Evidence map›Paper›PMID 24760994›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2014

Mercaptoacetate and fatty acids exert direct and antagonistic effects on nodose neurons via GPR40 fatty acid receptors.

Rebecca A Darling, Huan Zhao, Dallas Kinch, Ai-Jun Li, Steven M Simasko, Sue Ritter

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. The critical role of gut-brain signalling in eating behaviour and obesity.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  2. Mechanistic insights into the liver-brain axis during chronic liver disease.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  3. Review
  4. Review
  5. Hepatic interoception in health and disease.Autonomic neuroscience : basic & clinical · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. The vagus neurometabolic interface and clinical disease.International journal of obesity (2005) · 2018
    Review
  13. Review
  14. Article
  15. Review
  16. Bugs, guts and brains, and the regulation of food intake and body weight.International journal of obesity supplements · 2016
    Review
  17. Deletion of GPR40 fatty acid receptor gene in mice blocks mercaptoacetate-induced feeding.American journal of physiology. Regulatory, integrative and comparative physiology · 2016
    Article
  18. Mercaptoacetate blocks fatty acid-induced GLP-1 secretion in male rats by directly antagonizing GPR40 fatty acid receptors.American journal of physiology. Regulatory, integrative and comparative physiology · 2016
    Article
  19. Article
  20. Enhancing hepatic mitochondrial fatty acid oxidation stimulates eating in food-deprived mice.American journal of physiology. Regulatory, integrative and comparative physiology · 2015
    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

6 authors at 1 institution in 1 country.

Rebecca A DarlingProgram in Neuroscience, Washington State University, Pullman, Washington.
Huan ZhaoProgram in Neuroscience, Washington State University, Pullman, Washington.
Dallas KinchProgram in Neuroscience, Washington State University, Pullman, Washington.
Ai-Jun LiProgram in Neuroscience, Washington State University, Pullman, Washington.
Steven M SimaskoProgram in Neuroscience, Washington State University, Pullman, Washington.
Sue RitterProgram in Neuroscience, Washington State University, Pullman, Washington sjr@vetmed.wsu.edu.
Washington State University · US

Funding

NEURAL SUBSTRATES OF METABOLIC CONTROLS OF INGESTIONR01DK040498 · NIDDK · WASHINGTON STATE UNIVERSITY · PI RITTER, W. SUE · 1989 to 2014
$4.3M
Mechanisms of Fatty Acid Control of Feeding BehaviorR01DK097437 · NIDDK · WASHINGTON STATE UNIVERSITY · PI RITTER, W. SUE · 2013 to 2016
$1.3M
Mechanisms of activation of vagal afferent neuronsR01DK067146 · NIDDK · WASHINGTON STATE UNIVERSITY · PI SIMASKO, STEVEN M · 2005 to 2009
$1.3M
Hindbrain catecholamine neurons and body fatR01DK081546 · NIDDK · WASHINGTON STATE UNIVERSITY · PI RITTER, W. SUE · 2008 to 2011
$1.2M
NIDDK NIH HHS DK-040498NIDDK NIH HHS DK-067146NIDDK NIH HHS DK-081546NIDDK NIH HHS DK-097437NIDDK NIH HHS R01 DK040498NIDDK NIH HHS R01 DK097437
6 · The paper itself

Abstract

β-mercaptoacetate (MA) is a drug known to block mitochondrial oxidation of medium- and long-chain fatty acids (FAs) and to stimulate feeding. Because MA-induced feeding is vagally dependent, it has been assumed that the feeding response is mediated by MA's antimetabolic action at a peripheral, vagally innervated site. However, MA's site of action has not yet been identified. Therefore, we used fluorescent calcium measurements in isolated neurons from rat nodose ganglia to determine whether MA has direct effects on vagal sensory neurons. We found that MA alone did not alter cytosolic calcium concentrations in nodose neurons. However, MA (60 μM to 6 mM) significantly decreased calcium responses to both linoleic acid (LA; 10 μM) and caprylic acid (C8; 10 μM) in all neurons responsive to LA and C8. GW9508 (40 μM), an agonist of the FA receptor, G protein-coupled receptor 40 (GPR40), also increased calcium levels almost exclusively in FA-responsive neurons. MA significantly inhibited this response to GW9508. MA did not inhibit calcium responses to serotonin, high K(+), or capsaicin, which do not utilize GPRs, or to CCK, which acts on a different GPR. GPR40 was detected in nodose ganglia by RT-PCR. Results suggest that FAs directly activate vagal sensory neurons via GPR40 and that MA antagonizes this effect. Thus, we propose that MA's nonmetabolic actions on GPR40 membrane receptors, expressed by multiple peripheral tissues in addition to the vagus nerve, may contribute to or mediate MA-induced stimulation of feeding.

Indexed as

AnimalsCalciumCalcium SignalingCaprylatesCells, CulturedDose-Response Relationship, DrugEatingFatty AcidsLinoleic AcidMaleNodose GanglionRatsRats, Sprague-DawleyReceptors, G-Protein-CoupledSensory Receptor CellsThioglycolates2-mercaptoacetateCalciumCaprylatesFatty AcidsG-protein-coupled receptor 40, ratLinoleic Acidoctanoic acidReceptors, G-Protein-CoupledThioglycolatescalcium imagingfatty acidsG-protein coupled receptor 40nodose ganglionβ-mercaptoacetate

Identifiers

PMID24760994
PMCPMC4152161
OpenAlexW2089479938

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.