Literature DB >> 26529

Metabolism and tissue distribution of mono-2-ethylhexyl phthalate in the rat.

I Chu, D C Villeneuve, V Secours, C Franklin, G Rock, A Viau.   

Abstract

The absorption, distribution and metabolic excretion of mono-2-ethylhexyl [7-14C]phthalate (MEHP) were studied in the rat. This compound was readily absorbed from the gastrointestinal tract. Radioactivity following intravenous administration of 14C-MEHP was rapidly distributed in all tissues, with the highest levels occurring in the liver, kidney, and urinary bladder. Excretion of radioactivity was rapid and approximately 80% of the dose was eliminated 24 hr after oral administration, 72% in the urine and 8% in feces. MEHP was extensively metabolized after oral administration, and the major urinary metabolites were identified as an alcohol, a ketone, and an acid resulting from the side-chain oxidation of MEHP. A trace of o-phthalic acid was also identified.

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Year:  1978        PMID: 26529

Source DB:  PubMed          Journal:  Drug Metab Dispos        ISSN: 0090-9556            Impact factor:   3.922


  13 in total

1.  Urinary phthalate metabolites in relation to biomarkers of inflammation and oxidative stress: NHANES 1999-2006.

Authors:  Kelly K Ferguson; Rita Loch-Caruso; John D Meeker
Journal:  Environ Res       Date:  2011-02-23       Impact factor: 6.498

Review 2.  Adipose Tissue as a Site of Toxin Accumulation.

Authors:  Erin Jackson; Robin Shoemaker; Nika Larian; Lisa Cassis
Journal:  Compr Physiol       Date:  2017-09-12       Impact factor: 9.090

3.  An assessment of the teratogenicity in the rat and mutagenicity in Salmonella of mono-2-ethylhexyl phthalate.

Authors:  J A Ruddick; D C Villeneuve; I Chu; E Nestmann; D Miles
Journal:  Bull Environ Contam Toxicol       Date:  1981-08       Impact factor: 2.151

4.  Sub-acute and sub-chronic toxicity of mono-2-ethylhexyl phthalate in the rat.

Authors:  I Chu; V E Secours; I A Marino; D C Villeneuve; V E Valli
Journal:  Arch Environ Contam Toxicol       Date:  1981       Impact factor: 2.804

5.  Absorption, distribution and metabolism of epoxystearic acid in the rat.

Authors:  I Chu; D C Villeneuve; V Secours; A Viau
Journal:  Bull Environ Contam Toxicol       Date:  1979-07       Impact factor: 2.151

6.  Phthalate esters used as plasticizers in packed red blood cell storage bags may lead to progressive toxin exposure and the release of pro-inflammatory cytokines.

Authors:  Leonard T Rael; Raphael Bar-Or; Daniel R Ambruso; Charles W Mains; Denetta S Slone; Michael L Craun; David Bar-Or
Journal:  Oxid Med Cell Longev       Date:  2009 Jul-Aug       Impact factor: 6.543

7.  Disposition of orally administered di-(2-ethylhexyl) phthalate and mono-(2-ethylhexyl) phthalate in the rat.

Authors:  O A Teirlynck; F Belpaire
Journal:  Arch Toxicol       Date:  1985-09       Impact factor: 5.153

8.  Non-linearities in the pharmacokinetics of di-(2-ethylhexyl) phthalate and metabolites in male rats.

Authors:  P Sjöberg; U Bondesson; M Hammarlund
Journal:  Arch Toxicol       Date:  1985-12       Impact factor: 5.153

9.  Induction of propranolol metabolism in isolated rats hepatocytes treated by di(2-ethylhexyl) phthalate (DEHP) and mono(2-ethylhexyl) phthalate (MEHP).

Authors:  K Kambia; T Dine; B Gressier; B Benaji; M A Faouzi; T Dupin-Spriet; M Luyckx; C Brunet
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2003 Jul-Sep       Impact factor: 2.569

10.  Fetotoxic effects of mono-2-ethylhexyl phthalate (MEHP) in mice.

Authors:  I Tomita; Y Nakamura; Y Yagi; K Tutikawa
Journal:  Environ Health Perspect       Date:  1986-03       Impact factor: 9.031

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