Evidence map›Paper›PMID 26839710›Full record

ReviewNeural plasticity2016

Lipidomic Analysis of Endocannabinoid Signaling: Targeted Metabolite Identification and Quantification.

Jantana Keereetaweep, Kent D Chapman

Open access · goldAbstract readReview
In one paragraph

Review in Neural plasticity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

8 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Enhanced seedling growth by 3-Plant direct · 2022
    Article
  5. Review
  6. Review
  7. Review
  8. Article
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

2 authors at 1 institution in 1 country.

Jantana KeereetaweepDepartment of Biological Sciences, Center for Plant Lipid Research, University of North Texas, Denton, TX 76203, USA; Brookhaven National Laboratory, 50 Bell Avenue, Building 463, P.O. Box 5000, Upton, NY 11973-5000, USA.
Kent D ChapmanDepartment of Biological Sciences, Center for Plant Lipid Research, University of North Texas, Denton, TX 76203, USA.
University of North Texas · US

Funding

UC Irvine Alzheimer's Disease Research Center Induced Pluripotent Stem Cell CoreP50AG016573 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI LAFERLA, FRANK M · 2000 to 2019
$37.0M
Characterization of Anandamide Transport in BrainR01DA012413 · NIDA · UNIVERSITY OF CALIFORNIA-IRVINE · PI PIOMELLI, DANIELE · 1998 to 2016
$4.7M
NOVEL BRAIN CANNABINOID LIGANDR01DA012447 · NIDA · UNIVERSITY OF CALIFORNIA-IRVINE · PI PIOMELLI, DANIELE · 1998 to 2010
$2.4M
Role of oleoylethanolamide in the control of food intakeR01DK073955 · NIDDK · UNIVERSITY OF CALIFORNIA-IRVINE · PI PIOMELLI, DANIELE · 2007 to 2010
$1.3M
Role of endocannabinoid signaling in stress-coping behaviorRL1AA017538 · NIAAA · UNIVERSITY OF CALIFORNIA-IRVINE · PI PIOMELLI, DANIELE · 2007 to 2011
$1.1M
Role of Endocannabinoids in the Behavioral Consequences of Social IsolationR21DA022702 · NIDA · UNIVERSITY OF CALIFORNIA-IRVINE · PI PIOMELLI, DANIELE · 2006 to 2008
$1.0M
NCRR NIH HHS RR274-297/3504008NCRR NIH HHS RR274-305/3505998NIAAA NIH HHS 1RL1AA017538NIA NIH HHS P50 AG16573NIDA NIH HHS R01 DA-012413NIDA NIH HHS R01DA-012447NIDA NIH HHS R21DA-022702NIDDK NIH HHS R01DK-073955
6 · The paper itself

Abstract

The endocannabinoids N-arachidonoylethanolamide (or anandamide, AEA) and 2-arachidonoylglycerol (2-AG) belong to the larger groups of N-acylethanolamines (NAEs) and monoacylglycerol (MAG) lipid classes, respectively. They are biologically active lipid molecules that activate G-protein-coupled cannabinoid receptors found in various organisms. After AEA and 2-AG were discovered in the 1990s, they have been extensively documented to have a broad range of physiological functions. Along with AEA, several NAEs, for example, N-palmitoylethanolamine (PEA), N-stearoylethanolamine (SEA), and N-oleoylethanolamine (OEA) are also present in tissues, usually at much larger concentrations than AEA. Any perturbation that involves the endocannabinoid pathway may subsequently alter basal level or metabolism of these lipid mediators. Further, the altered levels of these molecules often reflect pathological conditions associated with tissue damage. Robust and sensitive methodologies to analyze these lipid mediators are essential to understanding how they act as endocannabinoids. The recent advances in mass spectrometry allow researchers to develop lipidomics approaches and several methodologies have been proposed to quantify endocannabinoids in various biological systems.

Indexed as

AnimalsEndocannabinoidsMass SpectrometryReceptors, CannabinoidSignal TransductionEndocannabinoidsReceptors, Cannabinoid

Identifiers

PMID26839710
PMCPMC4709765
OpenAlexW2279911584

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.