Department of Animal Physiology and Pharmacology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, PL 20-033 Lublin, Poland.
Department of Animal Physiology and Pharmacology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, PL 20-033 Lublin, Poland.
Toxicol Appl Pharmacol. 2021 Sep 15;427:115655. doi: 10.1016/j.taap.2021.115655. Epub 2021 Jul 27.
Several studies with larvae and adult zebrafish have shown that old and new antiseizure drugs (ASDs) produce discrepant results in seizure tests, locomotor activity or anxiety models. In this study, the pentylenetetrazole seizure test (PTZ) was performed to assess the effectiveness of four new ASDs: lamotrigine (LTG), topiramate (TPM), felbamate (FBM), and levetiracetam (LEV) in the subsequent stages of seizures in adult fish. All ASDs were administered intraperitoneally (i.p.). The time of maximal anticonvulsant effect and the dose-response relationship of the drugs were assessed. The effects of studied ASDs on the locomotor activity and the anxiety-like behavior in the color preference test were also investigated. Furthermore, drug concentrations in zebrafish homogenates were determined. LTG, TPM, and LEV significantly increased the seizure latency at three subsequent stages of seizures (SI-SIII), while FBM was effective only at SI. Locomotor activity decreased after TPM treatment. TPM and FBM exhibited a strong anxiolytic-like effect in the color preference test. LEV at the highest dose tested had a weak anxiolytic-like effect. The HPLC analysis showed average concentrations of the studied ASDs in the fish body during their maximum anticonvulsant activity. The present study shows that FBM cannot inhibit all subsequent PTZ seizure stages in the adult fish. Except for LTG, the studied drugs affected the anxiety-like behavior of treated animals. Furthermore, only TPM significantly changed locomotion parameters. Our findings support the need to accurately characterize the efficacy of new ASDs at different stages of the PTZ-induced seizures in adult zebrafish.
几项针对幼虫和成年斑马鱼的研究表明,旧的和新的抗癫痫药物(ASD)在癫痫发作测试、运动活动或焦虑模型中产生了不一致的结果。在这项研究中,戊四氮惊厥测试(PTZ)用于评估四种新的 ASD 的有效性:拉莫三嗪(LTG)、托吡酯(TPM)、非氨酯(FBM)和左乙拉西坦(LEV)在成年鱼的后续癫痫发作阶段。所有 ASD 均通过腹腔内(i.p.)给药。评估了药物的最大抗惊厥作用时间和剂量反应关系。还研究了研究中的 ASD 对运动活动和颜色偏好测试中焦虑样行为的影响。此外,还测定了斑马鱼匀浆中的药物浓度。LTG、TPM 和 LEV 显著增加了三个后续癫痫发作阶段(SI-SIII)的癫痫发作潜伏期,而 FBM 仅在 SI 有效。TPM 治疗后运动活动减少。TPM 和 FBM 在颜色偏好测试中表现出强烈的抗焦虑样作用。在测试的最高剂量下,LEV 具有微弱的抗焦虑样作用。HPLC 分析显示了研究中的 ASD 在其最大抗惊厥活性期间在鱼体中的平均浓度。本研究表明,FBM 不能抑制成年鱼中所有随后的 PTZ 癫痫发作阶段。除了 LTG 之外,研究的药物还影响了治疗动物的焦虑样行为。此外,只有 TPM 显著改变了运动参数。我们的研究结果支持需要在成年斑马鱼的 PTZ 诱导的癫痫发作的不同阶段准确描述新的 ASD 的疗效。