Abstract
Cadmium chloride (CdCl2) pretreatment produced a marked decrease in the activity of the hepatic microsomal mono-oxygenase enzyme systems in male New Zealand white rabbits. Following in vivo sub-lethal doses (6 mg/kg i.p.) of CdCl2 for 5 days, significant decreases in the levels of cytochrome P-450 and in the microsomal metabolism of a range of substrates were observed. Pretreatment of rabbits with phenobarbitone significantly increased the levels of cytochrome P-450 and also increased the metabolism of all the substrates used. The inhibition pattern produced by CdCl2 remained the same in control and PB-pretreated rabbits. CdCl2 treatment did not result in any change in the levels of cytochrome b5 or cytochrome-c-reductase.
Original language | English (US) |
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Pages (from-to) | 45-49 |
Number of pages | 5 |
Journal | Pharmaceutical Science Communications |
Volume | 4 |
Issue number | 1 |
State | Published - 1993 |
Externally published | Yes |
Keywords
- Acetanilide-4-hydroxylase
- Aminopyrine-N-demethylase
- Aniline-4-hydroxylase
- Benzphetamine-N-demethylase,
- Cadmium chloride
- Cytochrome P-450
- Cytochrome b
- Cytochrome-c-reductase
- N-demethylases
- Phenobarbitone
- Pretreatment
- Rabbits
ASJC Scopus subject areas
- Molecular Medicine
- Pharmacology