In vivo and in vitro effects of deltamethrin on cytochrome p450 monooxygenase activity in carp (cyprinus carpio L.) liver

1997 ◽  
Vol 32 (5) ◽  
pp. 789-802 ◽  
Author(s):  
L. Banka ◽  
K. A. Deer ◽  
J. Nemcsok ◽  
M. Abraham
Keyword(s):  
Cytochrome P450 ◽  
Cyprinus Carpio ◽  
Cytochrome P450 Monooxygenase ◽  
P450 Monooxygenase ◽  
Monooxygenase Activity ◽  
Carp Cyprinus Carpio ◽  
In Vitro Effects

Cytochrome P450 Monooxygenase Activity in the Dark Southern Subterranean Termite (Isoptera: Rhinotermitidae)

1998 ◽  
Vol 91 (5) ◽  
pp. 1131-1135 ◽  
Author(s):  
Steven M. Valles ◽  
Weste L. A. Osbrink ◽  
Faith M. Oi ◽  
Richard J. Brenner ◽  
Janine E. Powell
Keyword(s):  
Cytochrome P450 ◽  
Cytochrome P450 Monooxygenase ◽  
Subterranean Termite ◽  
P450 Monooxygenase ◽  
Monooxygenase Activity

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.

scholarly journals Purification of Cytochrome P450 and Ferredoxin, Involved in Bisphenol A Degradation, from Sphingomonas sp. Strain AO1

2005 ◽  
Vol 71 (12) ◽  
pp. 8024-8030 ◽  
Author(s):  
Miho Sasaki ◽  
Ayako Akahira ◽  
Ko-ichi Oshiman ◽  
Tetsuaki Tsuchido ◽  
Yoshinobu Matsumura
Keyword(s):  
Mass Spectrometry ◽  
Cytochrome P450 ◽  
Bisphenol A ◽  
Cytochrome P450 Monooxygenase ◽  
Mass Spectrometry Analysis ◽  
Monooxygenase System ◽  
P450 Monooxygenase ◽  
Monooxygenase Activity ◽  
Chromatography Analysis ◽  
Ferredoxin Reductase

ABSTRACT In a previous study (M. Sasaki, J. Maki, K. Oshiman, Y. Matsumura, and T. Tsuchido, Biodegradation 16:449-459, 2005), the cytochrome P450 monooxygenase system was shown to be involved in bisphenol A (BPA) degradation by Sphingomonas sp. strain AO1. In the present investigation, we purified the components of this monooxygenase, cytochrome P450 (P450bisd), ferredoxin (Fdbisd), and ferredoxin reductase (Redbisd). We demonstrated that P450bisd and Fdbisd are homodimeric proteins with molecular masses of 102.3 and 19.1 kDa, respectively, by gel filtration chromatography analysis. Spectroscopic analysis of Fdbisd revealed the presence of a putidaredoxin-type [2Fe-2S] cluster. P450bisd, in the presence of Fdbisd, Redbisd, and NADH, was able to convert BPA. The Km and k cat values for BPA degradation were 85 ± 4.7 μM and 3.9 ± 0.04 min−1, respectively. NADPH, spinach ferredoxin, and spinach ferredoxin reductase resulted in weak monooxygenase activity. These results indicated that the electron transport system of P450bisd might exhibit strict specificity. Two BPA degradation products of the P450bisd system were detected by high-performance liquid chromatography analysis and were thought to be 1,2-bis(4-hydroxyphenyl)-2-propanol and 2,2-bis(4-hydroxyphenyl)-1-propanol based on mass spectrometry-mass spectrometry analysis. This is the first report demonstrating that the cytochrome P450 monooxygenase system in bacteria is involved in BPA degradation.

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