GABAA receptor participation in anxiolytic and anticonvulsant effects of (E)-3-(furan-2-yl)-1-(2hydroxy-3,4,6-trimethoxyphenyl)prop-2-en-1-one in adult zebrafish

• Published in: Neurochemistry international 2022-05, Vol.155, p.105303-105303, Article 105303
• Main Authors: Silva Mendes, Francisco Rogênio, Wlisses da Silva, Antonio, Amâncio Ferreira, Maria Kueirislene, de Lima Rebouças, Emanuela, Marinho, Emanuelle Machado, Marinho, Márcia Machado, Bandeira, Paulo Nogueira, Rodrigues Teixeira, Alexandre Magno, Silva Alencar de Menezes, Jane Eire, Alves de Siqueira, Erlania, Róseo Paula Pessoa Bezerra de Menezes, Ramon, Marinho, Emmanuel Silva, Silva dos Santos, Hélcio
• Format: Article
• Language: English
• Subjects: Anxiolytic effect; Benzodiazepines; Convulsion; Zebrafish
• ISSN: 0197-0186; 1872-9754
• DOI: 10.1016/j.neuint.2022.105303

Anxiety is a mental disorder that affects 25% of patients with epilepsy, and treatments for anxiety and seizures involve the use of benzodiazepines, a class of drugs that have many adverse effects such as decreased motor coordination, drowsiness, and sedation. Thus, new types of drugs with minimal side effects are of immediate requirement. Chalcones comprise a class of compounds with important therapeutic potential and have recently been investigated for their potential as anxiolytic and anticonvulsant agents. Therefore, this study aimed to evaluate the anxiolytic and anticonvulsant effects of the synthetic chalcone (E)-3-(furan-2-yl)-1-(2hydroxy-3,4,6-trimethoxyphenyl)prop-2-en-1-one (FURCHAL) using adult zebrafish as an animal model. Anxiolytic potential was assessed using the light/dark test and the anticonvulsant effect in 3-stage pentylenetetrazol (PTZ)-induced seizure tests. The mechanisms of the anxiolytic effect were analyzed using γ-aminobutyric acid (GABA) and the serotoninergic system. The anxiolytic effect of FURCHAL was verified by a reduction in fish locomotion, similar to diazepam (DZP), which may involve the GABAA receptor, as there was no reversal in the anxiolytic behavior of animals treated with FURCHAL by serotonergic antagonists. In addition, pretreatment with flumazenil blocked the anticonvulsant effect of FURCHAL and DZP at all three stages, indicating that FURCHAL also has anticonvulsant effects and that the presence of the α,β unsaturated aromatic system and heterocyclic moiety in FURCHAL provided greater affinity for the GABAA receptors. Molecular docking revealed that the interactions involved in the formation of the protein-binding complex FURCHAL-GABAA are formed by three H-bonds involving the oxygen atoms of FURCHAL, and notably, complexes operated in the same region of the DZP site. Thus, this study adds new evidence and highlights that FURCHAL can potentially be used to develop compounds with anxiolytic and anticonvulsant properties. [Display omitted] •A chalcone FURCHAL was synthesized by Claisen-Schmidt condensation reaction.•The structure of the chalcone FURCHAL was determined by spectroscopic data.•Anxiolytic and anticonvulsant effect of chalcone FURCHAL were made in adult zebrafish.•Anticonvulsant effect of chalcone FURCHAL may involve GABAergic neuromodulation.•Molecular docking studies were carried out.