Roug Annette, Nol Pauline, Mama Khursheed
Alaska Department of Fish and Game, Palmer, AK 99645, USA,
Colorado Parks and Wildlife, Fort Collins, CO 80521, USA.
J Zoo Wildl Med. 2024 Mar;55(1):136-142. doi: 10.1638/2023-0049.
A mixture of butorphanol, azaperone, and medetomidine (BAM) is frequently used for immobilization of North American hoofstock. Common adverse effects include respiratory depression, hypoxemia, and bradycardia. In this nonblinded crossover study the efficacy of two a-2 adrenergic antagonists, tolazoline and vatinoxan, were evaluated in alleviating adverse effects of BAM in Rocky Mountain elk (). Early administration of these antagonists was hypothesized to cause an increase in heart rate, respiratory rate, partial pressure of oxygen (PaO) and hemoglobin oxygen saturation (SpO), as well as reduction in mean arterial blood pressure without affecting sedation levels. Eight captive adult female elk were immobilized on three separate occasions at least 14 d apart with 0.15 mg/kg butorphanol, 0.05 mg/kg azaperone, and 0.06 mg/kg medetomidine. Tolazoline (2 mg/kg IM), vatinoxan (3 mg/mg medetomidine IV) or sterile saline (2 ml IM) were administered 20 min postinduction. The BAM caused hypoxemia, bradycardia, and moderate hypertension, and because of the severe hypoxemia observed, all animals received intratracheal oxygen throughout immobilization. Heart rate, respiratory rate, rectal temperature, SpO, PaO, and systolic, diastolic, and mean arterial blood pressure were monitored every 5 min throughout the immobilization. Intramuscular tolazoline caused a brief but significant drop in mean arterial pressure compared with controls and a brief but nonsignificant increase in heart rate. Vatinoxan caused a significant drop in blood pressure and a brief significant increase in heart rate. Changes in respiratory rates and PaO were not observed with either antagonist; however, all animals received oxygen, which may have influenced this result. The depth of sedation was unchanged after administration of either drug.
布托啡诺、氮哌酮和美托咪定的混合物(BAM)常用于北美有蹄类动物的保定。常见的不良反应包括呼吸抑制、低氧血症和心动过缓。在这项非盲交叉研究中,评估了两种α-2肾上腺素能拮抗剂托拉唑啉和瓦替诺生在减轻落基山麋鹿BAM不良反应方面的效果。假设早期给予这些拮抗剂会导致心率、呼吸频率、氧分压(PaO)和血红蛋白氧饱和度(SpO)增加,同时平均动脉血压降低,且不影响镇静水平。八只圈养成年雌性麋鹿在至少间隔14天的三个不同时间点,用0.15mg/kg布托啡诺、0.05mg/kg氮哌酮和0.06mg/kg美托咪定进行保定。诱导后20分钟给予托拉唑啉(2mg/kg肌肉注射)、瓦替诺生(3mg/美托咪定mg静脉注射)或无菌生理盐水(2ml肌肉注射)。BAM导致低氧血症、心动过缓和中度高血压,由于观察到严重的低氧血症,所有动物在保定期间都接受了气管内输氧。在整个保定过程中,每5分钟监测一次心率、呼吸频率、直肠温度、SpO、PaO以及收缩压、舒张压和平均动脉血压。与对照组相比,肌肉注射托拉唑啉导致平均动脉压短暂但显著下降,心率短暂但不显著增加。瓦替诺生导致血压显著下降,心率短暂显著增加。两种拮抗剂均未观察到呼吸频率和PaO的变化;然而,所有动物都接受了氧气,这可能影响了该结果。给予任何一种药物后,镇静深度均未改变。