Naidoo Vinny, Mompati Kefiloe Feliciity, Duncan Neil, Taggart Mark Anthony
University of Pretoria Biomedical Research Centre, Faculty of Veterinary Science, University of Pretoria, Private Bag X04, 0110, South Africa.
J Wildl Dis. 2011 Oct;47(4):936-44. doi: 10.7589/0090-3558-47.4.936.
Diclofenac, a nonsteroidal anti-inflammatory drug (NSAID), kills vultures (Gyps spp.) that consume tainted carcasses. As a result, vulture populations in India, Nepal, and Pakistan have been devastated. Studies on meloxicam and ketoprofen demonstrated that the toxicity of the NSAIDs is unpredictable, thereby necessitating individual testing of all available NSAIDs. Because it is no longer practical to use vultures for toxicity testing, we evaluated the Pied Crow (Corvus albus) as a model. Pied Crows (n=6) were exposed to a dose of 0.8 and 10 mg/kg of diclofenac, with no signs of toxicity, and a rapid half-life of elimination. Using primary renal cell and hepatocyte cultures, a high tolerance was demonstrated at the cellular level. Meta-analysis of pharmacokinetic data for the Domestic Chicken (Gallus gallus) and the African White-backed (Gyps africanus), Cape Griffon (Gyps coprotheres), and Turkey Vultures (Cathartes aura) showed a trend toward toxicity when the half-life of elimination increased. We conclude that the crow is not susceptible to diclofenac and, more important, that toxicity in the Gyps species is probably related to zero-order metabolism.
双氯芬酸是一种非甾体抗炎药(NSAID),会杀死食用受污染尸体的秃鹫(兀鹫属)。因此,印度、尼泊尔和巴基斯坦的秃鹫种群遭到了灭顶之灾。对美洛昔康和酮洛芬的研究表明,非甾体抗炎药的毒性不可预测,因此有必要对所有可用的非甾体抗炎药进行个体测试。由于用秃鹫进行毒性测试已不再可行,我们评估了白颈鸦(Corvus albus)作为模型。白颈鸦(n = 6)暴露于0.8和10毫克/千克剂量的双氯芬酸中,未出现毒性迹象,且消除半衰期较短。使用原代肾细胞和肝细胞培养物,在细胞水平上显示出高耐受性。对家鸡(Gallus gallus)以及非洲白背兀鹫(Gyps africanus)、南非兀鹫(Gyps coprotheres)和红头美洲鹫(Cathartes aura)的药代动力学数据进行荟萃分析表明,当消除半衰期增加时,有出现毒性的趋势。我们得出结论,乌鸦对白氯芬酸不敏感,更重要的是,兀鹫属物种的毒性可能与零级代谢有关。