Kinetics of hepatic cytochrome P-450 reduction: correlation with spin state of the ferric heme
- 16 March 1982
- journal article
- research article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 21 (6) , 1324-1330
- https://doi.org/10.1021/bi00535a034
Abstract
The reduction kinetics of [rat] cytochrome P-450 are known to be biphasic, with a rapid initial phase and a slower subsequent phase, both of which appear linear in semilogarithmic plots. These biphasic reduction kinetics can be described in terms of a preequilibrium between high- and low-spin ferric states. Computer simulations are used which express the rate and extent of the fast phase or burst as being due to the initial proportion of high-spin cytochrome P-450. According to this simplified sequential model, the slow phase of reduction is controlled by the rate of formation of high-spin cytochrome P-450. The substrate-induced alterations in the reduction kinetics are likewise consistent with the model, which indicates that type I compounds exert their effect by virtue of a decrease in the rate constant controlling the shift from high-spin to low-spin ferric cytochrome. The model is further supported by the influence of temperature on the spin equilibrium and reduction kinetics. Potential influences of other intermediate steps in the reduction and assumptions in the hypothesis are described.This publication has 20 references indexed in Scilit:
- Temperature dependence of cytochrome P-450 reduction. A model for NADPH-cytochrome P-450 reductase:cytochrome P-450 interaction.Published by Elsevier ,2021
- Studies on the microsomal mixed function oxidase system: redox properties of detergent-solubilized NADPH-cytochrome P-450 reductaseBiochemistry, 1978
- Magnetic circular dichroism of purified forms of rabbit liver cytochromes P-450 and P-420Biochemistry, 1978
- Influences of substrates of different microsomal electron transfer pathways on the oxidation-reduction kinetics of microsomal cytochrome b5Archives of Biochemistry and Biophysics, 1978
- Temperature-dependent and -induced spectral characteristics and transitions of liver microsomesBiochemical and Biophysical Research Communications, 1977
- Evidence that puriified liver microsomal cytochrome P-450 is a one-electron acceptor.Journal of Biological Chemistry, 1977
- Studies on three microsomal electron transfer enzyme systemsArchives of Biochemistry and Biophysics, 1977
- Properties of electrophoretically homogeneous phenobarbital-inducible and beta-naphthoflavone-inducible forms of liver microsomal cytochrome P-450Journal of Biological Chemistry, 1976
- Coupling of spin, substrate, and redox equilibriums in cytochrome P450Biochemistry, 1976
- SPECTRAL STUDIES OF DRUG INTERACTION WITH HEPATIC MICROSOMAL CYTOCHROME1967