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Neuropharmacological Effects of the Dichloromethane Extract from the Stems of Argemone ochroleuca Sweet (Papaveraceae) and Its Active Compound Dihydrosanguinarine

Argemone ochroleuca Sweet (Papaveraceae) is used in folk medicine as a sedative and hypnotic agent. This study aimed to evaluate the anxiolytic-like, sedative, antidepressant-like, and anticonvulsant activities of a dichloromethane extract of A. ochroleuca stems (AOE), chemically standardized using...

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Detalles Bibliográficos
Autores principales: Yáñez-Barrientos, Eunice, Barragan-Galvez, Juan Carlos, Hidalgo-Figueroa, Sergio, Reyes-Luna, Alfonso, Gonzalez-Rivera, Maria L., Cruz Cruz, David, Isiordia-Espinoza, Mario Alberto, Deveze-Álvarez, Martha Alicia, Villegas Gómez, Clarisa, Alonso-Castro, Angel Josabad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10459336/
https://www.ncbi.nlm.nih.gov/pubmed/37631090
http://dx.doi.org/10.3390/ph16081175
Descripción
Sumario:Argemone ochroleuca Sweet (Papaveraceae) is used in folk medicine as a sedative and hypnotic agent. This study aimed to evaluate the anxiolytic-like, sedative, antidepressant-like, and anticonvulsant activities of a dichloromethane extract of A. ochroleuca stems (AOE), chemically standardized using gas chromatography–mass spectrometry (GC–MS), and its active compound dihydrosanguinarine (DHS). The anxiolytic-like, sedative, antidepressant-like, and anticonvulsant activities of the AOE (0.1–50 mg/kg p.o.) and DHS (0.1–10 mg/kg p.o.) were evaluated using murine models. A possible mechanism for the neurological actions induced by the AOE or DHS was assessed using inhibitors of neurotransmission pathways and molecular docking. Effective dose 50 (ED(50)) values were calculated by a linear regression analysis. The AOE showed anxiolytic-like activity in the cylinder exploratory test (ED(50) = 33 mg/kg), and antidepressant-like effects in the forced swimming test (ED(50) = 3 mg/kg) and the tail suspension test (ED(50) = 23 mg/kg), whereas DHS showed anxiolytic-like activity (ED(50) = 2 mg/kg) in the hole board test. The AOE (1–50 mg/kg) showed no locomotive affectations or sedation in mice. A docking study revealed the affinity of DHS for α2-adrenoreceptors and GABA(A) receptors. The anxiolytic-like and anticonvulsant effects of the AOE are due to GABAergic participation, whereas the antidepressant-like effects of the AOE are due to the noradrenergic system. The noradrenergic and GABAergic systems are involved in the anxiolytic-like actions of DHS.