Čes. slov. farm. 2025, 74(2):E1-E8 | DOI: 10.36290/csf.2025.021

Anticonvulsant biotargets of digoxin: in silico study and in vivo verification

Vadym Tsyvunin¹, Hanna Severina², Sergii Shtrygol’¹, Victoriya Georgiyants², Diana Shtrygol’³

¹ Department of Pharmacology and Clinical Pharmacy, National University of Pharmacy, Ukraine

² Department of Pharmaceutical Chemistry, National University of Pharmacy, Ukraine

³ Department of Neurology, Psychiatry, Narcology and Medical Psychology, School of Medicine, V. N. Karazin Kharkiv National University, Ukraine

One of the promising ways to control multidrug-resistant epilepsy may be to use, in addition to traditional antiepileptic drugs (AEDs), medicines from other pharmacological groups – the so-called „non-antiepileptic” drugs. Among such drugs, the cardiac glycoside digoxin deserves special attention. It was established that sub-cardiotonic doses of digoxin exhibit both their own anticonvulsant effect and have been shown to enhance the anticonvulsant potential of classical AEDs. However, the mechanisms of this action and the probable cerebral biotargets with which these properties of digoxin may be associated, remain completely unknown. Molecular docking of digoxin to the following cerebral biotargets was performed: GABAAR, GlyR, mGluR5, AMPAR, hBCATc, mGlu8R, NMDA-GluN1, KCNQ2, COX-1 and COX-2. To confirm the in silico results in vivo pharmacological studies under conditions of acute bicuculline-induced seizures and pentylenetetrazole kindling in mice have been carried out. It was established that digoxin shows high affinity to GABAergic biotargets and an identical to retigabine affinity to voltage-gated potassium channels KCNQ2 in silico. In vivo results fully confirm the established by molecular docking GABAergic properties of the cardiac glycoside: digoxin provides a potent anticonvulsant activity on the model of acute primary generalized bicuculline-induced seizures and a moderate anticonvulsant effect under pentylenetetrazole kindling. At the same time, the ability of digoxin to maximally enhance the anticonvulsant potential of sodium valproate has been revealed. Thus, it has been proven that the anticonvulsant properties of digoxin are most likely related to the ability to enhance the inhibitory properties of GABA and GABAergic agents.

Keywords: digoxin, anticonvulsant activity, molecular targets, docking, experimental seizures

Accepted: June 6, 2025; Published: June 18, 2025  Show citation