Part Used : ไม่ระบุ
Activity : EFFECTS ON PHARMACOKINETIC
Solvent/Active Compound : Ginkgolide B (GB)
Type of experiment : in vivo
Type of animal : rat
N(Total) : -
N(Treatment) : -
Route : Intravenous
Dose/Conc.(herb) : 10 mg/kg
Duration : -
Type of interaction : Pharmacokinetics
Interaction with drug : Probenecid*/Benemid
Dose/Conc.(drug) : 300 mg/kg
Remark : The systemic exposure in the group treated with probenecid (p<0.05 vs control) was significantly raised to 14.75+/-1.328 microgram/mL/h. Specifically, probenecid could significantly decreased the CLtotal of GB from 1.17+/-0.331 to 0.596+/-0.0573 L/h/kg. Albeit probenecid could significantly reduce GB clearance and volume of distribution (V) when compared with control group, the elimination half-time (t1/2lambda) of each group remained close to each other, fitted as 2.04+/-0.376, and 2.34+/-0.851, for the control and probenecid, respectively.
Note : CLtotal = total plasma clearance