Institute of Medical Psychology and Behavioral Immunobiology, Center for Translational Neuro-Behavioral Sciences (C-TNBS), University Medicine Essen, University Duisburg-Essen, Essen, Germany.
Department of Infectious Diseases, West German Centre of Infectious Diseases, University Medicine Essen, University Duisburg-Essen, Essen, Germany.
Brain Behav. 2024 Nov;14(11):e70146. doi: 10.1002/brb3.70146.
Studies in experimental animals revealed that acute and chronic treatment with small-molecule immunosuppressive drugs lead to neurobehavioral alterations in rodents.
Against this background, this study investigated behavioral alterations in rats after repeated administration of FTY720, an immunosuppressive drug used for the treatment of multiple sclerosis, employing the open field, elevated plus maze, and dark/light tests.
Compared to controls, repeated FTY720 treatment affected behavior in rats, reflected by a reduction in distance traveled as well as increased time engaged in freezing in the open field and elevated plus maze. Furthermore, the time spent freezing in the elevated plus maze test positively correlated with FTY720 concentrations in the amygdala and insular cortex, two brain regions involved in regulation of emotionality. Since no changes in plasma corticosterone levels were observed, stress effects due to treatment, behavioral testing, or handling can be ruled out.
The present findings indicate that treatment with FTY720 did not induce typical anxiety-like behavioral patterns in otherwise healthy rats as seen following treatment with other immunosuppressive drugs. Nevertheless, it remains of great importance to evaluate behavioral effects in clinical practice to shed more light onto possible detrimental side effects emerging during treatment with small-molecule immunosuppressive drugs.
实验动物研究表明,小分子免疫抑制剂的急性和慢性治疗会导致啮齿动物的神经行为改变。
在此背景下,本研究采用旷场、高架十字迷宫和明暗箱测试,调查了重复给予用于治疗多发性硬化症的免疫抑制剂 FTY720 后大鼠的行为改变。
与对照组相比,重复 FTY720 处理影响了大鼠的行为,表现在旷场和高架十字迷宫中行走距离减少以及冻结时间增加。此外,高架十字迷宫测试中的冻结时间与杏仁核和岛叶皮质中的 FTY720 浓度呈正相关,这两个脑区参与情绪调节。由于未观察到血浆皮质酮水平的变化,因此可以排除由于处理、行为测试或处理引起的应激效应。
本研究结果表明,FTY720 治疗不会在其他健康大鼠中引起类似焦虑的行为模式,如其他免疫抑制剂治疗后所见。然而,在临床实践中评估行为效应仍然非常重要,以便更清楚地了解小分子免疫抑制剂治疗期间出现的可能有害的副作用。