Evidence map›Paper›PMID 24742672›Full record

ArticleThe Journal of biological chemistry2014

Divergent roles for adiponectin receptor 1 (AdipoR1) and AdipoR2 in mediating revascularization and metabolic dysfunction in vivo.

Jennifer L Parker-Duffen, Kazuto Nakamura, Marcy Silver, Maria A Zuriaga, Susan MacLauchlan, Tamar R Aprahamian, Kenneth Walsh

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Tumor-Associated Macrophage in Breast Tumor Microenvironment.International journal of molecular sciences · 2025
    Review
  4. Review
  5. Adiponectin Resistance in Obesity: Adiponectin Leptin/Insulin Interaction.Advances in experimental medicine and biology · 2024
    Review
  6. Article
  7. Review
  8. Article
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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

7 authors at 2 institutions in 1 country.

Jennifer L Parker-DuffenFrom the Whitaker Cardiovascular Institute, Department of Pharmacology and Experimental Therapeutics and.
Kazuto NakamuraFrom the Whitaker Cardiovascular Institute.
Marcy SilverFrom the Whitaker Cardiovascular Institute.
Maria A ZuriagaFrom the Whitaker Cardiovascular Institute.
Susan MacLauchlanFrom the Whitaker Cardiovascular Institute.
Tamar R AprahamianFrom the Whitaker Cardiovascular Institute, Department of Medicine-Renal Section, Boston University School of Medicine, Boston, Massachusetts 02118.
Kenneth WalshFrom the Whitaker Cardiovascular Institute, Department of Pharmacology and Experimental Therapeutics and kxwalsh@bu.edu.
Cardiovascular Institute of the South · USBoston University · US

Funding

Redox regulation in Endothelial Progenitor CellsP01HL081587 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WALSH, KENNETH · 2005 to 2015
$21.5M
SIRT1, Polyphenols, and Endothelial OxidantsP01HL068758 · NHLBI · BOSTON MEDICAL CENTER · PI WALSH, KENNETH · 2003 to 2013
$14.1M
Multidisciplinary Training in Cardiovascular ResearchT32HL007224 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI HAMBURG, NAOMI MIRIAM, WAINFORD, RICHARD DAVID · 1985 to 2020
$12.3M
TRAINING IN BIOMOLECULAR PHARMACOLOGYT32GM008541 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FARB, DAVID H · 1997 to 2022
$5.2M
Training Program in Cardiovascular Biology: Pre-DoctoralT32HL007969 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAVID, KATYA · 2003 to 2019
$3.2M
Anti-Angiogenic Mechanisms in Human ObesityR01HL126141 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GOKCE, NOYAN, WALSH, KENNETH · 2015 to 2019
$2.4M
Muscle loss and metabolic dysfunction associated with agingR01AG034972 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WALSH, KENNETH · 2010 to 2014
$1.6M
Role of PPARgamma signaling and adiponectin in Systemic Lupus ErythematosusK01AR055965 · NIAMS · BOSTON MEDICAL CENTER · PI APRAHAMIAN, TAMAR · 2009 to 2013
$645k
NHLBI NIH HHS HL007224NHLBI NIH HHS HL007969NHLBI NIH HHS HL68758NHLBI NIH HHS HL81587NHLBI NIH HHS P01 HL068758NHLBI NIH HHS P01 HL081587NHLBI NIH HHS R01 HL126141NHLBI NIH HHS T32 HL007224NHLBI NIH HHS T32 HL007969NIAMS NIH HHS K01 AR055965NIAMS NIH HHS K01 AR055965-02NIA NIH HHS AG34972NIA NIH HHS R01 AG034972NIGMS NIH HHS GM008541NIGMS NIH HHS T32 GM008541
6 · The paper itself

Abstract

Adiponectin is a well described anti-inflammatory adipokine that is highly abundant in serum. Previous reports have found that adiponectin deficiency promotes cardiovascular and metabolic dysfunction in murine models, whereas its overexpression is protective. Two candidate adiponectin receptors, AdipoR1 and AdipoR2, are uncharacterized with regard to cardiovascular tissue homeostasis, and their in vivo metabolic functions remain controversial. Here we subjected AdipoR1- and AdipoR2-deficient mice to chronic hind limb ischemic surgery. Blood flow recovery in AdipoR1-deficient mice was similar to wild-type; however, revascularization in AdipoR2-deficient mice was severely attenuated. Treatment with adiponectin enhanced the recovery of wild-type mice but failed to rescue the impairment observed in AdipoR2-deficient mice. In view of this divergent receptor function in the hind limb ischemia model, AdipoR1- and AdipoR2-deficient mice were also evaluated in a model of diet-induced obesity. Strikingly, AdipoR1-deficient mice developed severe metabolic dysfunction compared with wild type, whereas AdipoR2-deficient mice were protected from diet-induced weight gain and metabolic perturbations. These data show that AdipoR2, but not AdipoR1, is functionally important in an in vivo model of ischemia-induced revascularization and that its expression is essential for the revascularization actions of adiponectin. These data also show that, in contrast to revascularization responses, AdipoR1, but not AdipoR2 deficiency, leads to diet-induced metabolic dysfunction, revealing that these receptors have highly divergent roles in vascular and metabolic homeostasis.

Indexed as

Neovascularization, PhysiologicAnimalsExtremitiesMetabolic DiseasesMiceMice, KnockoutReceptors, Adiponectinadiponectin receptor 1, mouseadiponectin receptor 2, mouseReceptors, AdiponectinAdiponectinAdipoR1AdipoR2AngiogenesisMetabolismReceptorVascular Biology

Identifiers

PMID24742672
PMCPMC4047390
OpenAlexW2093181689

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.