Literature DB >> 6528810

Metabolism of trimethoprim in neonatal and young pigs: comparative in vivo and in vitro studies.

N Gyrd-Hansen, C Friis, P Nielsen, F Rasmussen.   

Abstract

Metabolism of trimethoprim (TMP) was investigated in in vivo and in vitro experiments on 1 day (group A), 8 days (group B), and 60 days (group C) old piglets. In the in vivo studies piglets received an intravenous injection of 14C-trimethoprim. Urine was then collected for 3 hours after which the animals were killed. During the collection period 13, 24, and 40% of the dose was excreted in the urine in group A, B, and C, respectively. Trimethoprim and the following metabolites: Metabolite 1 and 4, minor metabolites, and conjugates were determined in plasma, liver, kidney, urine, and bile. The results show that newborn piglets have little capacity for oxidation of TMP while the ability to conjugate with glucuronic acid and sulfate seems somewhat higher. During the following 8 weeks a marked increase in the oxidative as well as conjugative potential took place. The microsomal fractions of liver and kidney were used for the in vitro metabolism studies of TMP. No metabolic activity could be demonstrated in the kidney preparations. Oxidative demethylation was just detectable in livers from the newborn piglets but increased considerably with age. Glucuronidation of metabolite 4 took place in the liver preparations from all three groups but at the highest rate in group C. The development in metabolic capacity was found to be qualitatively similar in vivo and in vitro.

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Year:  1984        PMID: 6528810     DOI: 10.1111/j.1600-0773.1984.tb02002.x

Source DB:  PubMed          Journal:  Acta Pharmacol Toxicol (Copenh)        ISSN: 0001-6683


  5 in total

1.  Distribution and elimination of 14C-ethion in laying hens and eggs after oral exposure.

Authors:  R D Mosha; N Gyrd-Hansen; P Nielsen
Journal:  Bull Environ Contam Toxicol       Date:  1990-09       Impact factor: 2.151

2.  Data Mining FAERS to Analyze Molecular Targets of Drugs Highly Associated with Stevens-Johnson Syndrome.

Authors:  Keith K Burkhart; Darrell Abernethy; David Jackson
Journal:  J Med Toxicol       Date:  2015-06

3.  Pharmacokinetics of sulfadimethoxine and sulfamethoxazole in combination with trimethoprim after oral single- and multiple-dose administration to healthy pigs.

Authors:  M J Mengelers; E R van Gogh; M B Huveneers; P E Hougee; H A Kuiper; A Pijpers; J H Verheijden; A S van Miert
Journal:  Vet Res Commun       Date:  2001-08       Impact factor: 2.459

4.  Metabolism and Disposition of Aditoprim in Swine, Broilers, Carp and Rats.

Authors:  Liye Wang; Lingli Huang; Yuanhu Pan; Kamil Kuča; Blanka Klímová; Qinghua Wu; Shuyu Xie; Ijaz Ahmad; Dongmei Chen; Yanfei Tao; Dan Wan; Zhenli Liu; Zonghui Yuan
Journal:  Sci Rep       Date:  2016-02-03       Impact factor: 4.379

5.  Metabolite Identification and Pharmacokinetic Behavior of Diaveridine in the Plasma of Pigs and Chickens Based on Radioactive Tracing Coupled With LC/MS-IT-TOF Assay.

Authors:  Liye Wang; Lihua Wen; Yuanhu Pan; Zhenzhen Wang; Kaixiang Zhou; Kun Mi; Zhenli Liu; Wei Qu; Lingli Huang
Journal:  Front Vet Sci       Date:  2022-01-18
  5 in total

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