Evidence map›Paper›PMID 21415123›Full record

ArticleJournal of lipid research2011

The use of stable-isotopically labeled oleic acid to interrogate lipid assembly in vivo: assessing pharmacological effects in preclinical species.

David G McLaren, Timothy He, Sheng-Ping Wang, Vivienne Mendoza, Raymond Rosa, Karen Gagen, Gowri Bhat, Kithsiri Herath, Paul L Miller, Sloan Stribling and 14 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  8. DGAT1 mutation is linked to a congenital diarrheal disorder.The Journal of clinical investigation · 2012
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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

24 authors at 1 institution in 1 country.

David G McLarenMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ. Electronic address: David_McLaren@merck.com.
Timothy HeMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Sheng-Ping WangMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Vivienne MendozaMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Raymond RosaMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Karen GagenMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Gowri BhatMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Kithsiri HerathMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Paul L MillerMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Sloan StriblingMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Andrew TaggartMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Jason ImbriglioMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Jinqi LiuMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Dunlu ChenMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Shirly PintoMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
James M BalkovecMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Robert J DeVitaMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Donald J MarshMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Jose M Castro-PerezMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Alison StrackMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Douglas G JohnsMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Stephen F PrevisMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Brian K HubbardMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Thomas P RoddyMerck Research Laboratories, Merck & Co., Inc. Rahway, NJ.
Merck & Co., Inc., Rahway, NJ, USA (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of stable isotopically labeled substrates and analysis by mass spectrometry have provided substantial insight into rates of synthesis, disposition, and utilization of lipids in vivo. The information to be gained from such studies is of particular benefit to therapeutic research where the underlying causes of disease may be related to the production and utilization of lipids. When studying biology through the use of isotope tracers, care must be exercised in interpreting the data to ensure that any response observed can truly be interpreted as biological and not as an artifact of the experimental design or a dilutional effect on the isotope. We studied the effects of dosing route and tracer concentration on the mass isotopomer distribution profile as well as the action of selective inhibitors of microsomal tri-glyceride transfer protein (MTP) in mice and diacylglycerol acyltransferase 1 (DGAT1) in nonhuman primates, using a stable-isotopically labeled approach. Subjects were treated with inhibitor and subsequently given a dose of uniformly ¹³C-labeled oleic acid. Samples were analyzed using a rapid LC-MS technique, allowing the effects of the intervention on the assembly and disposition of triglycerides, cholesteryl esters, and phospholipids to be determined in a single 3 min run from just 10 μl of plasma.

Indexed as

Lipid MetabolismOleic AcidAnimalsCarrier ProteinsChlorocebus aethiopsCholesterol EstersChromatography, LiquidDiacylglycerol O-AcyltransferaseDrug Administration RoutesDrug Evaluation, PreclinicalEnzyme InhibitorsFemaleIsotope LabelingIsotopesLipoproteinsMaleCarrier ProteinsCholesterol EstersDiacylglycerol O-AcyltransferaseEnzyme InhibitorsIsotopesLipoproteinsmicrosomal triglyceride transfer proteinOleic AcidTriglycerides

Identifiers

PMID21415123
PMCPMC3090236
OpenAlexW2113743338

What OpenQuestion holds

Textmetadata
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.