Abstract:The aim of this study was to evaluate short-term intravenous anaesthesia with alfaxalone in green iguanas (Iguana iguana). Alfaxalone at a dose rate of 5 mg/kg was administered to thirteen adult male green iguanas via the ventral caudal vein following 24 h fasting. The induction time, tracheal tube insertion time, surgical plane of anaesthesia interval, and full recovery time were recorded. Systolic, diastolic and mean arterial blood pressure (measured indirectly), pulse rate, respiratory rate, SpO 2 and ETCO … Show more
“…12 A number of reports have since been published describing the use of alfaxalone in reptiles. [120][121][122] Alfaxalone is currently a preferred induction agent, when available, and should be used together with analgesic agents and followed by endotracheal intubation, positive pressure ventilation, and gas anesthesia.…”
Section: Analgesic and Anesthetic Agents ______mentioning
“…12 A number of reports have since been published describing the use of alfaxalone in reptiles. [120][121][122] Alfaxalone is currently a preferred induction agent, when available, and should be used together with analgesic agents and followed by endotracheal intubation, positive pressure ventilation, and gas anesthesia.…”
Section: Analgesic and Anesthetic Agents ______mentioning
“…Whereas cats receiving 5 mg/kg had a recovery time of about 45 minutes, and dogs receiving 6 mg/kg had a recovery time of about 30 minutes, likely resulting from a more rapid metabolism in mammals [19,20]. In other reptiles, such as the ball python and green iguana intramuscular administration of three different doses of Alfaxalone resulted in a maximum effect within 10 minutes [22,23] James et al, 2017. Similarly, Knotek et al (2013) looked at short-term anesthesia with Alfaxalone in green iguanas at a dose rate of 5 mg/ kg, and found both rapid induction, where loss of the toe-pinch reflex occurred at 2.3 minutes, and rapid recovery to full activity in about 14 min after injection.…”
Anoxia in the mammalian brain leads to hyper-excitability and cell death; however, this cascade of events does not occur in the anoxia-tolerant brain of the western painted turtle, Chrysemys picta belli. The painted turtle has become an important anoxia-tolerant model to study brain, heart, and liver function in the absence of oxygen, but being anoxia-tolerant likely means that decapitation alone is not a suitable method of euthanasia. Many anesthetics have long-term effects on ion channels and are not appropriate for same day experimentation. Using whole-cell electrophysiological techniques, we examine the effects of the anesthetic, Alfaxalone, on pyramidal cell action potential amplitude, threshold, rise and decay time, width, frequency, whole cell conductance, and evoked GABAA receptors currents to determine if any of these characteristics are altered with the use of Alfaxalone for animal sedation. We find that Alfaxalone has no long-term impact on action potential parameters or whole-cell conductance. When acutely applied to naïve tissue, Alfaxalone did lengthen GABAA receptor current decay rates by 1.5-fold. Following whole-animal sedation with Alfaxalone, evoked whole cell GABAA receptor current decay rates displayed an increasing trend with 1 and 2 hours after brain sheet preparation, but showed no significant change after a 3-hour washout period. Therefore, we conclude that Alfaxalone is a suitable anesthetic for same day use in electrophysiological studies in western painted turtle brain tissue.
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