In vivo and in vitro effects of helenalin on mouse hepatic microsomal cytochrome P450

1991 ◽  
Vol 41 (2) ◽  
pp. 229-235 ◽  
Author(s):  
Dennis E. Chapman ◽  
David J. Holbrook ◽  
Stephen G. Chaney ◽  
Iris H. Hall ◽  
Lee Kuo-Hsiung
Keyword(s):  
Cytochrome P450 ◽  
Microsomal Cytochrome ◽  
Microsomal Cytochrome P450 ◽  
In Vitro Effects

scholarly journals Effect of 4-(4-Chlorobenzyl)pyridine on Rat Hepatic Microsomal Cytochrome P450 and Drug-Metabolizing Enzymes in Vivo and in Vitro.

2001 ◽  
Vol 24 (5) ◽  
pp. 505-509 ◽  
Author(s):  
Yasuna KOBAYASHI ◽  
Naomi OHSHIRO ◽  
Tadanori SASAKI ◽  
Shogo TOKUYAMA ◽  
Takashi TOBE ◽  
...  
Keyword(s):  
Cytochrome P450 ◽  
Drug Metabolizing Enzymes ◽  
Metabolizing Enzymes ◽  
Microsomal Cytochrome ◽  
Microsomal Cytochrome P450

In vitro biotransformation of atrazine by rat liver microsomal cytochrome P450 enzymes

1998 ◽  
Vol 116 (3) ◽  
pp. 181-198 ◽  
Author(s):  
Nobumitsu Hanioka ◽  
Hideto Jinno ◽  
Ken Kitazawa ◽  
Toshiko Tanaka-Kagawa ◽  
Tetsuji Nishimura ◽  
...  
Keyword(s):  
Cytochrome P450 ◽  
Rat Liver ◽  
Cytochrome P450 Enzymes ◽  
Microsomal Cytochrome ◽  
Microsomal Cytochrome P450

Inhibitory effects of H2-receptor antagonists on cytochrome P450 in male ICR mice

1995 ◽  
Vol 14 (8) ◽  
pp. 623-629 ◽  
Author(s):  
DH Kim ◽  
EJ Kim ◽  
SS Han ◽  
JK Roh ◽  
TC Jeong ◽  
...  
Keyword(s):  
Cytochrome P450 ◽  
Liver Microsomes ◽  
Receptor Antagonists ◽  
Sleeping Time ◽  
Icr Mice ◽  
In Vitro Effects ◽  
Hexobarbital Metabolism ◽  
Dose Dependent

1 The present study was undertaken to examine the effects of H2-receptor antagonists including newly developed mifentidine derivatives, IY-80843 and IY-80845, on cytochrome P450(P450) in vitro and in vivo. 2 Initially, 3-methylcholanthrene-, phenobarbital-, ethanol- and dexamethasone-induced liver microsomes were prepared from male ICR mice to study in vitro effects of above chemicals on ethoxyresorufin O- deethylase(EROD), pentoxyresorufin O-dealkylase(PROD), p-nitrophenol hydroxylase and erythromycin N-demethy lase(ERDM) activities, respectively. It was found that hist amine, cimetidine and famotidine were not inhibitory to four enzyme activities. Meanwhile, mifentidine slightly inhibited EROD and PROD activities and its derivatives IY-80843 and IY-80845 strongly inhibited PROD, EROD and ERDM activities. 3 Prolongation of hexobarbital-induced sleeping time was determined in male ICR mice to confirm in vitro inhibito ry effects of mifentidine and its derivatives in vivo. It was observed that cimetidine, mifentidine, IY-80843 and IY- 80845 caused dose-dependent increases in the sleeping time, indicating the inhibition of P450 responsible for hexobarbital metabolism. 4 It was concluded that mifentidine and its derivatives are P450 inhibitors and that our newly synthesized IY-80843 is most inhibitory. 5 The present results indicate that mifentidine and its derivatives not only antagonise the H 2-receptor but also inhibit P450 enzymes.

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