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PMID: 2198572 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Endogenous biosynthesis of arachidonic acid epoxides in humans: increased formation in pregnancy-induced hypertension.

Catella F, Lawson JA, Fitzgerald DJ, FitzGerald GA

Abstract

Arachidonic acid is metabolized by means of P450 isoenzyme(s) to form epoxyeicosatrienoic acids (EETs) and their corresponding dihydroxy derivatives (DHETs). In the present study, we established the presence in human urine of 8,9-, 11,12-, and 14,15-EETs and their corresponding DHETs by developing quantitative assays and using negative ion, chemical ionization GC/MS and octadeuterated internal standards. Urinary excretion of 8,9- and 11,12-DHET increased in healthy pregnant women compared with nonpregnant female volunteers. By contrast, excretion of 11,12-DHET and 14,15-DHET, but not the 8,9-DHET regioisomer, increased even further in patients with pregnancy-induced hypertension. Intravenous administration of [3H]14,15-EET to three dogs markedly increased its DHET in plasma. The terminal half-life ranged from 7.9-12.3 min and the volume of distribution (3.5-5.3 liters) suggested limited distribution outside the plasma compartment. Negligible radioactivity was detected in urine; this fact infers that under physiological circumstances, urinary DHETs largely derive from the kidney. That P450 metabolites of arachidonic acid are formed in humans supports the hypothesis that these metabolites contribute to the physiological response to normal pregnancy and the pathophysiology of pregnancy-induced hypertension.

MeSH Terms
8,11,14-Eicosatrienoic Acid/analogs & derivatives,pharmacokinetics,urine Animals Dogs Fatty Acids, Unsaturated/urine Female Gas Chromatography-Mass Spectrometry Humans Hypertension/metabolism,urine Pre-Eclampsia/metabolism Pregnancy Pregnancy Complications, Cardiovascular/metabolism Radioisotope Dilution Technique Reference Values Tritium
Chemicals
Fatty Acids, Unsaturated Tritium 11,12-epoxy-5,8,14-eicosatrienoic acid 8,9-epoxyeicosatrienoic acid 14,15-epoxy-5,8,11-eicosatrienoic acid 8,11,14-Eicosatrienoic Acid
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Catella F
Division of Clinical Pharmacology, Vanderbilt University, Nashville, TN 37232.
Lawson J A
Fitzgerald D J
FitzGerald G A
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37 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1990-08-00
Pages
5893-7
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC54435
Subset
IM
Grants
NICHD NIH HHS · HD 05797 · United States
NHLBI NIH HHS · HL 30400 · United States
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