Molecular Docking and GC/MS‐Based Approach for Identification of Anxiolytic Alkaloids from Griffinia (Amaryllidaceae) Species in a Zebrafish Model

• Published in: Chemistry & biodiversity 2024-03, Vol.21 (3), p.e202302122-n/a
• Main Authors: Leite, Elder Luis Lima, Sheila de Queiroz Souza, Ana, Riceli Vasconcelos Ribeiro, Paulo, Cássia Alves Pereira, Rita, Florêncio Martins, Natália, Kueirislene Amâncio Ferreira, Maria, Silva Alencar de Menezes, Jane Eire, Silva dos Santos, Hélcio, Deusdênia Loiola Pessoa, Otília, Marques Canuto, Kirley
• Format: Article
• Language: English
• Subjects: Alkaloids; anxiety; Benzodiazepines; Danio rerio; Diazepam; Gas chromatography; Griffinia; In vivo methods and tests; lycorine; Mass spectrometry; Mass spectroscopy; Molecular docking; Receptors; Serotonin receptors; Tropical environment; Tropical environments; Zebrafish; γ-Aminobutyric acid
• ISSN: 1612-1872; 1612-1880
• DOI: 10.1002/cbdv.202302122

Griffinia gardneriana Ravenna, Griffinia liboniana Morren and Griffinia nocturna Ravenna (Amarillydaceae) are bulbous plants found in tropical regions of Brazil. Our work aimed to determine the alkaloid profiles of Griffinia spp. and evaluate their anxiolytic potential through in vivo and in silico assays. The plants grown in greenhouses were dried and their ground bulbs were subjected to liquid‐liquid partitions, resulting in alkaloid fractions that were analyzed by gas chromatography coupled to mass spectrometry (GC‐MS). Anxiolytic activity was evaluated in zebrafish (Danio rerio) through intraperitoneal injection at doses of 40, 100 and 200 mg/kg in light‐dark box test. GC‐MS analyses revealed 23 alkaloids belonging to different skeleton types: lycorine, homolychorine, galanthamine, crinine, haemanthamine, montanine and narcisclasine. The chemical profiles were relatively similar, presenting 8 alkaloids common to the three species. The major component for G. gardneriana and G. liboniana was lycorine, while G. nocturna consisted mainly of anhydrolycorine. All three alkaloid fractions demonstrated anxiolytic effect. Furthermore, pre‐treatment with diazepam and pizotifen drugs was able to reverse the anxiolytic action, indicating involving the GABAergic and serotonergic receptors. Molecular docking showed that the compounds vittatine, lycorine and 11,12‐dehydro‐2‐methoxyassoanine had high affinity with both receptors, suggesting them to be responsible for the anxiolytic effect.