Safety of Credelio Quattro™ (lotilaner, moxidectin, praziquantel, and pyrantel chewable tablets) in homozygous MDR1-mutant collie dogs.

IF 3 2区 医学 Q1 PARASITOLOGY
Kari L Riggs, Xinshuo Wang, Scott Wiseman
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引用次数: 0

Abstract

Background: Multidrug resistance-1 (MDR1) mutant dogs have diminished or lack P-glycoprotein (Pgp) expression at the blood-brain barrier and are therefore more susceptible to neurotoxicity caused by macrocyclic lactones and other Pgp substrates due to increased drug penetration into the brain. Therefore, the safety of products containing macrocyclic lactones are required to be evaluated in this sensitive population. Credelio Quattro (lotilaner, moxidectin, praziquantel, and pyrantel chewable tablets) is a novel endectocide for monthly oral administration in dogs. As moxidectin is a macrocyclic lactone, Credelio Quattro was administered to homozygous MDR1 mutant Collie dogs to evaluate the safety of the product.

Methods: The study employed a completely randomized and blinded design, where dogs were allocated to one of four treatment groups. A total of 32 dogs were divided into 4 groups (placebo control, 1×, 2×, or 5×, the maximum recommended labeled dose of Credelio Quattro) each consisting of 8 dogs. Treatment was administered on 3 consecutive occasions, 28 days apart. Dogs were evaluated pre-dose and through 72-h post-treatment using the avermectin sensitive (AVS) categories of seizures or convulsions, ataxia, depression, mydriasis, muscle tremors, and salivation/drooling/vomiting. The assessment of safety was based on AVS scores, general health observations, body weight, and physical examinations.

Results: Credelio Quattro was well tolerated with no serious adverse events. There were no incidents of seizures or convulsions, ataxia, mydriasis, or muscle tremors observed. Salivation/drooling/vomiting was the most frequent observation, occurring in all groups, and most frequently in the 5× group. Vomiting is a dose-dependent effect observed for Credelio Quattro in healthy dogs and is therefore unlikely to represent a neurological effect in MDR1 dogs. Depression was observed in one dog in each of the 0×, 2×, and 5× groups. This was likely a spurious result versus true toxicity, as the sign was subtle and occurred singularly including at 0×. For all AVS signs, the events were transient, and dogs recovered without any intervention.

Conclusions: Credelio Quattro was well tolerated and is safe in MDR1 mutant dogs up to 5× the maximum recommended dose following three consecutive monthly administrations.

Credelio Quattro™(洛替拉尼、莫西菌素、吡喹酮和吡喃酮咀嚼片)在mdr1纯合子突变牧羊犬中的安全性
背景:多药耐药-1 (MDR1)突变犬在血脑屏障处p -糖蛋白(Pgp)表达减少或缺乏,因此由于药物渗入大脑的增加,更容易受到大环内酯和其他Pgp底物引起的神经毒性的影响。因此,含有大环内酯的产品的安全性需要在这一敏感人群中进行评估。Credelio Quattro(洛替拉尼、莫西丁、吡喹酮和吡喃酮咀嚼片)是一种新型的灭虫药,每月口服给狗。由于莫西丁素是一种大环内酯,我们将Credelio Quattro应用于纯合子MDR1突变型柯利犬,以评估该产品的安全性。方法:研究采用完全随机盲法设计,将狗分为四个治疗组。32只狗被分为4组(安慰剂对照组、1x、2x和5x, Credelio Quattro推荐的最大标签剂量),每组8只狗。治疗连续3次,间隔28 d。在给药前和给药后72小时,用阿维菌素敏感(AVS)分类评估狗的癫痫发作或抽搐、共济失调、抑郁、流泪、肌肉震颤和流涎/流口水/呕吐。安全性评估基于AVS评分、一般健康观察、体重和体格检查。结果:Credelio Quattro耐受性良好,无严重不良反应。没有观察到癫痫发作或惊厥、共济失调、肌肉松弛或肌肉震颤的事件。流涎/流口水/呕吐是最常见的观察结果,在所有组中均出现,以5x组最常见。Credelio Quattro在健康犬中观察到呕吐是一种剂量依赖性效应,因此不太可能代表MDR1犬的神经系统效应。0x、2x和5x组各有1只狗出现抑郁。这可能是一个虚假的结果,而不是真正的毒性,因为该迹象很微妙,并且在0×时发生。对于所有AVS症状,事件都是短暂的,狗在没有任何干预的情况下恢复。结论:Credelio Quattro在MDR1突变犬中耐受性良好,并且在连续三个月给药后达到最大推荐剂量的5倍是安全的。
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来源期刊
Parasites & Vectors
Parasites & Vectors 医学-寄生虫学
CiteScore
6.30
自引率
9.40%
发文量
433
审稿时长
1.4 months
期刊介绍: Parasites & Vectors is an open access, peer-reviewed online journal dealing with the biology of parasites, parasitic diseases, intermediate hosts, vectors and vector-borne pathogens. Manuscripts published in this journal will be available to all worldwide, with no barriers to access, immediately following acceptance. However, authors retain the copyright of their material and may use it, or distribute it, as they wish. Manuscripts on all aspects of the basic and applied biology of parasites, intermediate hosts, vectors and vector-borne pathogens will be considered. In addition to the traditional and well-established areas of science in these fields, we also aim to provide a vehicle for publication of the rapidly developing resources and technology in parasite, intermediate host and vector genomics and their impacts on biological research. We are able to publish large datasets and extensive results, frequently associated with genomic and post-genomic technologies, which are not readily accommodated in traditional journals. Manuscripts addressing broader issues, for example economics, social sciences and global climate change in relation to parasites, vectors and disease control, are also welcomed.
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