对化学固定的生理反应:以肯尼亚自由放养的平原斑马(Equus quagga)为例

F. Vitali, E. Kariuki, M. Njoroge, T. Kaitho, G. Curone, D. Mijele, G. Ravasio
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引用次数: 1

摘要

野生斑马的可预测固定是具有挑战性的,不同物种的鸦片反应存在巨大差异。依托啡联合阿扎哌酮被认为是首选方案,但没有研究调查了平原斑马对这种固定程序的生理反应。在肯尼亚,对11头自由放养的平原斑马(Equus quagga)施以0.019±0.003 mg/kg的艾托啡和0.27±0.05 mg/kg的阿扎哌酮,并用射镖联合肌肉注射。平卧后,每5分钟取动脉标本进行血气分析和生理参数记录。对高速追逐造成的用力以及诱导、固定和恢复的质量进行描述性评分。二丙诺啡或纳曲酮用于阿片类药物拮抗剂。在所有斑马中,该组合在3.5±0.8分钟内诱导快速诱导,并在整个固定期间提供可靠的卧位,而无需尝试站立。平均心率为102±42次/分钟,呼吸频率为18±4次/分钟,平均动脉血压为145±28 mmHg。动脉气体分析显示轻度至重度和部分代偿性代谢性酸中毒和缺氧,而电解质在正常范围内。特别是,追逐过程中较高的运动水平与较差的固定评分(p=0.008)和高热(p=0.0012)显著相关,而与更严重的酸中毒不显著相关。二丙诺啡/纳曲酮给药后平均恢复时间为121±38秒,麻醉恢复顺利。艾托啡-阿扎哌酮联合用药可引起放养平原斑马心动过速、高血压、代谢性酸中毒和低氧血症等生理变化。然而,这些初步结果表明,高速追逐可能是导致生理失衡的原因,而这种药物组合并不会抑制代偿反应。无论代谢状态如何,从固定状态中恢复是平稳的,此后所有斑马都恢复了正常的行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Physiological response to chemical immobilization: a case study of etorphine-azaperone in free-ranging plains zebra (Equus quagga) in Kenya
Predictable immobilization of wild zebras is challenging and there is massive variation in opiate response within different species. Etorphine combined with azaperone is considered the protocol of choice, but no studies have investigated the physiological response to this procedure of immobilization in plains zebras. Eleven free-ranging plains zebras ( Equus quagga ) were immobilized in Kenya using a combination of etorphine 0.019 ± 0.003 mg/kg and azaperone 0.27 ± 0.05 mg/kg administered intramuscularly with a projectile dart. After recumbency, an arterial sample was performed for blood gas analysis and physiological parameters were recorded every five minutes. Descriptive scores were given to the exertion resulting from high-speed chasing and to the quality of induction, immobilization and recovery. Diprenorphine or naltrexone were used for opioid antagonism. In all zebras, the combination induced quick inductions within 3.5 ± 0.8 minutes and provided reliable recumbencies without attempts to stand for the entire duration of the immobilization. The average heart rates, respiratory rates and mean arterial blood pressure recorded were 102 ± 42 beats/minute, 18 ± 4 breaths/minute and 145 ± 28 mmHg respectively. Arterial gas analyses demonstrated mild to severe and partially compensated metabolic acidosis and hypoxia, while electrolytes were within equids range. In particular, higher exertion levels during the chasing were significantly correlated to worse immobilization scores (p=0.008) and hyperthermia occurrence (p=0.0012) and non-significantly to more severe acidosis. Recoveries from anaesthesia were smooth, on average 121 ± 38 seconds after diprenorphine/naltrexone administration. Etorphine-azaperone combination produced physiological alterations in free-ranging plains zebra such as tachycardia, hypertension, metabolic acidosis and hypoxemia. However, these preliminary results indicate that high-speed chase might be responsible for the physiological imbalance and that this drug combination does not suppress the compensatory response. Regardless of the metabolic status, recover from immobilization was uneventful and all zebras went back to normal behavior thereafter.
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