Literature DB >> 6897933

Increased metabolic clearance of acetaminophen with oral contraceptive use.

D R Abernethy, M Divoll, H R Ochs, B Ameer, D J Greenblatt.   

Abstract

The effect of chronic low-dose oral contraceptive steroid use on the pharmacokinetics of intravenous acetaminophen was determined. Eight women using low-dose (under 50 micrograms) estrogen oral contraceptive steroid for more than 3 months were matched for age and weight (mean age, 25.9 years; mean weight, 58.3 kg) with 8 female controls not using the steroid (mean age, 26.0 years; mean weight, 55.5 kg). No subject was taking other drugs. Oral contraceptive steroid subjects had a lower elimination half-life of acetaminophen (2.12 hours) than controls (2.71 hours) (P less than .005). Volume of distribution was similar for both groups (oral contraceptive group, 1.04 liters/kg; controls, 0.96 liters/kg; NS). Total metabolic clearance was significantly higher in oral contraceptive subjects (5.81 ml/min/kg, versus 4.12 ml/min/kg for controls; P less than .02). As volume of distribution and body weight are similar for both groups, the decrease in acetaminophen elimination half-life among contraceptive steroid users is the result of increased total metabolic clearance. Thus, low-dose estrogen oral contraceptive steroid may stimulate the metabolism of a conjugatively metabolized drug such as acetaminophen, in contrast to contraceptive steroid impairment of the clearance of some oxidatively metabolized drugs, with antipyrine being the prototype.

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Year:  1982        PMID: 6897933

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  13 in total

1.  Acetaminophen pharmacokinetics in women receiving conjugated estrogen.

Authors:  J M Scavone; D J Greenblatt; G T Blyden; B G Luna; J S Harmatz
Journal:  Eur J Clin Pharmacol       Date:  1990       Impact factor: 2.953

2.  Single dose primaquine has no effect on paracetamol clearance.

Authors:  D J Back; J F Tjia
Journal:  Eur J Clin Pharmacol       Date:  1987       Impact factor: 2.953

3.  Lack of impairment of fluocortolone disposition in oral contraceptive users.

Authors:  U F Legler
Journal:  Eur J Clin Pharmacol       Date:  1988       Impact factor: 2.953

4.  Impairment of caffeine clearance by chronic use of low-dose oestrogen-containing oral contraceptives.

Authors:  D R Abernethy; E L Todd
Journal:  Eur J Clin Pharmacol       Date:  1985       Impact factor: 2.953

5.  Pharmacokinetics of Bupropion and Its Pharmacologically Active Metabolites in Pregnancy.

Authors:  Valentina M Fokina; Meixiang Xu; Erik Rytting; Sherif Z Abdel-Rahman; Holly West; Cheryl Oncken; Shannon M Clark; Mahmoud S Ahmed; Gary D V Hankins; Tatiana N Nanovskaya
Journal:  Drug Metab Dispos       Date:  2016-08-15       Impact factor: 3.922

6.  Regulation of UDP-glucuronosyltransferase (UGT) 1A1 by progesterone and its impact on labetalol elimination.

Authors:  H Jeong; S Choi; J W Song; H Chen; J H Fischer
Journal:  Xenobiotica       Date:  2008-01       Impact factor: 1.908

7.  Gender and oral contraceptive steroids as determinants of drug glucuronidation: effects on clofibric acid elimination.

Authors:  J O Miners; R A Robson; D J Birkett
Journal:  Br J Clin Pharmacol       Date:  1984-08       Impact factor: 4.335

Review 8.  Glucuronidation of drugs. A re-evaluation of the pharmacological significance of the conjugates and modulating factors.

Authors:  H K Kroemer; U Klotz
Journal:  Clin Pharmacokinet       Date:  1992-10       Impact factor: 6.447

9.  Salivary antipyrine half-life during injectable progestagen contraception.

Authors:  J V Joshi; K C Gupta; K T Hazari; J Gokral; S Pohujani; R Satoskar
Journal:  Clin Pharmacokinet       Date:  1986 Mar-Apr       Impact factor: 6.447

10.  Paracetamol pharmacokinetics during the first trimester of human pregnancy.

Authors:  L Beaulac-Baillargeon; S Rocheleau
Journal:  Eur J Clin Pharmacol       Date:  1994       Impact factor: 2.953

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