Publication | Open Access
HEPATIC DRUG METABOLISM AND HAEM BIOSYNTHESIS IN LEAD‐POISONED RATS
43
Citations
26
References
1978
Year
Lipid PeroxidationHaem BiosynthesisRedox BiologyOxidative StressToxicologyHepatotoxicityDrug ToxicityHealth SciencesLead PretreatmentBiochemistryLiver PhysiologyCytochrome P-450MetabolomicsExperimental ToxicologyPharmacologyDrug-induced Liver InjuryPhysiologyMetabolismMedicine
1 Pretreatment of rats with intraperitoneal injections of lead was shown to result in a depression of the microsomal mixed function oxidase system, as assessed by a decrease in hepatic microsomal P-450 and b5 content and by a decrease in the activity of the enzymes aniline hydroxylase and aminopyrine demethylase. Lead had a more marked effect on cytochrome P-450 than b5. 2 The activity of the rate-limiting enzyme of haem biosynthesis, delta-aminolaevulinic acid synthase, was inversely correlated with the microsomal cytochrome P-450 content. 3 The activity of the haem biosynthetic enzymes delta-aminolaevulinic acid dehydratase, coproporphyrinogen oxidase and ferrochelatase were decreased by increasing lead pretreatment. 4 The activity of the haem catabolic enzyme, haem oxygenase, was increased by lead pretreatment.
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