Tropane Alkaloid Isolated from Erythroxylum bezerrae Exhibits Neuropharmacological Potential in an Adult Zebrafish (Danio rerio) Model

Author:

Ribeiro Liberato Hortência1,Bezerra Maciel Jéssica1,Wlisses Da Silva Antônio2,Freitas da Silva Ana Eloysa1,San De Oliveira Brito Luana3,Silva Jacilene1,Sydney Henrique da Silva Francisco4,Bezerra Arnaldo S.5,Kuerislene Amâncio Ferreira Maria1,Machado Marinho Marcia6,Silva Marinho Gabrielle1,Deusdênia Loiola Pessoa Otília3,Goberlânio De Barros Silva Paulo7,Noronha Coelho‐de‐souza Andrelina4,Florindo Guedes Izabel5,Ferreira de Castro Gomes Andreia8,Eire Silva Alencar De Menezes Jane1,Silva Santos Hélcio16

Affiliation:

1. Programa de PósGraduação em Ciências Naturais Universidade Estadual do Ceará Fortaleza Ceará Brazil

2. Rede Nordeste de Biotecnologia Universidade Estadual do Ceará Fortaleza Ceará Brazil

3. Departamento de Química Orgânica e Inorgânica Universidade Federal do Ceará Campus do Pici s/n Fortaleza Ceará Brazil

4. Centro de Ciências da Saúde Universidade Estadual do Ceará Fortaleza Ceará Brazil

5. Programa de PósGraduação em Ciências Fisiológicas Universidade Estadual do Ceará

6. Universidade Estadual do Vale do Acaraú Centro de Ciências Exatas e Tecnologia Sobral Ceará Brasil

7. Programa de PósGraduação em Odontologia Centro Universitário Unichristus Fortaleza Ceará Brazil

8. Centro de Biologia Molecular e Ambiental Universidade do Minho Escola de Ciências, Departamento de Biologia Braga Portugal

Abstract

AbstractThis study carried out to investigate the anti‐inflammatory and antinociceptive effect of tropane alkaloid (EB7) isolated from E. bezerrae. It evaluated the toxicity and possible involvement of ion channels in the antinociceptive effect of EB7, as well as its anti‐inflammatory effect in adult zebrafish (Zfa). Docking studies with EB7 and COX‐1 and 2 were also performed. The tested doses of EB7 (4, 20 and 40 mg/kg) did not show any toxic effect on Zfa during the 96h of analysis (LD50>40 mg/kg). They did not produce any alteration in the locomotor behavior of the animals. Furthermore, EB7 showed promising pharmacological effects as it prevented the nociceptive behavior induced by hypertonic saline, capsaicin, formalin and acid saline. EB7 had its analgesic effect blocked by amiloride involving the neuromodulation of ASICs in Zfa. In evaluating the anti‐inflammatory activity, the edema induced by κ‐carrageenan 3.5 % was reduced by the dose of 40 mg/kg of EB7 observed after the fourth hour of analysis, indicating an effect similar to that of ibuprofen. Molecular docking results indicated that EB7 exhibited better affinity energy when compared to ibuprofen control against the two evaluated targets binding at different sites in the cocrystallized COX‐1 and 2 inhibitors.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Wiley

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