Larissa Rodrigues Jales Martins1,2, Nadia Eligia Nunes Pinto Paracampo3, Paulo Riceli Vasconcelos Ribeiro2, Hélcio Silva dos Santos1, Jane Eire Silva Alencar de Menezes1, Amanda Maria Barros Alves1, Kirley Marques Canuto2
Simira paraensis, commonly known as araribá-rosa, is a small tree native to northern, northeastern, and central-western regions of Brazil. It is notable for producing a red pigment traditionally used as a natural food coloring. Phytochemical studies of the Simira genus highlight the predominance of beta-carbonyl indole alkaloids, compounds known for their effects on the central nervous system. However, scientific data on S. paraensis remain scarce or unavailable. This study employed a metabolomic approach to characterize the chemical profile and assess the anxiolytic potential of S. paraensis bark. The powdered bark was extracted via ultrasound-assisted extraction using methanol (pH = 2) for 2 hours, yielding a red extract (SP-BME) after solvent removal. Dereplication analysis was performed using Ultra-Performance Liquid Chromatography with Electrospray Ionization coupled to Quadrupole and Time-of-Flight Mass Spectrometry (UPLC-ESI-QToF-MS/MS) in both positive and negative ionization modes. Anxiolytic activity was evaluated in zebrafish using the light/dark test following oral administration of the extract (20 µL) at doses of 40, 200, and 400 mg kg-1. Diazepam (4 mg kg-1) and 3% DMSO were used as positive and negative controls, respectively. To assess GABAergic involvement, fish were pretreated with flumazenil (4 mg kg-1) prior to testing. The UPLC-ESI-QToF-MS/MS analysis of SP-BME revealed 21 peaks tentatively identified as beta-carbonyl indole alkaloids, along with phenolic acids, their derivatives, and iridoids. The extract exhibited significant anxiolytic effects at all tested concentrations, which appeared to be mediated via the GABAA receptor. These results suggest that S. paraensis shares phytochemical similarities with other Simira species and that its anxiolytic activity is likely due to the presence of beta-carbonyl indole alkaloids. The findings highlight S. paraensis as a promising natural source of bioactive colorants with potential pharmacological applications.
Agradecimentos: EMBRAPA, Funcap