. METHODS: We used mixed cultures of rat glial cells, which were harvested from the brain of 1-day old rat. We divided the experimental groups according to their hydromorphone conditioning period: (a) pre-culture, (b) per-culture, or (c) pre- and per-culture. We measured the levels of the reactive oxygen species (ROS) induced by tert-butyl hydroperoxide (TBH) using flow cytometry. The ROS levels in the glial cells were also measured after the administration of 100 nM hydromorphone and selective opioid receptor antagonists. RESULTS: The ROS levels were reduced in the hydromorphone-treated group, as compared to the control group (only TBH treated). There were no differences between pre-conditioned and per-conditioned groups. However, the ROS levels were more reduced in pre- and per-conditioned group compared to pre-conditioned or per-conditioned only groups. Furthermore, selective antagonists for the delta, kappa, or mu opioid receptor partially negated the hydromorphone effect. CONCLUSION: This study demonstrated that hydromorphone can have additional protective effects on oxidative stress when pre- and per-conditioning is combined. Furthermore we proved that μ, δ, κ opioid receptors participate in protective mechanism of hydromorphone to glial cells.
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spelling pubmed-48647362016-05-31 The protective effect of hydromorphone to ischemia in rat glial cells Kim, Young Sung Kim, Woon Young Kim, Yeon-hwa Yoo, Ji Won Min, Too Jae Springerplus Research BACKGROUND: Ischemic insults during operation can cause ischemic-reperfusion injuries in brain as well as memory impairments. Total intravenous anesthesia (TIVA) is the preferred anesthetic method in brain surgery, as it utilizes motor evoked potential monitoring. And the use of opioids is common in TIVA. However there are few studies about ischemic protective effect of opioids to glial cells. METHODS: We used mixed cultures of rat glial cells, which were harvested from the brain of 1-day old rat. We divided the experimental groups according to their hydromorphone conditioning period: (a) pre-culture, (b) per-culture, or (c) pre- and per-culture. We measured the levels of the reactive oxygen species (ROS) induced by tert-butyl hydroperoxide (TBH) using flow cytometry. The ROS levels in the glial cells were also measured after the administration of 100 nM hydromorphone and selective opioid receptor antagonists. RESULTS: The ROS levels were reduced in the hydromorphone-treated group, as compared to the control group (only TBH treated). There were no differences between pre-conditioned and per-conditioned groups. However, the ROS levels were more reduced in pre- and per-conditioned group compared to pre-conditioned or per-conditioned only groups. Furthermore, selective antagonists for the delta, kappa, or mu opioid receptor partially negated the hydromorphone effect. CONCLUSION: This study demonstrated that hydromorphone can have additional protective effects on oxidative stress when pre- and per-conditioning is combined. Furthermore we proved that μ, δ, κ opioid receptors participate in protective mechanism of hydromorphone to glial cells. Springer International Publishing 2016-05-12 /pmc/articles/PMC4864736/ /pubmed/27247906 http://dx.doi.org/10.1186/s40064-016-2281-7 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Kim, Young Sung
Kim, Woon Young
Kim, Yeon-hwa
Yoo, Ji Won
Min, Too Jae
The protective effect of hydromorphone to ischemia in rat glial cells
title The protective effect of hydromorphone to ischemia in rat glial cells
title_full The protective effect of hydromorphone to ischemia in rat glial cells
title_fullStr The protective effect of hydromorphone to ischemia in rat glial cells
title_full_unstemmed The protective effect of hydromorphone to ischemia in rat glial cells
title_short The protective effect of hydromorphone to ischemia in rat glial cells
title_sort protective effect of hydromorphone to ischemia in rat glial cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864736/
https://www.ncbi.nlm.nih.gov/pubmed/27247906
http://dx.doi.org/10.1186/s40064-016-2281-7
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