Stimulatory effects of chlordiazepoxide, diazepam and oxazepam on the drug-metabolizing enzymes in microsomes

J, Jabłońska; Knobloch, Krystyna; Majka, Jerzy; Wiśniewska-Knypl, Justyna M.

doi:10.1016/0300-483x(75)90075-x

“…Accordingly, changes in drug metabolism, because of liver disease or following the induction of the microsomal enzyme system, can alter the elimination of diazepam. In experiments in animals it was found that diazepam given in daily doses of 400 mg/kg bodyweight to rats stimulated hepatic microsomal metabolism as evidenced by acceleration of both p-hydroxylation of aniline and hydroxylation of benzene (Jablonska, Knobloch, Majka & Wisniewska-Knypl, 1975). In addition, rats, mice and guinea pigs treated with phenobarbitone showed an increase in diazepam metabolism affecting the different metabolites known in the degradation of diazepam elimination (Marucci, Fanelli, Mussini & Garattini, 1970 0306-5251/79/110557-07 $01.00 patients on long term diazepam therapy (Sellman, Kanto, Raijolo & Pekkarinen, 1975).…”

Section: Introductionmentioning

confidence: 99%

The effect of enzyme induction on diazepam metabolism in man.

Ohnhaus¹,

Park²,

Colombo³

et al. 1979

Brit J Clinical Pharma

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1 The elimination and metabolism of diazepam in man was investigated following the induction of the liver microsomal enzyme system by antipyrine. 2 Seven healthy volunteers were given 1200 mg antipyrine as an inducing agent for a period of 14 days. Before and after the induction period the elimination of diazepam and desmethyldiazepam was measured in the plasma by gaschromatography. As parameters of liver microsomal enzyme activity, antipyrine elimination and gamma‐glutamyl‐ transpeptidase in the plasma, D‐glucaric acid and 6‐beta‐ hydroxycortisol urinary excretion were measured on both occasions. 3 Following the induction period most parameters of microsomal enzyme activity measured were significantly changed indicating an increase of the microsomal enzyme system. The elimination of diazepam was significantly altered having a half‐life of 37 h before and 18 h afterwards combined with a significant increase in total body clearance after the induction period, although the volume of distribution remained unaltered. The formation of the main metabolite N‐ desmethyldiazepam was not changed, but its elimination was increased having a half‐life of 139 or 58 h respectively. 4 The elimination of unchanged diazepam and desmethyldiazepam is significantly increased by the induction of the liver microsomal enzyme system using antipyrine as an inducing agent in healthy volunteers, which might be important under certain clinical conditions.

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“…Accordingly, changes in drug metabolism, because of liver disease or following the induction of the microsomal enzyme system, can alter the elimination of diazepam. In experiments in animals it was found that diazepam given in daily doses of 400 mg/kg bodyweight to rats stimulated hepatic microsomal metabolism as evidenced by acceleration of both p-hydroxylation of aniline and hydroxylation of benzene (Jablonska, Knobloch, Majka & Wisniewska-Knypl, 1975). In addition, rats, mice and guinea pigs treated with phenobarbitone showed an increase in diazepam metabolism affecting the different metabolites known in the degradation of diazepam elimination (Marucci, Fanelli, Mussini & Garattini, 1970).…”

Section: Introductionmentioning

confidence: 99%