Evidence map›Paper›PMID 19851310›Full record

ArticleObesity (Silver Spring, Md.)2010

Hypothalamic paraventricular nucleus lesion involvement in the sympathetic control of lipid mobilization.

Michelle T Foster, C Kay Song, Timothy J Bartness

Open access · bronzeAbstract read
In one paragraph

Article in Obesity (Silver Spring, Md.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.2field-weighted citation impact, top 28% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. A Review onEndocrine, metabolic & immune disorders drug targets · 2025
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  3. Article
  4. Review
  5. Modulation of the thermosensory system by oxytocin.Frontiers in molecular neuroscience · 2022
    Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Deletion of p22JCI insight · 2017
    Article
  12. Review
  13. Review
  14. Dnmt3a in Sim1 neurons is necessary for normal energy homeostasis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  15. Review
  16. Short and long sympathetic-sensory feedback loops in white fat.American journal of physiology. Regulatory, integrative and comparative physiology · 2014
    Article
  17. Molecular mechanisms of appetite regulation.Diabetes & metabolism journal · 2012
    Article
  18. Article
  19. Review
  20. 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

3 authors at 1 institution in 1 country.

Michelle T FosterDepartment of Biology and Center for Behavioral Neuroscience, Georgia State University, Atlanta, Georgia, USA.
C Kay Song
Timothy J Bartness
Georgia State University · US

Funding

Photoperiodic Control of ObesityR37DK035254 · NIDDK · GEORGIA STATE UNIVERSITY · PI BARTNESS, TIMOTHY JON · 2009 to 2014
$2.9M
NIDDK NIH HHS R37 DK035254NIDDK NIH HHS R37 DK35254
6 · The paper itself

Abstract

The sympathetic nervous system (SNS) innervation of white adipose tissue (WAT) is the principal initiator of lipolysis. Using pseudorabies virus, a transneuronal viral tract tracer, brain sites involved in the SNS outflow to WAT have been identified previously by us. One of these sites, the hypothalamic paraventricular nucleus (PVH) that shows predominantly unilateral sympathetic outflow from each half of the nucleus to ipsilaterally located WAT depots, was tested for laterality in lipid accumulation/mobilization in Siberian hamsters. First we tested whether unilateral PVH electrolytic lesions (PVHx) would increase lipid accumulation in WAT pads ipsilateral to the side of the PVHx. PVHx significantly increased body and WAT pad masses compared with sham PVHx; however, there was no laterality effect. In addition, bilateral PVHx increased body and WAT pad masses, as well as food intake, to a greater extent than did unilateral PVHx. We next tested for possible laterality effects on WAT lipid mobilization using food deprivation as the lipolytic stimulus in hamsters bearing unilateral or bilateral PVHx. Lipid mobilization was not prevented, as indicated indirectly by WAT mass and thus laterality of lipid mobilization could not be tested. We then tested whether removal of adrenal catecholamines via adrenal demedullation (ADMEDx) alone, or combined with bilateral PVHx, would block food deprivation-induced lipid mobilization, but neither did so. These results suggest that an intact PVH is not necessary for food deprivation-induced lipid mobilization and support the primacy of the SNS innervation of WAT, rather than adrenal medullary catecholamines, for lipid mobilization from WAT.

Indexed as

Lipid MobilizationAdipose Tissue, WhiteAdrenal GlandsAnimalsBody WeightCatecholaminesCricetinaeEnergy IntakeFood DeprivationHerpesvirus 1, SuidLipid MetabolismMaleParaventricular Hypothalamic NucleusPhodopusSympathetic Nervous SystemCatecholamines

Identifiers

PMID19851310
PMCPMC4002502
OpenAlexW2002296967

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.