Literature DB >> 27702668

Influence of xanthotoxin (8-methoxypsoralen) on the anticonvulsant activity of various novel antiepileptic drugs against maximal electroshock-induced seizures in mice.

Mirosław Zagaja1, Marta Andres-Mach2, Paweł Patrzylas3, Daniel Pyrka4, Monika Szpringer5, Magdalena Florek-Łuszczki6, Dorota Żółkowska7, Krystyna Skalicka-Woźniak8, Jarogniew J Łuszczki9.   

Abstract

The aim of this study was to determine the effects of xanthotoxin (8-methoxypsoralen) on the protective action of 5 various second- and third-generation antiepileptic drugs (i.e., lacosamide, lamotrigine, oxcarbazepine, pregabalin and topiramate) in the mouse maximal electroshock-induced seizure model. Seizure activity was evoked in adult male albino Swiss mice by a current (25mA, 500V, 0.2s stimulus duration) delivered via auricular electrodes. Drug-related adverse effects were determined in the chimney, grip-strength and passive avoidance tests. Total brain antiepileptic drug concentrations were measured to confirm pharmacodynamic nature of observed interactions with xanthotoxin. Results indicate that xanthotoxin (100mg/kg, i.p.) significantly enhanced the anticonvulsant action of lacosamide (P<0.01), oxcarbazepine (P<0.05), pregabalin (P<0.01), and topiramate (P<0.001), but not that of lamotrigine in the maximal electroshock-induced seizure test. Moreover, xanthotoxin (50mg/kg) still significantly potentiated the anticonvulsant action of lacosamide (P<0.05), pregabalin (P<0.05), and topiramate (P<0.001) in this seizure test. Xanthotoxin had no significant impact on total brain concentrations of the studied antiepileptic drugs in mice. Furthermore, combinations of xanthotoxin with oxcarbazepine or topiramate produced no adverse effects. However, xanthotoxin in combination with lacosamide, lamotrigine or pregabalin significantly reduced muscular strength in mice in the grip-strength test. In the chimney test, only the combinations of xanthotoxin with pregabalin significantly impaired motor coordination in mice. In conclusion, the combinations of xanthotoxin with oxcarbazepine and topiramate produce beneficial anticonvulsant pharmacodynamic interactions in the maximal electroshock-induced seizure test. A special caution is advised when combining xanthotoxin with pregabalin due to appearance of acute adverse effects. Copyright Â
© 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Coumarins; Lacosamide (PubChem CID: 219078); Lamotrigine (PubChem CID: 3878); Maximal electroshock-induced seizure test; Novel antiepileptic drugs; Oxcarbazepine (PubChem CID: 34312); Pharmacodynamic interaction; Pregabalin (PubChem CID: 5486971); Topiramate (PubChem CID: 5284627); Xanthotoxin; Xanthotoxin (PubChem CID: 4114)

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Year:  2016        PMID: 27702668     DOI: 10.1016/j.fitote.2016.09.020

Source DB:  PubMed          Journal:  Fitoterapia        ISSN: 0367-326X            Impact factor:   2.882


  4 in total

1.  N-Benzyl-(2,5-dioxopyrrolidin-1-yl)propanamide (AS-1) with Hybrid Structure as a Candidate for a Broad-Spectrum Antiepileptic Drug.

Authors:  Krzysztof Kamiński; Katarzyna Socała; Mirosław Zagaja; Marta Andres-Mach; Michał Abram; Marcin Jakubiec; Mateusz Pieróg; Dorota Nieoczym; Anna Rapacz; Kinga Gawel; Camila V Esguerra; Gniewomir Latacz; Annamaria Lubelska; Bartłomiej Szulczyk; Aleksandra Szewczyk; Jarogniew Jacek Łuszczki; Piotr Wlaź
Journal:  Neurotherapeutics       Date:  2020-01       Impact factor: 7.620

2.  Influence of Umbelliferone on the Anticonvulsant and Neuroprotective Activity of Selected Antiepileptic Drugs: An In Vivo and In Vitro Study.

Authors:  Mirosław Zagaja; Anna Zagaja; Joanna Szala-Rycaj; Aleksandra Szewczyk; Marta Kinga Lemieszek; Grzegorz Raszewski; Marta Andres-Mach
Journal:  Int J Mol Sci       Date:  2022-03-23       Impact factor: 5.923

3.  C-11, a New Antiepileptic Drug Candidate: Evaluation of the Physicochemical Properties and Impact on the Protective Action of Selected Antiepileptic Drugs in the Mouse Maximal Electroshock-Induced Seizure Model.

Authors:  Mirosław Zagaja; Aleksandra Szewczyk; Joanna Szala-Rycaj; Grzegorz Raszewski; Magdalena Chrościńska-Krawczyk; Michał Abram; Krzysztof Kamiński; Marta Andres-Mach
Journal:  Molecules       Date:  2021-05-24       Impact factor: 4.411

4.  Hypertrophic differentiation of mesenchymal stem cells is suppressed by xanthotoxin via the p38‑MAPK/HDAC4 pathway.

Authors:  Zhen Cao; Yun Bai; Chuan Liu; Ce Dou; Jianmei Li; Junyu Xiang; Chunrong Zhao; Zhao Xie; Qiang Xiang; Shiwu Dong
Journal:  Mol Med Rep       Date:  2017-06-29       Impact factor: 2.952

  4 in total

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