๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Interaction of benzanthrone with cytochrome p450: Altered patterns of hepatic xenobiotic metabolism in rats

โœ Scribed by Das, Mukul ;Garg, Kalpana ;Joshi, Anjulika ;Singh, Giriraj B. ;Khanna, Subhash K.


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
783 KB
Volume
6
Category
Article
ISSN
0887-2082

No coin nor oath required. For personal study only.

โœฆ Synopsis


23%-34%), although the other enzyme, quinone reductase, which helps in the removal of toxic quinones, was found to be elevated (184%-199%). These results suggest several mechanisms by which benzanthrone may inhibit P450. This impairment of xenobiotic metabolism as well as the enhancement of lipid peroxidation may be relevant to the observed symptoms of benzanthrone-induced hepatotoxicity.


๐Ÿ“œ SIMILAR VOLUMES


Peroxidase, an alternate pathway to cyto
โœ Strohm, Bradford H. ;Kulkarni, Arun P. ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 830 KB

Peroxidase activity was partially purified from neonatal (3 to 6 days old) rat skin. The membrane-bound peroxidase activity was extracted with 0.5 M calcium chloride and was monitored spectrophotometrically at 470 nm with 2-methoxyphenol (guaiacol) and hydrogen peroxide as substrates. Subcellular di

Comparative study on altered hepatic met
โœ Jun-ichi Kusaba; Noriko Kajikawa; Hiromu Kawasaki; Yuji Kurosaki; Tetsuya Aiba ๐Ÿ“‚ Article ๐Ÿ“… 2012 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 147 KB ๐Ÿ‘ 2 views

To examine the mechanism accounting for the diverse alteration of hepatic metabolism of CYP3A substrates observed with renal function being severely impaired, the hepatic drug metabolizing activity was evaluated using liver microsomes prepared from rats with glycerol-induced acute renal failure (ARF

A simplified approach for evaluation of
โœ Dr Einosuke Tanaka; Akio Ishikawa; Yuji Yamamoto; Eiji Uchida; Shinichi Kobayash ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 402 KB ๐Ÿ‘ 2 views

## Abstract We determined the blood concentrations of caffeine (CA) and its three primary dimethylxanthine metabolites: theobromine (TB), paraxanthine (PX), and theophylline (TP), and trimethadione (TMO) and its demethylated metabolite dimethadione (DMO) after the simultaneous administration of CA