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| Thai / English name |
Part Used : เหง้าActivity : CYTOCHROME P-450 BINDINGSolvent/Active Compound : red ginseng powderType of experiment : in vivoType of animal : ratType of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : Oral administrationDose/Conc.(herb) : 62.5 mg/kg/dayDuration : 18 hoursType of interaction : PharmacokineticsInteraction with drug : Enflurane*/Methylflurether/Efrane/EthraneDose/Conc.(drug) : -Result : NegativeRemark : Red ginseng extract was dissolved in 0.9% saline (0.5 ml) and administered with 22G gavage needle. rats were dosed 18 hours before administered enflurane 0.6 microliters/g i.p.Note : There were no statistically significant differences in hepatic microsomal cytochrome p-450 content or defluorination of enflurane and methoxyflurane between control and experimental groups using either red ginseng extract or powder.
Part Used : เหง้าActivity : DRUG INTERACTIONSolvent/Active Compound : red ginseng powderType of experiment : in vivoType of animal : ratType of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : Oral administrationDose/Conc.(herb) : 62.5 mg/kg/dayDuration : 18 hoursType of interaction : PharmacokineticsInteraction with drug : Enflurane*/Methylflurether/Efrane/EthraneDose/Conc.(drug) : -Result : NegativeRemark : Red ginseng extract was dissolved in 0.9% saline (0.5 ml) and administered with 22G gavage needle. rats were dosed 18 hours before administered enflurane 0.6 microliters/g i.p.Note : There were no statistically significant differences in hepatic microsomal cytochrome p-450 content or defluorination of enflurane and methoxyflurane between control and experimental groups using either red ginseng extract or powder.
Part Used : เหง้าActivity : DRUG INTERACTIONSolvent/Active Compound : red ginseng powderType of experiment : in vivoType of animal : ratType of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : Oral administrationDose/Conc.(herb) : 125 mg/kg/dayDuration : 18 hoursType of interaction : PharmacokineticsInteraction with drug : Enflurane*/Methylflurether/Efrane/EthraneDose/Conc.(drug) : -Result : NegativeRemark : Red ginseng extract was dissolved in 0.9% saline (0.5 ml) and administered with 22G gavage needle. rats were dosed 18 hours before administered enflurane 0.6 microliters/g i.p.Note : There were no statistically significant differences in hepatic microsomal cytochrome p-450 content or defluorination of enflurane and methoxyflurane between control and experimental groups using either red ginseng extract or powder.
Part Used : เหง้าActivity : CYTOCHROME P-450 BINDINGSolvent/Active Compound : red ginseng powderType of experiment : in vivoType of animal : ratType of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : Oral administrationDose/Conc.(herb) : 125 mg/kg/dayDuration : 18 hoursType of interaction : PharmacokineticsInteraction with drug : Enflurane*/Methylflurether/Efrane/EthraneDose/Conc.(drug) : -Result : NegativeRemark : Red ginseng extract was dissolved in 0.9% saline (0.5 ml) and administered with 22G gavage needle. rats were dosed 18 hours before administered enflurane 0.6 microliters/g i.p.Note : There were no statistically significant differences in hepatic microsomal cytochrome p-450 content or defluorination of enflurane and methoxyflurane between control and experimental groups using either red ginseng extract or powder.
Part Used : เหง้าActivity : DRUG INTERACTIONSolvent/Active Compound : red ginseng powderType of experiment : in vivoType of animal : ratType of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : Oral administrationDose/Conc.(herb) : 125 mg/kg/dayDuration : 18 hoursType of interaction : PharmacokineticsInteraction with drug : Enflurane*/Methylflurether/Efrane/EthraneDose/Conc.(drug) : -Result : NegativeRemark : Red ginseng extract was dissolved in 0.9% saline (0.5 ml) and administered with 22G gavage needle. rats were dosed 18 hours before administered enflurane 0.6 microliters/g i.p.Note : There were no statistically significant differences in hepatic microsomal cytochrome p-450 content or defluorination of enflurane and methoxyflurane between control and experimental groups using either red ginseng extract or powder.
Part Used : เหง้าActivity : CYTOCHROME P-450 BINDINGSolvent/Active Compound : red ginseng powderType of experiment : in vivoType of animal : ratType of study : -N(Total) : -N(Treatment) : -Sex : -Age : -Route : Oral administrationDose/Conc.(herb) : 125 mg/kg/dayDuration : 18 hoursType of interaction : PharmacokineticsInteraction with drug : Enflurane*/Methylflurether/Efrane/EthraneDose/Conc.(drug) : -Result : NegativeRemark : Red ginseng extract was dissolved in 0.9% saline (0.5 ml) and administered with 22G gavage needle. rats were dosed 18 hours before administered enflurane 0.6 microliters/g i.p.Note : There were no statistically significant differences in hepatic microsomal cytochrome p-450 content or defluorination of enflurane and methoxyflurane between control and experimental groups using either red ginseng extract or powder.
