Galstyan David S, Kolesnikova Tatyana O, Demin Konstantin A, Dubrovskii Yaroslav A, Murashko Ekaterina, Kessenikh Elizaveta, Ilyin Nikita P, Ikrin Aleksey N, Moskalenko Anastasia M, de Abreu Murilo S, Yang Longen, Kalueff Allan V
World Class Research Center for Personalized Medicine, Almazov National Medical Research Centre, Ministry of Healthcare of Russian Federation, St. Petersburg, Russia.
Institute of Experimental Medicine, Almazov National Medical Research Centre, Ministry of Healthcare of Russian Federation, St. Petersburg, Russia.
Lab Anim (NY). 2025 May;54(5):126-132. doi: 10.1038/s41684-025-01545-0. Epub 2025 Apr 30.
The small teleost zebrafish (Danio rerio) has become a critically important laboratory animal in biomedicine. One of their key practical advantages, the convenient method of small-molecule administration via water immersion, has certain problems with dosing precision and drug delivery. Here, we present a simple protocol for the intranasal delivery of neuroactive drugs in adult zebrafish using arecoline and nicotine, two well-studied reference neuroactive drugs chosen for the proof of concept. Adult fish received 1 μL water solution of arecoline (1 and 10 mg/mL) or nicotine tartrate (5 and 10 mg/mL) or the same volume of drug-free water (control) into both nostrils, followed by behavioral testing in the novel tank test 5 min later. Mass spectrometry analyses confirmed that both drugs rapidly reached the zebrafish brain following intranasal administration. Intranasally administered arecoline (10 mg/mL) and nicotine (5 and 10 mg/mL) demonstrated overt behavioral profiles, evoking characteristic anxiolytic-like effects in zebrafish similar to those observed here for a standard 20-min water immersion method (10 mg/L arecoline or 30 mg/L nicotine). Overall, we showed that neuroactive drugs can be delivered to adult zebrafish intranasally to exert central effects, which may (at least for some drugs) occur faster and can need smaller drug quantities than for the water immersion delivery.
小型硬骨鱼斑马鱼(Danio rerio)已成为生物医学领域极为重要的实验动物。它们的一个关键实际优势,即通过水浸法方便地给予小分子药物,但在给药精度和药物递送方面存在一定问题。在此,我们提出了一种简单的方案,用于在成年斑马鱼中通过鼻腔递送神经活性药物,使用槟榔碱和尼古丁,这两种经过充分研究的参考神经活性药物用于概念验证。成年鱼每个鼻孔接受1微升槟榔碱(1和10毫克/毫升)或酒石酸尼古丁(5和10毫克/毫升)的水溶液或相同体积的无药水溶液(对照),5分钟后在新水箱试验中进行行为测试。质谱分析证实,两种药物经鼻腔给药后迅速到达斑马鱼大脑。经鼻腔给药的槟榔碱(10毫克/毫升)和尼古丁(5和10毫克/毫升)表现出明显的行为特征,在斑马鱼中引起特征性的抗焦虑样效应,类似于在此观察到的标准20分钟水浸法(10毫克/升槟榔碱或30毫克/升尼古丁)的效应。总体而言,我们表明神经活性药物可以经鼻腔递送至成年斑马鱼以发挥中枢作用,这可能(至少对于某些药物而言)比水浸递送起效更快且所需药物量更小。