Evidence map›Paper›PMID 30201384›Full record

ArticleChemistry and physics of lipids2018

A sensitive and improved throughput UPLC-MS/MS quantitation method of total cytochrome P450 mediated arachidonic acid metabolites that can separate regio-isomers and cis/trans-EETs from human plasma.

Maxwell Zeigler, Dale Whittington, Nona Sotoodehnia, Rozenn N Lemaitre, Rheem A Totah

Open access · bronzeAbstract read
In one paragraph

Article in Chemistry and physics of lipids, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Maxwell ZeiglerDepartment of Medicinal Chemistry, University of Washington, Box 357610, Seattle, WA 98195, USA. Electronic address: mzeigler@uw.edu.
Dale WhittingtonDepartment of Medicinal Chemistry, University of Washington, Box 357610, Seattle, WA 98195, USA. Electronic address: dalewhit@uw.edu.
Nona SotoodehniaCardiovascular Health Research Unit, Department of Medicine, University of Washington, 1730 Minor Ave, Suite 1360, Seattle, WA 98101, USA; Division of Cardiology, University of Washington, Box 356422, Seattle, WA 98195, USA. Electronic address: nsotoo@u.washington.edu.
Rozenn N LemaitreCardiovascular Health Research Unit, Department of Medicine, University of Washington, 1730 Minor Ave, Suite 1360, Seattle, WA 98101, USA. Electronic address: rozenl@uw.edu.
Rheem A TotahDepartment of Medicinal Chemistry, University of Washington, Box 357610, Seattle, WA 98195, USA. Electronic address: rtotah@uw.edu.
University of Washington · US

Funding

GENOMICS OF SUDDEN CARDIAC ARRESTR01HL088456 · NHLBI · UNIVERSITY OF WASHINGTON · PI SOTOODEHNIA, NONA · 2007 to 2011
$3.2M
CYP2J2 Mediated Eicosanoids in Arrhythmias and Sudden Cardiac ArrestR01HL128709 · NHLBI · UNIVERSITY OF WASHINGTON · PI SOTOODEHNIA, NONA, TOTAH, RHEEM ANGELA · 2015 to 2018
$2.9M
Epoxyeicosatrienoic acids, diabetes, and cardiovascular diseaseR01HL130880 · NHLBI · UNIVERSITY OF WASHINGTON · PI LEMAITRE, ROZENN, TOTAH, RHEEM ANGELA · 2016 to 2019
$2.8M
A Critical Role for Follistatin-like Protein-1 in Lung HomeostasisK08HL128809 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CAMPFIELD, BRIAN T · 2015 to 2019
$675k
NHLBI NIH HHS K08 HL128809NHLBI NIH HHS R01 HL088456NHLBI NIH HHS R01 HL128709NHLBI NIH HHS R01 HL130880
6 · The paper itself

Abstract

A method for the detection and quantification of hydroxyl and epoxy arachidonic acid (AA) metabolites in human plasma was developed using liquid-liquid extraction, phospholipid saponification followed by derivatization of the acid moiety and liquid chromatographic tandem mass spectrometric detection. Derivatization with a pyridinium analog allowed for detection in the positive ion mode, greatly improving sensitivity and the stability of the more labile AA metabolites. The entire method utilizes a 96-well plate format, increasing sample throughput, and was optimized to measure 5-, 8-, 9-, 11-, 12-, 15-, 19-, and 20- hydroxyeicosatetraenoic acid (HETE), 5,6-, 8,9-, 11,12-, and 14,15- dihydroxyeicosatrienoic acid (DHET), and the regio- and cis-/ trans- isomers of 5,6-, 8,9-, 11,12-, and 14,15-epoxyeicosatrienoic acid (EET). The method was validated for its applicability over the FA concentration range found in human plasma. Using 100 μL aliquots of pooled human plasma, EET levels, particularly 5,6-EET, were observed to be higher than previously reported, with measured concentrations of 23.6 ng/ml for 5,6-EET, 5.6 ng/mL for 5,6-trans-EET, 8.0 ng/mL for 8,9-EET, 1.9 ng/mL for 8,9-trans-EET, 8.8 ng/mL for 11,12-EET, 3.4 ng/mL for 11,12-trans-EET, 10.7 ng/mL for 14,15-EET, and 1.7 ng/mL 14,15-trans- EET. This method is suitable for large population studies to elucidate the complex interactions between the eicosanoids and various disease states and may be used for quantitation of a wide variety of fattyacids beyond eicosanoids from small volumes of human plasma.

Indexed as

8,11,14-Eicosatrienoic AcidArachidonic AcidChromatography, High Pressure LiquidCytochrome P-450 Enzyme SystemHumansMolecular StructureSolid Phase ExtractionStereoisomerismTandem Mass Spectrometry14,15-epoxy-5,8,11-eicosatrienoic acid8,11,14-Eicosatrienoic AcidArachidonic AcidCytochrome P-450 Enzyme SystemArachidonic acidDihydroxyeicosatrienoic acidEicosanoidsEpoxyeicosatrienoic acidHydroxyeicosatetraenoic acidLiquid chromatography tandem mass spectrometry

Identifiers

PMID30201384
PMCPMC6269592
OpenAlexW2891294889

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.