Evidence map›Paper›PMID 9276726›Full record

ArticleThe Journal of clinical investigation1997

Targeted gene disruption reveals a leptin-independent role for the mouse beta3-adrenoceptor in the regulation of body composition.

J P Revelli, F Preitner, S Samec, P Muniesa, F Kuehne, O Boss, J D Vassalli, A Dulloo, J Seydoux, J P Giacobino and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

21 citing papers in PubMed, 97 citations in OpenAlex.

  1. Review
  2. The βAdvances in pharmacological and pharmaceutical sciences · 2024
    Review
  3. Review
  4. Is the βBiomolecules · 2023
    Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Adrenoceptors in white, brown, and brite adipocytes.British journal of pharmacology · 2019
    Review
  10. Article
  11. Article
  12. Article
  13. Polymorphism of the bovine ADRB3 gene.Molecular biology reports · 2010
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Old and new determinants in the regulation of energy expenditure.Journal of endocrinological investigation · 2002
    Review
  19. Article
  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

12 authors at 3 institutions in 3 countries.

J P RevelliDépartement de Biochimie Médicale, Centre Médical Universitaire, CH-1211 Genève 4, Switzerland.
F Preitner
S Samec
P Muniesa
F Kuehne
O Boss
J D Vassalli
A Dulloo
J Seydoux
J P Giacobino
J Huarte
C Ody
Centre de Biologie Structurale · FRUniversity of Geneva · CHZTE (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeted disruption of mouse beta3-adrenoceptor was generated by homologous recombination, and validated by an acute in vivo study showing a complete lack of effect of the beta3-adrenoceptor agonist CL 316,243 on the metabolic rate of homozygous null (-/-) mice. In brown adipose tissue, beta3-adrenoceptor disruption induced a 66% decrease (P < 0.005) in beta1-adrenoceptor mRNA level, whereas leptin mRNA remained unchanged. Chronic energy balance studies in chow-fed mice showed that in -/- mice, body fat accumulation was favored (+41%, P < 0.01), with a slight increase in food intake (+6%, NS). These effects were accentuated by high fat feeding: -/- mice showed increased total body fat (+56%, P < 0.025) and food intake (+12%, P < 0.01), and a decrease in the fat-free dry mass (-10%, P < 0.05), which reflects a reduction in body protein content. Circulating leptin levels were not different in -/- and control mice regardless of diet. The significant shift to the right in the positive correlation between circulating leptin and percentage of body fat in high fat-fed -/- mice suggests that the threshold of body fat content inducing leptin secretion is higher in -/- than in control mice. Taken together, these studies demonstrate that beta3-adrenoceptor disruption creates conditions which predispose to the development of obesity.

Indexed as

Body CompositionAdipose TissueAnimalsBlotting, NorthernBody Temperature RegulationCells, CulturedDietary FatsEnergy MetabolismLeptinMaleMiceProteinsReceptors, Adrenergic, betaReceptors, Adrenergic, beta-1Receptors, Adrenergic, beta-3Receptors, LeptinDietary FatsLeptinleptin receptor, mouseProteinsReceptors, Adrenergic, betaReceptors, Adrenergic, beta-1Receptors, Adrenergic, beta-3Receptors, Leptin

Identifiers

PMID9276726
PMCPMC508284
OpenAlexW2072147633

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.