Artigo Produção Nacional Revisado por pares

Chalcones reverse the anxiety and convulsive behavior of adult zebrafish

2021; Elsevier BV; Volume: 117; Linguagem: Inglês

10.1016/j.yebeh.2021.107881

ISSN

1525-5069

Autores

Maria Kueirislene Amâncio Ferreira, Antônio Wlisses da Silva, Atilano Lucas dos Santos Moura, Ketelly Vanessa Barros Sales, Emanuelle Machado Marinho, Joyce do Nascimento Martins Cardoso, Márcia Machado Marinho, Paulo Nogueira Bandeira, Francisco Ernani Alves Magalhães, Emmanuel Silva Marinho, Jane Eire Silva Alencar de Menezes, Hélcio Silva dos Santos,

Tópico(s)

Nicotinic Acetylcholine Receptors Study

Resumo

In the treatment of anxiety and seizures, drugs of the benzodiazepine (BZD) class are used, which act on the Central Nervous System (CNS) through the neurotransmitter gamma-aminobutyric acid (GABA). Flavonoids modulate GABAA receptors. The aim of this study was to evaluate the anxiolytic and anticonvulsant effects of synthetic chalcones and their mechanisms of action via the GABAergic system, using adult zebrafish (ZFa). The animals were treated with chalcones (4.0 or 20 or 40 mg/kg; 20 µL; i.p) and submitted to the open field and 96 h toxicity test. Chalcones that cause locomotor alteration were evaluated in the light and dark anxiolytic test. The same doses of chalcones were evaluated in the anticonvulsant test. The lowest effective dose was chosen to assess the possible involvement in the GABAA receptor by blocking the flumazenil (fmz) antagonist. No chalcone was toxic and altered ZFa’s locomotion. All chalcones had anxiolytic and anticonvulsant effects, mainly chalcones 1, where all doses showed effects in both tests. These effects were blocked by Fmz (antagonist GABAA), where it shows evidence of the performance of these activities of the GABA system. Therefore, this study demonstrated in relation to structure–activity, that the position of the substituents is important in the intensity of activities and that the absence of toxicity and the action of these compounds in the CNS, shows the pharmacological potential of these molecules, and, therefore, the insights are designed for the development of new drugs.

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