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犬猫的伊维菌素和哌嗪中毒

Ivermectin and piperazine toxicoses in dogs and cats.

作者信息

Lovell R A

机构信息

Ricerca, Inc., Toxicology and Animal Metabolism, Painesville, Ohio.

出版信息

Vet Clin North Am Small Anim Pract. 1990 Mar;20(2):453-68. doi: 10.1016/s0195-5616(90)50038-8.

Abstract

Review of all reports involving anthelmintics in dogs and cats to the IAPIC between January 1, 1986 and August 10, 1988, revealed that ivermectin (extra-label use) and piperazine accounted for over 50% of the calls assessed as toxicoses and suspected toxicoses. Both ivermectin and piperazine are gamma-aminobutyric acid (GABA) agonists and their major effects appear to be on the central nervous system. Ivermectin toxicoses at estimated doses of greater than or equal to 100-less than 500 micrograms/kg were reported more than once only in the collies (n = 25) and Australian shepherds (n = 10); these two breeds accounted for 46% (69 of 150) of the toxicoses and suspected toxicoses calls in dogs. Ataxia, behavioral disturbances, tremors, mydriasis, weakness/recumbency, apparent blindness, hypersalivation/drooling (dogs only), and coma were the most commonly reported clinical signs in dogs and cats with suspected ivermectin toxicoses. Shock, dyspnea, vomiting, and ataxia were the most common clinical signs attributed to the microfilaricidal activity of ivermectin. Piperazine was the anthelmintic with the greatest number of reports of toxicoses and suspected toxicoses in cats. Piperazine neurotoxicity in cats and dogs usually was manifested by muscle tremors, ataxia, and/or behavioral disturbances within 24 hours after estimated daily dose(s) between 20 and 110 mg/kg.

摘要

对1986年1月1日至1988年8月10日期间向国际动物寄生虫控制协会(IAPIC)报告的所有涉及犬猫驱虫药的病例进行回顾发现,伊维菌素(超适应症使用)和哌嗪占被评估为中毒和疑似中毒病例的50%以上。伊维菌素和哌嗪都是γ-氨基丁酸(GABA)激动剂,它们的主要作用似乎是对中枢神经系统。仅在柯利犬(n = 25)和澳大利亚牧羊犬(n = 10)中不止一次报告了估计剂量大于或等于100微克/千克至小于500微克/千克的伊维菌素中毒病例;这两个品种占犬类中毒和疑似中毒病例的46%(150例中的69例)。共济失调、行为紊乱、震颤、瞳孔散大、虚弱/卧地不起、明显失明、流涎过多(仅犬类)和昏迷是疑似伊维菌素中毒的犬猫中最常报告的临床症状。休克、呼吸困难、呕吐和共济失调是归因于伊维菌素杀微丝蚴活性的最常见临床症状。哌嗪是猫中中毒和疑似中毒报告数量最多的驱虫药。猫和犬的哌嗪神经毒性通常在估计每日剂量为20至110毫克/千克后的24小时内表现为肌肉震颤、共济失调和/或行为紊乱。

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