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口服阿莫沙伦与米尔贝肟复方或单方制剂在 MDR1 基因纯合缺失牧羊犬中的安全性。

Safety of oral afoxolaner formulated with or without milbemycin oxime in homozygous MDR1-deficient collie dogs.

机构信息

Boehringer Ingelheim Animal Health, Missouri Research Center, Fulton, Missouri, USA.

Boehringer Ingelheim Animal Health, Lyon, France.

出版信息

J Vet Pharmacol Ther. 2022 Jul;45(4):373-379. doi: 10.1111/jvp.13064. Epub 2022 May 10.

Abstract

Afoxolaner, an insecticide and acaricide compound of the isoxazoline class, is available for dogs as an oral ectoparasiticide medicine (NexGard®) and as an oral endectoparasiticide medicine in combination with milbemycin oxime (MO), a macrocyclic lactone (NexGard® Spectra). The safety of these two compounds, alone or in combination, was investigated in homozygous MDR1-deficient collie dogs, in two studies. Overall, 30 adult collie dogs were treated once orally, 9 with a placebo, 9 with afoxolaner, 6 with MO, and 6 with a combination of afoxolaner and MO. For afoxolaner, the mean investigated dosage corresponded to 3.8 and 4.7 multiples of the maximum recommended therapeutic doses (RTD) in NexGard® and NexGard® Spectra, respectively. For MO, the mean investigated dosage corresponded to 4.7 multiples of the maximum RTD in NexGard® Spectra. Dogs were closely monitored for adverse reactions on the day of treatment and for the following two days. No significant adverse reaction was observed in any dog from the afoxolaner or the afoxolaner + MO groups; in the MO-only treated group, mild and transient neurological signs were observed during the 4-8 h post-treatment window. These studies demonstrated a high level of safety of oral afoxolaner, alone or in combination with milbemycin oxime, in homozygous MDR1-deficient dogs.

摘要

阿福拉纳,一种属于异噁唑啉类的杀虫剂和杀螨剂化合物,可作为口服驱虫药(NexGard®)用于犬类,也可作为口服内寄生虫驱避剂与米尔贝肟(MO)联合使用,后者是一种大环内酯类化合物(NexGard® Spectra)。这两种化合物(单独或联合使用)的安全性已在两种研究中在纯合 MDR1 缺陷型牧羊犬中进行了评估。总体而言,30 只成年牧羊犬接受了一次口服治疗,其中 9 只为安慰剂组,9 只为阿福拉纳组,6 只为 MO 组,6 只为阿福拉纳和 MO 联合组。对于阿福拉纳,所研究的平均剂量分别相当于 NexGard®和 NexGard® Spectra 中最大推荐治疗剂量(RTD)的 3.8 和 4.7 倍。对于 MO,所研究的平均剂量相当于 NexGard® Spectra 中最大 RTD 的 4.7 倍。治疗当天以及接下来的两天,密切监测犬类是否出现不良反应。在阿福拉纳或阿福拉纳+MO 组的任何犬中均未观察到明显的不良反应;在仅接受 MO 治疗的组中,在治疗后 4-8 小时观察到轻度和短暂的神经症状。这些研究表明,口服阿福拉纳单独使用或与米尔贝肟联合使用在纯合 MDR1 缺陷型犬中具有很高的安全性。

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