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Evaluation of the neuropharmacological effects of Gardenin A in mice.
Alonso-Castro, Angel J; Gasca-Martínez, Deisy; Cortez-Mendoza, Laura V; Alba-Betancourt, Clara; Ruiz-Padilla, Alan J; Zapata-Morales, Juan R.
Affiliation
  • Alonso-Castro AJ; Departamento de Farmacia, División de Ciencias Naturales y Exactas, Universidad de Guanajuato, Guanajuato, Guanajuato, Mexico.
  • Gasca-Martínez D; Instituto de Neurobiología, Universidad Nacional Autónoma de México, Juriquilla, Querétaro, Mexico.
  • Cortez-Mendoza LV; Instituto de Neurobiología, Universidad Nacional Autónoma de México, Juriquilla, Querétaro, Mexico.
  • Alba-Betancourt C; Departamento de Farmacia, División de Ciencias Naturales y Exactas, Universidad de Guanajuato, Guanajuato, Guanajuato, Mexico.
  • Ruiz-Padilla AJ; Departamento de Farmacia, División de Ciencias Naturales y Exactas, Universidad de Guanajuato, Guanajuato, Guanajuato, Mexico.
  • Zapata-Morales JR; Departamento de Farmacia, División de Ciencias Naturales y Exactas, Universidad de Guanajuato, Guanajuato, Guanajuato, Mexico.
Drug Dev Res ; 81(5): 600-608, 2020 08.
Article in En | MEDLINE | ID: mdl-32181517
This work describes the neuropharmacological (sedative, anxiolytic, antidepressant, and anticonvulsant) actions of Gardenin A (GA) (0.1-25 mg/kg p.o.), a flavonoid found in medicinal plants. The sedative effects of GA were assessed with the pentobarbital-induced sleep test. The anxiolytic actions of GA were evaluated with the elevated plus-maze, the light-dark box test, the exploratory cylinder assay, and the open field test. Motor coordination was evaluated with the rotarod test and the open field test. The antidepressant-like actions of GA were evaluated with the tail suspension test and forced swimming test. The mechanisms of the anxiolytic-like and antidepressant-like effects of GA were assessed using inhibitors of neurotransmission pathways. The anticonvulsant activity of GA was evaluated with the strychnine-induced seizure test. The sedative effects of GA were evident only at a dose of 25 mg/kg, which increased the duration of sleep but did not alter sleep onset. GA showed anxiolytic-like actions with activity comparable to that of clonazepam in all experimental tests. The GABAA receptor antagonist bicuculline reversed the anxiolytic-like effects of GA. Furthermore, GA showed significant antidepressant-like actions in both models with activity comparable to that of fluoxetine. Yohimbine, an α2-adrenoceptor blocker, inhibited the antidepressant-like actions of GA. In addition, GA (1-10 mg/kg) did not affect locomotor coordination in mice and delayed the onset of convulsions. These findings suggest that GA induces anxiolytic-like effects and has anticonvulsant actions by the possible involvement of the GABAergic system. The antidepressant-like actions of GA may be mediated by noradrenergic neurotransmission.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Seizures / Anti-Anxiety Agents / Flavones / Hypnotics and Sedatives / Anticonvulsants / Antidepressive Agents Type of study: Prognostic_studies Limits: Animals Language: En Journal: Drug Dev Res Year: 2020 Document type: Article Affiliation country: Mexico Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Seizures / Anti-Anxiety Agents / Flavones / Hypnotics and Sedatives / Anticonvulsants / Antidepressive Agents Type of study: Prognostic_studies Limits: Animals Language: En Journal: Drug Dev Res Year: 2020 Document type: Article Affiliation country: Mexico Country of publication: United States