Racial differences in drug metabolizing ability: A study with antipyrine in the Sudan

The kinetic disposition of antipyrine following oral administration of 1,200 mg has been investigated in 11 normal Sudanese subjects living in Sudan, 9 Sudanese subjects living in England for al least 2 yr, and 19 normal English subjects living in England. Sudanese subjects living in Sudan had significantly lower mean antipyrine clearance and higher volume of distribution than the English group (−28% and +30%, respectively). There was no significant difference for antipyrine clearance between English and Sudanese subjects living in England, but the volume of distribution of antipyrine was higher (16%) in the Sudanese subjects. The mean half‐lives of the three groups difJered significantly. We conclude that differences in disposition of antipyrine between native English and Sudanese populations was predominantly due to environmental factors.

[1]  A. Conney,et al.  Nutrition and chemical biotransformations in man , 1977, Clinical pharmacology and therapeutics.

[2]  K. Krishnaswamy,et al.  Microsomal enzymes in malnutrition as determined by plasma half life of antipyrine. , 1977, British medical journal.

[3]  R. Branch,et al.  The relationship between liver volume, antipyrine clearance and indocyanine green clearance before and after phenobarbitone administration in man. , 1976, British journal of clinical pharmacology.

[4]  J. Mucklow,et al.  Factors affecting antipyrine metabolism in West African villagers , 1976, Clinical pharmacology and therapeutics.

[5]  A. H. Norris,et al.  Antipyrine metabolism in man: Influence of age, alcohol, caffeine, and smoking , 1975, Clinical pharmacology and therapeutics.

[6]  E. Vesell,et al.  Comparison of plasma levels of antipyrine, tolbutamide, and warfarin after oral and intravenous administration , 1974, Clinical pharmacology and therapeutics.

[7]  T. Campbell,et al.  Role of nutrition in the drug-metabolizing enzyme system. , 1974, Pharmacological reviews.

[8]  L. Ranek,et al.  Clearance of Antipyrine‐Dependence of Quantitative Liver Function , 1974, European journal of clinical investigation.

[9]  R. Branch,et al.  Determinants of serum antipyrine half-lives in patients with liver disease , 1973, Gut.

[10]  A. Conney,et al.  Decreased Concentration of Phenacetin in Plasma of Cigarette Smokers , 1972, Science.

[11]  S. Thorgeirsson,et al.  Drug interactions with warfarin: studies with dichloralphenazone, chloral hydrate and phenazone (antipyrine). , 1971, Clinical science.

[12]  E. Vesell,et al.  Genetic Control of Drug Levels in Man: Antipyrine , 1968, Science.

[13]  A. Conney,et al.  Cigarette Smoking: Stimulatory Effect on Metabolism of 3,4-Benzpyrene by Enzymes in Human Placenta , 1968, Science.

[14]  A. Conney Pharmacological implications of microsomal enzyme induction. , 1967, Pharmacological reviews.

[15]  B. Brodie,et al.  The estimation of antipyrine in biological materials. , 1949, The Journal of biological chemistry.