Effect of Cinnamaldehyde Chalcone on Behavior in Adult Zebrafish (Danio rerio): In Silico Approach

Author:

Carneiro Romão Ivana1,Costa Siqueira Sônia Maria1,Amâncio Ferreira Maria Kueirislene1,Wlisses da Silva Antonio1,Machado Marinho Márcia23,Ferreira Ribeiro Walber Henrique3,de Castro Gomes Andreia Ferreira4,Alencar de Menezes Jane Eire Silva1,dos Santos Hélcio Silva13

Affiliation:

1. Laboratório de Bioensaios Químicos-Farmacológicos e Ambiental – LabQFAm, Programa de Pós-Graduação em Ciências Naturais Universidade Estadual de Ceará Campus do Itaperi 60714-242 Fortaleza Ceará Brazil

2. Grupo de Química Teórica e Eletroquímica – GQTE Programa de Pós-Graduação em Ciências Naturais, Universidade Estadual de Ceará, Campus do Itaperi, 60714-242, Fortaleza, Ceará, Brazil Programa de Pós-Graduação em Ciências Naturais Universidade Estadual do Ceará Fortaleza Ceará Brazil

3. Curso de Química, Centro de Ciências e Tecnologia, Universidade Estadual do Vale do Acaraú, 62.040-370, Sobral, Ceará, Brazil Curso de Química Universidade Estadual Vale do Acaraú Sobral Ceará Brazil

4. Centre of Molecular and Environmental Biology (CBMA) / Aquatic Research Network (ARNET) Associate Laboratory, Department of Biology, University of Minho, Campus de Gualtar, 4710-057, Braga, Portugal Centro de Biologia Molecular e Ambiental Universidade do Minho Escola de Ciências Departamento de Biologia Braga Portugal

Abstract

AbstractThe study focuses on the anxiolytic potential of chalcone (2E,4E)‐1‐(2‐hydroxyphenyl)‐5‐phenylpenta‐2,4‐dien‐1‐one (CHALCNM) in adult zebrafish. Successfully synthesized in 58 % yield, CHALCNM demonstrated no toxicity after 96 h of exposure. In behavioral tests, CHALCNM (40 mg/kg) reduced locomotor activity and promoted less anxious behavior in zebrafish, confirmed by increased permanence in the light zone of the aquarium. Flumazenil reversed its anxiolytic effect, indicating interaction with GABAA receptors. Furthermore, CHALCNM (4 and 20 mg/kg) preserved zebrafish memory in inhibitory avoidance tests. Virtual screening and ADMET profile studies suggest high oral bioavailability, access to the CNS, favored by low topological polarity (TPSA≤75 Å2) and low incidence of hepatotoxicity, standing out as a promising pharmacological agent against the GABAergic system. In molecular coupling, CHALCNM demonstrated superior affinity to diazepam for the GABAA receptor. These results reinforce the therapeutic potential of CHALCNM in the treatment of anxiety, highlighting its possible future clinical application.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Wiley

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