Evidence map›Paper›PMID 22016516›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

The metabolic regulator PGC-1α directly controls the expression of the hypothalamic neuropeptide oxytocin.

Janna Blechman, Liat Amir-Zilberstein, Amos Gutnick, Shifra Ben-Dor, Gil Levkowitz

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.4field-weighted citation impact, top 23% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Developmental Effects of Oxytocin Neurons on Social Affiliation and Processing of Social Information.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Serum Irisin and Oxytocin Levels as Predictors of Metabolic Parameters in Obese Children.Journal of clinical research in pediatric endocrinology · 2017
    Article
  14. Article
  15. Article
  16. Review
  17. The influences of parental diet and vitamin E intake on the embryonic zebrafish transcriptome.Comparative biochemistry and physiology. Part D, Genomics & proteomics · 2014
    Article
  18. Article
  19. Role of oxytocin signaling in the regulation of body weight.Reviews in endocrine & metabolic disorders · 2013
    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

5 authors at 2 institutions in 2 countries.

Janna BlechmanDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot 76100, Israel.
Liat Amir-Zilberstein
Amos Gutnick
Shifra Ben-Dor
Gil Levkowitz
Institute of Molecular and Cell Biology · RUWeizmann Institute of Science · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transcriptional coactivator PGC-1α is a key regulator of cellular energy expenditure in peripheral tissues. Recent studies report that PGC-1α-null mice develop late-onset obesity and that the neuronal inactivation of PGC-1α causes increased food intake. However, the exact role of PGC-1α in the CNS remains unclear. Here we show that PGC-1α directly regulates the expression of the hypothalamic neuropeptide oxytocin, a known central regulator of appetite. We developed a unique genetic approach in the zebrafish, allowing us to monitor and manipulate PGC-1α activity in oxytocinergic neurons. We found that PGC-1α is coexpressed with oxytocin in the zebrafish hypothalamus. Targeted knockdown of the zebrafish PGC-1α gene activity caused a marked decrease in oxytocin mRNA levels and inhibited the expression of a transgenic GFP reporter driven by the oxytocin promoter. The effect of PGC-1α loss of function on oxytocin gene activity was rescued by tissue-specific re-expression of either PGC-1α or oxytocin precursor in zebrafish oxytocinergic neurons. PGC-1α activated the oxytocin promoter in a heterologous cell culture system, and overexpression of PGC-1α induced ectopic expression of oxytocin in muscles and neurons. Finally, PGC-1α forms an in vivo complex with the oxytocin promoter in fed but not fasted animals. These findings demonstrate that PGC-1α is both necessary and sufficient for the production of oxytocin, implicating hypothalamic PGC-1α in the direct activation of a hypothalamic hormone known to control energy intake.

Indexed as

Analysis of VarianceAnimalsAnimals, Genetically ModifiedCell Line, TransformedChromatin ImmunoprecipitationComputational BiologyEmbryo, NonmammalianFastingFeeding BehaviorGene Expression Regulation, DevelopmentalGreen Fluorescent ProteinsHeat-Shock ProteinsHumansHypothalamusMaleMiceenhanced green fluorescent proteinGreen Fluorescent ProteinsHeat-Shock ProteinsOligodeoxyribonucleotides, AntisenseOxytocinPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPARGC1A protein, humanRNA, MessengerTranscription Factors

Identifiers

PMID22016516
PMCPMC6623572
OpenAlexW2001486453

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.