Physiological disturbance may contribute to neurodegeneration induced by isoflurane or sevoflurane in 14 day old rats.

BACKGROUND: Volatile anesthetics are widely used in pediatric anesthesia but their potential neurotoxicity raise significant concerns regarding sequelae after anesthesia. However, whether physiological disturbance during anesthetic exposure contributes to such side effects remains unknown. The aim o...

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Main Authors: Binbin Wu, Zipu Yu, Shan You, Yihu Zheng, Jin Liu, Yajing Gao, Han Lin, Qingquan Lian
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3882250?pdf=render
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spelling doaj-52b81ff384ea4209a71af73b514912f72020-11-25T02:08:42ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0191e8462210.1371/journal.pone.0084622Physiological disturbance may contribute to neurodegeneration induced by isoflurane or sevoflurane in 14 day old rats.Binbin WuZipu YuShan YouYihu ZhengJin LiuYajing GaoHan LinQingquan LianBACKGROUND: Volatile anesthetics are widely used in pediatric anesthesia but their potential neurotoxicity raise significant concerns regarding sequelae after anesthesia. However, whether physiological disturbance during anesthetic exposure contributes to such side effects remains unknown. The aim of the current study is to compare the neurotoxic effects of isoflurane and sevoflurane in 14 day old rat pups under spontaneous breathing or ventilated conditions. METHODS: Postnatal 14 day rats were assigned to one of five groups: 1) spontaneous breathing (SB) + room air (control, n = 17); 2) SB + isoflurane (n = 35); 3) SB + sevoflurane (n = 37); 4) mechanical ventilation (MV) + isoflurane (n = 29); 5) MV + sevoflurane (n = 32). Anesthetized animal received either 1.7% isoflurane or 2.4% seveoflurane for 4 hours. Arterial blood gases and blood pressure were monitored in the anesthetized groups. Neurodegeneration in the CA3 region of hippocampus was assessed with terminal deoxynucleotidyl transferase-mediated DNA nick-end labeling immediately after exposure. Spatial learning and memory were evaluated with the Morris water maze in other cohorts 14 days after experiments. RESULTS: Most rats in the SB groups developed physiological disturbance whereas ventilated rats did not but become hyperglycemic. Mortality from anesthesia in the SB groups was significantly higher than that in the MV groups. Cell death in the SB but not MV groups was significantly higher than controls. SB + anesthesia groups performed worse on the Morris water maze behavioral test, but no deficits were found in the MV group compared with the controls. CONCLUSIONS: These findings could suggest that physiological disturbance induced by isoflurane or sevoflurane anesthesia may also contribute to their neurotoxicity.http://europepmc.org/articles/PMC3882250?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Binbin Wu
Zipu Yu
Shan You
Yihu Zheng
Jin Liu
Yajing Gao
Han Lin
Qingquan Lian
spellingShingle Binbin Wu
Zipu Yu
Shan You
Yihu Zheng
Jin Liu
Yajing Gao
Han Lin
Qingquan Lian
Physiological disturbance may contribute to neurodegeneration induced by isoflurane or sevoflurane in 14 day old rats.
PLoS ONE
author_facet Binbin Wu
Zipu Yu
Shan You
Yihu Zheng
Jin Liu
Yajing Gao
Han Lin
Qingquan Lian
author_sort Binbin Wu
title Physiological disturbance may contribute to neurodegeneration induced by isoflurane or sevoflurane in 14 day old rats.
title_short Physiological disturbance may contribute to neurodegeneration induced by isoflurane or sevoflurane in 14 day old rats.
title_full Physiological disturbance may contribute to neurodegeneration induced by isoflurane or sevoflurane in 14 day old rats.
title_fullStr Physiological disturbance may contribute to neurodegeneration induced by isoflurane or sevoflurane in 14 day old rats.
title_full_unstemmed Physiological disturbance may contribute to neurodegeneration induced by isoflurane or sevoflurane in 14 day old rats.
title_sort physiological disturbance may contribute to neurodegeneration induced by isoflurane or sevoflurane in 14 day old rats.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description BACKGROUND: Volatile anesthetics are widely used in pediatric anesthesia but their potential neurotoxicity raise significant concerns regarding sequelae after anesthesia. However, whether physiological disturbance during anesthetic exposure contributes to such side effects remains unknown. The aim of the current study is to compare the neurotoxic effects of isoflurane and sevoflurane in 14 day old rat pups under spontaneous breathing or ventilated conditions. METHODS: Postnatal 14 day rats were assigned to one of five groups: 1) spontaneous breathing (SB) + room air (control, n = 17); 2) SB + isoflurane (n = 35); 3) SB + sevoflurane (n = 37); 4) mechanical ventilation (MV) + isoflurane (n = 29); 5) MV + sevoflurane (n = 32). Anesthetized animal received either 1.7% isoflurane or 2.4% seveoflurane for 4 hours. Arterial blood gases and blood pressure were monitored in the anesthetized groups. Neurodegeneration in the CA3 region of hippocampus was assessed with terminal deoxynucleotidyl transferase-mediated DNA nick-end labeling immediately after exposure. Spatial learning and memory were evaluated with the Morris water maze in other cohorts 14 days after experiments. RESULTS: Most rats in the SB groups developed physiological disturbance whereas ventilated rats did not but become hyperglycemic. Mortality from anesthesia in the SB groups was significantly higher than that in the MV groups. Cell death in the SB but not MV groups was significantly higher than controls. SB + anesthesia groups performed worse on the Morris water maze behavioral test, but no deficits were found in the MV group compared with the controls. CONCLUSIONS: These findings could suggest that physiological disturbance induced by isoflurane or sevoflurane anesthesia may also contribute to their neurotoxicity.
url http://europepmc.org/articles/PMC3882250?pdf=render
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