In Silico Screening Identification of Fatty Acids and Fatty Acid Derivatives with Antiseizure Activity: In Vitro and In Vivo Validation

Author:

Barrionuevo Emilia Mercedes12,Peralta Estefanía12,Manzur De Nardi Agustín3ORCID,Monat Juliana3ORCID,Fallico Maximiliano José12,Llanos Manuel Augusto12,Gavernet Luciana12ORCID,Mustafá Emilio Román4,Martin Pedro3,Talevi Alan12

Affiliation:

1. Laboratory of Bioactive Compound Research and Development (LIDeB), Faculty of Exact Sciences, National University of La Plata (UNLP), Blvd. 120 1489, La Plata 1900, Argentina

2. Argentinean National Council of Scientific and Technical Research (CONICET), CCT La Plata, La Plata 1900, Argentina

3. Instituto de Estudios Inmunológicos y Fisiopatológicos (IIFP), Universidad Nacional de La Plata–CICPBA–CONICET, Boulevard 120 no. 1489, La Plata 1900, Argentina

4. Electrophysiology Laboratory of the Multidisciplinary Institute of Cell Biology [Argentine Research Council (CONICET), Scientific Research Commission of the Province of Buenos Aires (CIC-PBA) and National University of La Plata (UNLP)], La Plata 1900, Argentina

Abstract

High fat diets have been used as complementary treatments for seizure disorders for more than a century. Moreover, many fatty acids and derivatives, including the broad-spectrum antiseizure medication valproic acid, have been explored and used as pharmacological agents to treat epilepsy. In this work, we have explored the anticonvulsant potential of a large library of fatty acids and fatty acid derivatives, the LIPID MAPS Structure Database, using structure-based virtual screening to assess their ability to block the voltage-gated sodium channel 1.2 (NaV1.2), a validated target for antiseizure medications. Four of the resulting in silico hits were submitted for experimental confirmation using in vitro patch clamp experiments, and their protective role was evaluated in an acute mice seizure model, the Maximal Electroshock seizure model. These four compounds were found to protect mice against seizures. Two of them exhibited blocking effects on NaV1.2, CaV2.2, and CaV3.1.

Funder

ANPCyT

Universidad Nacional de La Plata

ApoyoDravet’s INDRE

Publisher

MDPI AG

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4. Recent advances in pharmacotherapy for epilepsy;Pong;Curr. Opin. Neurol.,2023

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