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饮食中使用芬苯达唑治疗不会损害C57BL/6J小鼠的熟练前肢运动功能。

Dietary Fenbendazole Treatment Does Not Impair Skilled Forelimb Motor Function in C57BL/6J Mice.

作者信息

Fracassi Michela, Rodrigues da Silva Thiago, Wilding Laura A, Jones Theresa A

机构信息

1Department of Psychology, Institute for Neuroscience.

2Animal Resources Center, University of Texas at Austin, Austin, Texas.

出版信息

J Am Assoc Lab Anim Sci. 2025 May 1;64(4):1-7. doi: 10.30802/AALAS-JAALAS-24-152.

Abstract

Fenbendazole (FBZ) treatment for pinworm infections is generally safe and effective but not without concern for potential research complications in its application to laboratory animal colonies. Previously, dietary FBZ was found to impair motor performance in C57BL/6N mice, an effect that endured at least 2 wk posttreatment. These findings raised the possibility that FBZ treatment would complicate our own research on poststroke motor function in C57BL/6J mice. Here we present the results of a study that tested this possibility in the context of facility-wide FBZ treatment based on repeated measures in a skilled reaching task that is extremely sensitive to forelimb motor impairments. Mice of both sexes that were proficient in the reaching task were measured in their performance of the task in each of the 4 wk preceding, 7 wk during, and 2 wk after dietary FBZ treatment that alternated weekly between therapeutic and subtherapeutic doses. There was no indication of a notable decrement or other change in reaching performance during or after FBZ treatment (mean ± SE percent success before, during, and after treatment = 57 ± 2, 53 ± 2, and 60 ± 2; n = 20). Performance stability in FBZ-treated mice was similar to that of untreated mice. These results are significant for revealing a lack of noticeable influence of FBZ on a commonly used measure of motor function in a widely used mouse strain. The difference in FBZ effects relative to the prior study could reflect substrain-dependency (6N compared with 6J) and/or differences in motor behavioral measures.

摘要

芬苯达唑(FBZ)治疗蛲虫感染通常是安全有效的,但在应用于实验动物群体时,其潜在的研究并发症也不容忽视。此前研究发现,在C57BL/6N小鼠中,经口摄入FBZ会损害运动能力,且这种影响在治疗后至少持续2周。这些发现增加了一种可能性,即FBZ治疗可能会使我们自己关于C57BL/6J小鼠中风后运动功能的研究变得复杂。在此,我们展示了一项研究结果,该研究在全设施范围内进行FBZ治疗的背景下测试了这种可能性,所采用的方法是在一项对前肢运动损伤极为敏感的熟练抓握任务中进行重复测量。对熟练掌握抓握任务的雌雄小鼠,在饮食中给予FBZ治疗前的4周、治疗期间的7周以及治疗后的2周内,每周交替给予治疗剂量和亚治疗剂量,并测量它们在该任务中的表现。在FBZ治疗期间或之后,没有迹象表明抓握表现有显著下降或其他变化(治疗前、治疗期间和治疗后的平均成功率±标准误分别为57±2、53±2和60±2;n = 20)。接受FBZ治疗的小鼠的表现稳定性与未治疗的小鼠相似。这些结果对于揭示FBZ对一种广泛使用的小鼠品系中常用的运动功能测量指标没有明显影响具有重要意义。相对于先前的研究,FBZ效应的差异可能反映了亚品系依赖性(6N与6J相比)和/或运动行为测量指标的差异。

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