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氟哌啶醇和阿扎哌隆在驱赶网捕获的南欧岩羚羊(比利牛斯岩羚羊)中的应用。

Haloperidol and azaperone in drive-net captured Southern chamois (Rupicapra pyrenaica).

作者信息

Mentaberre G, López-Olvera J R, Casas-Díaz E, Marco I, Lavín S

机构信息

Servei d'Ecopatologia de Fauna Salvatge, Facultat de Veterinària, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain.

出版信息

J Wildl Dis. 2010 Jul;46(3):923-8. doi: 10.7589/0090-3558-46.3.923.

Abstract

We investigated the effect of haloperidol and azaperone in drive-net captured Southern chamois (Rupicapra pyrenaica). Both tranquilizers have been successfully used in a wide range of wild species for reducing postcapture stress response. During 2005, 39 free-ranging chamois were captured, randomly injected intramuscularly with haloperidol (0.29 +/- 0.12 mg/kg; n=24), azaperone (1.1 +/- 0.82 mg/kg; n=6), or saline (0.5 ml; n=9), and restrained for 3 hr. Heart rate was higher in the treated chamois; erythrocyte parameters and total protein concentration decreased over time owing to splenic sequestration, hemodilution, vasodilation, and reflex tachycardia. Creatinine, sodium, and chloride remained stable only in the haloperidol-treated group, suggesting an improvement in renal perfusion. Nevertheless, the azaperone-treated chamois displayed higher body temperature, and both treated groups had higher serum muscular enzymes than the control group, suggesting higher muscle stress. These results lead us not to recommend the use of these tranquilizers-especially azaperone-as first-choice neuroleptics in chamois.

摘要

我们研究了氟哌啶醇和阿扎哌隆对驱赶网捕获的南阿尔卑斯岩羚羊(Rupicapra pyrenaica)的影响。这两种镇静剂已成功用于多种野生动物,以减轻捕获后的应激反应。2005年期间,捕获了39只自由放养的岩羚羊,随机肌肉注射氟哌啶醇(0.29±0.12mg/kg;n = 24)、阿扎哌隆(1.1±0.82mg/kg;n = 6)或生理盐水(0.5ml;n = 9),并约束3小时。经治疗的岩羚羊心率较高;由于脾扣押、血液稀释、血管舒张和反射性心动过速,红细胞参数和总蛋白浓度随时间下降。仅在氟哌啶醇治疗组中,肌酐、钠和氯保持稳定,提示肾灌注改善。然而,阿扎哌隆治疗的岩羚羊体温较高,且两个治疗组的血清肌肉酶均高于对照组,提示肌肉应激较高。这些结果使我们不建议在岩羚羊中使用这些镇静剂,尤其是阿扎哌隆作为首选抗精神病药物。

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