CANNABACEAE Cannabis sativa  L.

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 Thai / English name

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[1-1] of 1 article(s) found

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[1] CANNABIDIOL INDUCES EXPRESSION OF HUMAN CYTOCHROME P450 1A1 THAT IS POSSIBLY MEDIATED THROUGH ARYL HYDROCARBON RECEPTOR SIGNALING IN HEPG2 CELLS.
SATOSHI YAMAORI,YUKA KINUGASA,RONGRONG JIANG,ET AL.
LIFE SCI 2015 Vol.136(),87-93  $58405 [Full]

Part Used : ไม่ระบุ
Activity : CYP1A1 INDUCTION
Solvent/Active Compound : delta-9-tetrahydrocannabinol (delta9-THC)
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : -
Duration : -
Type of interaction : Pharmacodynamics
Interaction with drug : -
Dose/Conc.(drug) : -
Result : Positive
Remark : Delta-9 tetrahydrocannibinol (delta9-THC) and cannabidiol (CBD) increased the expression of CYP1A1 mRNA in a concentration-dependent manner; CYP1A1 mRNA level at 50 micromolar delta9-THC and CBD were 1.7- and 4.8- fold higher, respectively than control level. CBN had a less marked effect on CYP1A1 expression.
Note : Investigated the inducibility of cytochrome P450 1A1 (CYP1A1) by delta-9-tetrahydrocannabinol (delta9-THC) cannabidiol (CBD), and cannabinol (CBN), three major phytocannabinoids, using human hepatoma HepG2 cells. The expression of CYP1A1 and the aryl hydrocarbon receptor (AhR) was measured by a quantitative real-time polymerase chain reaction and/or Western blotting.

Part Used : ไม่ระบุ
Activity : CYP1A1 INDUCTION
Solvent/Active Compound : cannabidiol (CBD)
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : 0-50 micromolar
Duration : -
Type of interaction : Pharmacodynamics
Interaction with drug : -
Dose/Conc.(drug) : -
Result : Positive
Remark :
Note : Investigated the inducibility of cytochrome P450 1A1 (CYP1A1) by delta-9-tetrahydrocannabinol (delta9-THC) cannabidiol (CBD), and cannabinol (CBN), three major phytocannabinoids, using human hepatoma HepG2 cells. The expression of CYP1A1 and the aryl hydrocarbon receptor (AhR) was measured by a quantitative real-time polymerase chain reaction and/or Western blotting.

Part Used : ไม่ระบุ
Activity : CYP1A1 INDUCTION
Solvent/Active Compound : cannabidiol (CBN)
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : 0-50 micromolar
Duration : -
Type of interaction : Pharmacodynamics
Interaction with drug : -
Dose/Conc.(drug) : -
Result : Equivocal
Remark :
Note : Investigated the inducibility of cytochrome P450 1A1 (CYP1A1) by delta-9-tetrahydrocannabinol (delta9-THC) cannabidiol (CBD), and cannabinol (CBN), three major phytocannabinoids, using human hepatoma HepG2 cells. The expression of CYP1A1 and the aryl hydrocarbon receptor (AhR) was measured by a quantitative real-time polymerase chain reaction and/or Western blotting.


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