Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2014615 | Pharmacology Biochemistry and Behavior | 2006 | 7 Pages |
Oral administration of a MeOH–CH2Cl2 (1:1) extract of the stem bark of Hintonia standleyana (HSE) produced a dose-dependent antinociceptive effect when tested in mice using the writhing (150–750 mg/kg) and the hot-plate (150–600 mg/kg) models. From the active extract 3-O-β-d-glucopyranosyl-23,24-dihydrocucurbitacin F (GDHCF), 5-O-[β-d-apiofuranosyl-(1→6)-β-d-glucopyranosyl]-7-methoxy-3′,4′-dihydroxy-4-phenylcoumarin (AG4-PC) and desoxycordifolinic acid (DCA) were isolated. GDHCF (10–100 mg/kg, p.o.) significantly reduced acetic acid-induced abdominal contortions and increased the hot-plate latency in comparison to vehicle-treated mice. Metamizol (50–100 mg/kg) and morphine (2.5–5 mg/kg) were used as positive controls, respectively. GDHCF-induced antinociception was partially blocked by naloxone (1 mg/kg, i.p.), l-NAME (150 mg/kg, i.p.) and glibenclamide (10 mg/kg, i.p.) suggesting that its pharmacological effect could be due to the activation of the nitric oxide pathway, followed by the opening of the ATP-sensitive K+ channels, as well as an activation of the opioid receptors.