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PMID: 11447235 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Metabolism of prostaglandin glycerol esters and prostaglandin ethanolamides in vitro and in vivo.

The Journal of biological chemistry ·Vol. 276 ·No. 40 ·2001-10-05 ·Pages 36993-8

Kozak KR, Crews BC, Ray JL, Tai HH, Morrow JD, Marnett LJ

Abstract

Prostaglandin glycerol esters (PG-Gs) and prostaglandin ethanolamides (PG-EAs) are generated by the action of cyclooxygenase-2 on the endocannabinoids 2-arachidonylglycerol (2-AG) and arachidonylethanolamide, respectively. These novel eicosanoids may have unique pharmacological properties and/or serve as latent sources of prostaglandins at sites remote from their tissue of origin. Therefore, we investigated the metabolism of PG-Gs and PG-EAs in vitro and in vivo. PGE(2)-G was rapidly hydrolyzed in rat plasma to generate PGE(2) (t(1/2) = 14 s) but was only slowly metabolized in human plasma (t(1/2) > 10 min). An intermediate extent of metabolism of PGE(2)-G was observed in human whole blood (t(1/2) approximately 7 min). The parent arachidonylglycerol, 2-AG, and the more stable regioisomer, 1-AG, also were much more rapidly metabolized in rat plasma compared with human plasma. PGE(2)-EA was not significantly hydrolyzed in plasma, undergoing slow dehydration/isomerization to PGB(2)-EA. Both PGE(2)-G and PGE(2)-EA were stable in canine, bovine, and human cerebrospinal fluid. Human 15-hydroxyprostaglandin dehydrogenase, the enzyme responsible for the initial step in PG inactivation in vivo, oxidized both PGE(2)-G and PGE(2)-EA less efficiently than the free acid. The sterically hindered glyceryl prostaglandin was the poorest substrate examined in the E series. Minimal 15-hydroxyprostaglandin dehydrogenase oxidation of PGF(2 alpha)-G was observed. PGE(2)-G and PGE(2)-EA pharmacokinetics were assessed in rats. PGE(2)-G was not detected in plasma 5 min following an intravenous dose of 2 mg/kg. However, PGE(2)-EA was detectable up to 2 h following an identical dose, displaying a large apparent volume of distribution and a half-life of over 6 min. The results suggest that endocannabinoid-derived PG-like compounds may be sufficiently stable in humans to exert actions systemically. Furthermore, these results suggest that the rat is not an adequate model for investigating the biological activities of 2-arachidonylglycerol or glyceryl prostaglandins in humans.

MeSH Terms
Animals Cannabinoid Receptor Modulators Dinoprostone/analogs & derivatives,metabolism,pharmacokinetics Drug Stability Esters/metabolism Ethanolamines/metabolism,pharmacokinetics Glycerides/metabolism,pharmacokinetics Humans Hydroxyprostaglandin Dehydrogenases/metabolism Male Plasma/metabolism Prostaglandins/metabolism Rats Rats, Sprague-Dawley
Chemicals
Cannabinoid Receptor Modulators Esters Ethanolamines Glycerides Prostaglandins prostaglandin E2 glyceryl ester Hydroxyprostaglandin Dehydrogenases 15-hydroxyprostaglandin dehydrogenase Dinoprostone
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kozak K R
Department of Biochemistry and Chemistry, Vanderbilt-Ingram Cancer Center and Center in Molecular Toxicology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.
Crews B C
Ray J L
Tai H H
Morrow J D
Marnett L J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2001-10-05
Epub
2001-00-10
Pages
36993-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · CA77839 · United States
NIDDK NIH HHS · DK48831 · United States
NIGMS NIH HHS · GM15431 · United States
NHLBI NIH HHS · HL46296 · United States
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