Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Polycyclic hydrocarbons, hepatic microsomal enzymes inducers

The alteration of hemoprotein(s) P-450 subpopulations in the rat may be observed spectrally, because after treatment of rats with polycyclic aromatic hydrocarbons, the Soret maximum of the carbonmonoxyferrocytochrome complex undergoes a hypsochromic shift from 450 to 448nm (50). This blue shift was not seen with rainbow trout hepatic microsomes (29,30). However, this does not preclude the induction of novel hemoproteins P-450 since (a) the induced hemoprotein(s) maty not differ spectrally from the constitutive enzymes and (b) the induced-hemoprotein may account for only a small proportion of total hemoprotein P-450, and hence its contribution to the position of the Soret maximum of carbon monoxide-treated reduced microsomes may be negligible. The latter suggestion is supported by the work of Bend et al. with the little skate. These workers have shown that hepatic microsomes from 1, 2,3,4-dibenzanthracene treated skates did not exhibit a hypsochromic shift when compared to control microsomes, however, partially purified hemoprotein exhibited an absorbance maxima at 448 nm (51). [Pg.326]


See other pages where Polycyclic hydrocarbons, hepatic microsomal enzymes inducers is mentioned: [Pg.322]    [Pg.119]    [Pg.319]    [Pg.131]    [Pg.433]    [Pg.5]    [Pg.6]    [Pg.123]    [Pg.99]    [Pg.452]    [Pg.138]    [Pg.2180]   


SEARCH



Enzyme hepatic

Enzyme inducers

Enzyme microsomal

Enzymes, induced

Hepatic microsomal

Hepatic microsomal enzyme

Induced polycycle

Microsomal

Microsomal enzyme inducers

Microsomal microsomes

Microsome enzymes

Microsome hepatic

Microsomes

Polycyclic hydrocarbons, hepatic microsomal

© 2024 chempedia.info