Determination of the half-life of antipyran in the plasma of Guatemalan individuals and its relationship with various factors including nutritional status

Authors

  • Reyna Julieta Roca Faculty of Chemical Sciences and Pharmacy
  • Beatriz Batres de Jiménez Faculty of Chemical Sciences and Pharmacy
  • José Héctor Aguilar Faculty of Chemical Sciences and Pharmacy

DOI:

https://doi.org/10.54495/Rev.Cientifica.v2i2.469

Keywords:

determination, half-life, antipyran, plasma, Guatemalan individuals, nutritional status

Abstract

The effect of malnutrition, age, sex, race, region, and body weight on the oxidative system responsible for the metabolism of many drugs, located in the hepatic macrosomes, was studied in a group of Guatemalan individuals. The plasma half-life of antipyrine, a substance metabolized by this system, was used as a parameter for this metabolism. To study the effect of these factors, two groups were used: the first consisting of 30 individuals (21 females and 9 males), ranging in age from 16 to 34 years and with adequate nutritional status; and the second group consisting of 27 individuals (13 females and 14 males), ranging in age from 16 to 35 years and with poor nutritional status. This last group was made up of individuals from various regions of the country. The group of individuals with adequate nutritional status showed lower values ​​for antipyrine half-life, with an average of 12.2 hours (s = 2.38), while the group of malnourished individuals had an average of 20.8 hours (s = 2.38), which is 70.4 times greater than the first group. The difference between the averages was statistically significant (p > 0.05), so it can be concluded that malnutrition increases the half-life of antipyrine in plasma and consequently decreases the capacity of the hepatic microsomal oxidative system, responsible for the metabolism of many drugs, which will probably affect any other drug that is metabolized in a similar way to antipyrine. Age, sex, and body weight did not affect the half-life of antipyrine in either of the two groups studied. Race and region also did not affect this time in the malnourished group. In all cases the differences obtained were not statistically significant (p<0.5s).

Downloads

Download data is not yet available.

References

Litter M. Farmacología Experimental y Clínica. 6 ed. Buenos Aires: El Ateneo, 1980. XIII +- 1953 p. (p.81-117).

Lu A. Liver Microsomal drug-metabolism enzyme System: functional components and their properties. Fed, Proc. 1976; 35: 2460-2463.

Davies D, Thorgeirsson SS. Mechanism of hepatic drug oxidation and its relationship to individual differences in rates of oxidation in man. Ann N Y Acad Sci 1971; 179:411-420. https://doi.org/10.1111/j.1749-6632.1971.tb46918.x

Fouts J, Adamson RH. Drug Metabolism in the newbom rabbitt. Science, 1959; 129:897-898. https://doi.org/10.1126/science.129.3353.897

Fraser H. Factors affecting antipyrine metabolism in West African villages. Clin Pharmacol Ther 1977; 22:799-808. https://doi.org/10.1002/cpt1977225part2799

Hart P, Farrell GG. Enhanced ' Drug metabolism in cigarrette smokers. Brit Med J 1978; 2:147-149. https://doi.org/10.1136/bmj.2.1907.147

Krishnaswamy K, Naidu AN. Microsomal enzymes in malnutrition as determined by plasma half-life of anti­pyrine. Brit Med J 1977; 1:538-540. https://doi.org/10.1136/bmj.1.6060.538

Miller ON. Nutrition and drug metabolism. Introduction. Fed. Proc 1976; 35:2459.

Wade A, Norred W. Effect of dietary lipid on drug metabolism enzymes. Fed Proc 1976; 35:2475-2479.

Campbell C, Hayes JR. The effect of quantity and quality dietary protein on drug metabolism. Fed Proc 1976; 35:2470-2474.

Melander A. Influence of food on the bioavailability of drugs. Clin Pharmacol 1978; 3:337-351. https://doi.org/10.2165/00003088-197803050-00001

Miranda CL, Webb RE. Effect of dietary protein on hepatic microsomal enzymes. J Nutr 1973; 103:1425. https://doi.org/10.1093/jn/103.10.1425

Zannoni V, Sato PH. Effect of certain vitamin deficiences on hepatic drug metabolism. Fed Proc 1976; 35:2464-2469.

Miller JL. Antipryrine plasma half-life: In-vivo indicator of oxidative metabolic capability in rhesus monkey. Pharmacology 1978; 16:279-286. https://doi.org/10.1159/000136780

Saenger P, Rifkind A, New M. Changes in drug metabolism in children with thyroid disorders. J Clin Endrocrinol Metab 1976; 42:155. https://doi.org/10.1210/jcem-42-1-155

Greenblatt D. Impairment of antipyrine clearance in humans by propranolol. Circulation 1978; 57:1161-1164. https://doi.org/10.1161/01.CIR.57.6.1161

Pirttiaho HI. Liver size and indices of drug metabolism in alcoholics. Eur J Clin Pharmacol 1978; 13:61-68. https://doi.org/10.1007/BF00606684

Eichelbaun MG. Influence of thyroid status on plasma half-life of antipyrine in man. N Engl J Med 1974; 290:1040. https://doi.org/10.1056/NEJM197405092901902

Ambre J. Antipyrine metabolism and bronchogenic carcinoma. J Med 1977;8:57-70.

Tschanz C. Metabolic disposition of antipyrine in patients with lung cáncer. Cáncer Res 1977; 37: 3881-3886.

Narang R, Mehta S, Mathur V. Pharmacokinetic study of antipyrine in malnourished children. Am J Clin Nutr 1977; 30: 1979-1982. https://doi.org/10.1093/ajcn/30.12.1979

Obel OK, Vere DW. Antipyrine and propranolol disposition in malnutrition. E Afr J Med 1978; 55:1-5.

Brodie B, Axelrod J, Soberman R, Levy B. The estimation of antipyrine in biological materials. J Biol Chem 1949;25:25-29.

Published

1984-12-31

How to Cite

Roca, R. J., Batres de Jiménez, B., & Héctor Aguilar, J. (1984). Determination of the half-life of antipyran in the plasma of Guatemalan individuals and its relationship with various factors including nutritional status. Revista Científica, 2(2), 7–12. https://doi.org/10.54495/Rev.Cientifica.v2i2.469

Issue

Section

Original Research Papers

Similar Articles

1 2 3 4 5 6 7 8 9 10 > >> 

You may also start an advanced similarity search for this article.