ABSTRACT
A study of the condition and function of a multienzymatic monoxygenase system in liver microsomes of rats bearing experimental Pliss' lymphosarcoma and Zajdela's ascites hepatoma showed synthesis and function of the key enzymes of the hydroxylating microsomes of the liver being inhibited and, consequently, drug metabolism slowed down.
Subject(s)
Liver Neoplasms, Experimental/enzymology , Lymphoma, Non-Hodgkin/enzymology , Microsomes, Liver/enzymology , Aminopyrine/pharmacokinetics , Aniline Compounds/pharmacokinetics , Aniline Hydroxylase/metabolism , Animals , Cytochrome P-450 Enzyme System/metabolism , Cytochrome b Group/metabolism , Cytochromes b5 , Enzyme Induction/drug effects , Hydroxylation , Male , Microsomes, Liver/drug effects , Neoplasm Transplantation , Phenobarbital/pharmacology , Rats , Time FactorsABSTRACT
Functions of pyridine nucleotide cofactors NADPH and NADH in N-demethylation of amidopyrine were studied under conditions of normal and malignant states. Contribution of NADH-specific transfer of electrons to microsomal N-demethylation was gradually augmented in the sequence: microsomes from liver tissue of rats with Zajdela hepatoma--microsomes of ascites hepatocytes. In this sequence both synergic effect of these cofactors and the rate of N-demethylcation, if NADH was used as a cofactor, were increased.