Pharmacokinetic Study in Mice of Galphimine-A, an Anxiolytic Compound from Galphimia glauca
AbstractThe aim of this study was to obtain pharmacokinetic data for the anxiolytic compound galphimine-A (G–A) from Galphimia glauca. G–A is the most abundant anxiolytic compound in this plant, while Galphimine-E (G–E) is the most abundant galphimine, but inactive. G–E was transformed chemically into G–A. The pharmacokinetic study was carried out in ICR mice, which were orally administered a single 200 mg/kg dose of G–A. Samples of blood and brain were taken at different times after administration of G–A. Previously, we established the validation of methods for determining the concentration of G–A. The G–A was detected in plasma 5 min after oral administration, and its concentration reached 2.47 μg/mL. Data from concentration-time curves allowed us to establish the main pharmacokinetic parameters in two models: one- and/or two-compartment. Cmax values were 3.33 and 3.42 μg/mL respectively, likewise AUC0→1440 min were 1,951.58 and 1,824.95 μg/mL·min. The G–A in brain tissue was noted to cross the blood-brain barrier, reaching Cmax 2.74 μg/mL, Tmax 81.6 min, and then drop gradually to 0.32 μg/mL detected at 24 h. The presence of G–A in brain tissue, confirmed that this anxiolytic compound can access the target organ and acts directly on the CNS.
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Vargas, R.A.; Zamilpa, A.; Aguilar, F.A.; Herrera-Ruiz, M.; Tortoriello, J.; Jiménez-Ferrer, E. Pharmacokinetic Study in Mice of Galphimine-A, an Anxiolytic Compound from Galphimia glauca. Molecules 2014, 19, 3120-3134.
Vargas RA, Zamilpa A, Aguilar FA, Herrera-Ruiz M, Tortoriello J, Jiménez-Ferrer E. Pharmacokinetic Study in Mice of Galphimine-A, an Anxiolytic Compound from Galphimia glauca. Molecules. 2014; 19(3):3120-3134.Chicago/Turabian Style
Vargas, Rodolfo A.; Zamilpa, Alejandro; Aguilar, Francisco A.; Herrera-Ruiz, Maribel; Tortoriello, Jaime; Jiménez-Ferrer, Enrique. 2014. "Pharmacokinetic Study in Mice of Galphimine-A, an Anxiolytic Compound from Galphimia glauca." Molecules 19, no. 3: 3120-3134.