Research paperEffects of a single intravenous bolus of fentanyl on the minimum anesthetic concentration of isoflurane in chickens (Gallus gallus domesticus)
Introduction
Isoflurane is the most commonly used inhalation anesthetic agent in birds owing to its low blood–gas partition coefficient, which allows both rapid induction of, and recovery from, anesthesia and also because its elimination is not dependent on metabolic or excretory pathways (Ludders 2015). Concomitant administration of injectable and inhalation anesthetics may reduce the dose of inhalation agent required, resulting in not only less cardiopulmonary depression but also possible blunting of the sympathetic response to stimulation during surgery (Gunkel & Lafortune 2005).
Morphine decreased the minimum anesthetic concentration (MAC) of isoflurane by 52% in chickens (Concannon et al. 1995), and butorphanol reduced the isoflurane MAC in cockatoos by 25% (Curro et al. 1994). However, neither study evaluated the temporal effect of the opioid administration on isoflurane MAC. The duration of the anesthetic-sparing effect of opioids during inhalation anesthesia in birds is reported to be short. In the guineafowl, intravenous (IV) administration of butorphanol (4 mg kg−1) reduced the sevoflurane MAC at 15 and 30 minutes by 21% and 11%, respectively (Escobar et al. 2012); however, this dosage was considered unsafe (Escobar et al. 2014). Intramuscular (IM) administration of morphine (3 or 6 mg kg−1) in chickens reduced the isoflurane MAC at 15 minutes by 15% and 22%, respectively (Vela et al. 2014). Methadone (6 mg kg−1) IM decreased isoflurane MAC by 30% at 15 minutes after administration in chickens; however, the effect was gone by 30 minutes (Escobar et al. 2016).
Fentanyl is a μ-opioid agonist with a short onset and duration of effect when administered as a single IV bolus (Kukanich & Wiese 2015). The results of a study of target-controlled infusions of fentanyl on isoflurane MAC in red-tailed hawks identified a plasma concentration-dependent reduction in MAC of up to 55% (Pavez et al. 2011). That study maintained constant plasma fentanyl concentrations; thus, the temporal effects of a bolus of fentanyl on isoflurane MAC were not examined.
The purpose of this study was to evaluate the temporal effects of an IV fentanyl bolus on isoflurane MAC in chickens and to measure selected cardiopulmonary variables. We hypothesized that a single bolus of fentanyl would induce a dose-dependent reduction in isoflurane MAC for a minimum of 15 minutes in chickens. We also hypothesized that the combination of fentanyl and isoflurane would not result in a greater cardiopulmonary depression when compared with an equipotent isoflurane concentration.
Section snippets
Material and methods
This study was approved by the Institutional Animal Care and Use Committee of the School of Agricultural and Veterinarian Sciences, São Paulo State University (no. 008078/13).
First phase
Individual isoflurane MAC was determined in three of the four birds in which it had not previously been determined. Mean ± SD isoflurane MAC for the three birds was 1.1 ± 0.1%. The fourth bird simultaneously extubated itself and regurgitated and aspirated gastric content during MAC determination, resulting in death. No adverse effects were noted during and after fentanyl administration. At 5 and 15 minutes after fentanyl (10 μg kg−1) administration, isoflurane MAC was reduced by 17.6% (6.1–29.1%)
Discussion
The present study reports that the administration of a fentanyl bolus dose-dependently reduces the isoflurane MAC in chickens for <15 minutes. The higher dose tested reduced isoflurane MAC by 43%, which was similar to another study involving red-tailed hawks, in which isoflurane MAC reduction ranged from 31% to 55% after fentanyl target-controlled infusions (Pavez et al. 2011). However, neither dose of fentanyl studied caused significant reduction in isoflurane MAC at 15 minutes after
Acknowledgements
The authors thank the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for funding this study (no. 475127/2012-9) and thank Nathan da Rocha Neves Cruz and Camila Angelica Gonçalves for helping with the study development.
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