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Pharmacological properties of various anesthetic protocols in 10-day-old neonatal rats

In general, the anesthesia in neonates involves high risk. Although hypothermic anesthesia is recommended in rats up to the age of 7 days, neonatal anesthesia for later periods has not been standardized. The present study investigated the pharmacological properties of conventional anesthetic protoco...

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Autores principales: Tsukamoto, Atsushi, Konishi, Yui, Kawakami, Takako, Koibuchi, Chiharu, Sato, Reiichiro, Kanai, Eiichi, Inomata, Tomo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Association for Laboratory Animal Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682352/
https://www.ncbi.nlm.nih.gov/pubmed/28674271
http://dx.doi.org/10.1538/expanim.17-0037
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author Tsukamoto, Atsushi
Konishi, Yui
Kawakami, Takako
Koibuchi, Chiharu
Sato, Reiichiro
Kanai, Eiichi
Inomata, Tomo
author_facet Tsukamoto, Atsushi
Konishi, Yui
Kawakami, Takako
Koibuchi, Chiharu
Sato, Reiichiro
Kanai, Eiichi
Inomata, Tomo
author_sort Tsukamoto, Atsushi
collection PubMed
description In general, the anesthesia in neonates involves high risk. Although hypothermic anesthesia is recommended in rats up to the age of 7 days, neonatal anesthesia for later periods has not been standardized. The present study investigated the pharmacological properties of conventional anesthetic protocols in 10-day-old SD rats. The rats were anesthetized with four anesthetics: a combination of ketamine and xylazine (K/X); a combination of medetomidine, midazolam, and butorphanol (M/M/B); isoflurane; and sevoflurane. Anesthetic depth was scored by reflex response to noxious stimuli. Induction and recovery times were recorded. Vital signs and mortality rate were evaluated for safety assessment. All rats died after administration of K/X at a dose of 60/6 mg/kg, whereas K/X at 40/4 mg/kg resulted in insufficient anesthetic depth, indicating inappropriate for neonatal anesthesia. Although M/M/B at the adult rat dose (0.15/2/2.5 mg/kg) did not provide surgical anesthetic depth, the mouse dose (0.3/4/5 mg/kg) showed sufficient anesthetic depth with relatively stable vital signs. Isoflurane required a long induction period, and caused remarkable respiratory depression and hypothermia, resulted in a 25% mortality rate. In contrast, sevoflurane provided consistent surgical anesthetic depth with rapid induction. Although respiratory rate decrease was markedly observed, all rats survived. Among the anesthetic protocols investigated in the present study, sevoflurane and M/M/B at the mouse dose were recommended for the neonatal anesthesia. Compared with adult rats, the required dose of both anesthetics in neonates was higher, possibly associated with their lower anesthetic sensitivity.
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spelling pubmed-56823522017-11-16 Pharmacological properties of various anesthetic protocols in 10-day-old neonatal rats Tsukamoto, Atsushi Konishi, Yui Kawakami, Takako Koibuchi, Chiharu Sato, Reiichiro Kanai, Eiichi Inomata, Tomo Exp Anim Original In general, the anesthesia in neonates involves high risk. Although hypothermic anesthesia is recommended in rats up to the age of 7 days, neonatal anesthesia for later periods has not been standardized. The present study investigated the pharmacological properties of conventional anesthetic protocols in 10-day-old SD rats. The rats were anesthetized with four anesthetics: a combination of ketamine and xylazine (K/X); a combination of medetomidine, midazolam, and butorphanol (M/M/B); isoflurane; and sevoflurane. Anesthetic depth was scored by reflex response to noxious stimuli. Induction and recovery times were recorded. Vital signs and mortality rate were evaluated for safety assessment. All rats died after administration of K/X at a dose of 60/6 mg/kg, whereas K/X at 40/4 mg/kg resulted in insufficient anesthetic depth, indicating inappropriate for neonatal anesthesia. Although M/M/B at the adult rat dose (0.15/2/2.5 mg/kg) did not provide surgical anesthetic depth, the mouse dose (0.3/4/5 mg/kg) showed sufficient anesthetic depth with relatively stable vital signs. Isoflurane required a long induction period, and caused remarkable respiratory depression and hypothermia, resulted in a 25% mortality rate. In contrast, sevoflurane provided consistent surgical anesthetic depth with rapid induction. Although respiratory rate decrease was markedly observed, all rats survived. Among the anesthetic protocols investigated in the present study, sevoflurane and M/M/B at the mouse dose were recommended for the neonatal anesthesia. Compared with adult rats, the required dose of both anesthetics in neonates was higher, possibly associated with their lower anesthetic sensitivity. Japanese Association for Laboratory Animal Science 2017-06-30 2017 /pmc/articles/PMC5682352/ /pubmed/28674271 http://dx.doi.org/10.1538/expanim.17-0037 Text en ©2017 Japanese Association for Laboratory Animal Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original
Tsukamoto, Atsushi
Konishi, Yui
Kawakami, Takako
Koibuchi, Chiharu
Sato, Reiichiro
Kanai, Eiichi
Inomata, Tomo
Pharmacological properties of various anesthetic protocols in 10-day-old neonatal rats
title Pharmacological properties of various anesthetic protocols in 10-day-old neonatal rats
title_full Pharmacological properties of various anesthetic protocols in 10-day-old neonatal rats
title_fullStr Pharmacological properties of various anesthetic protocols in 10-day-old neonatal rats
title_full_unstemmed Pharmacological properties of various anesthetic protocols in 10-day-old neonatal rats
title_short Pharmacological properties of various anesthetic protocols in 10-day-old neonatal rats
title_sort pharmacological properties of various anesthetic protocols in 10-day-old neonatal rats
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682352/
https://www.ncbi.nlm.nih.gov/pubmed/28674271
http://dx.doi.org/10.1538/expanim.17-0037
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