Evidence map›Paper›PMID 22159884›Full record

ArticleDiabetologia2012

Increased metabolic rate and insulin sensitivity in male mice lacking the carcino-embryonic antigen-related cell adhesion molecule 2.

P R Patel, S K Ramakrishnan, M K Kaw, C K Raphael, S Ghosh, J S Marino, G Heinrich, S J Lee, R E Bourey, J W Hill and 6 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Diabetologia, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  6. Review
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  8. Article
  9. Neural immunoglobulin superfamily interaction networks.Current opinion in neurobiology · 2017
    Review
  10. Article
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  12. Article
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  14. Article
4 · The record

Corrections and comments

  • Erratum issued
    Rahmouni, S K [corrected to Rahmouni, K]
5 · Who and what money

Authors and funding

16 authors at 3 institutions in 1 country.

P R PatelCenter for Diabetes and Endocrine Research, College of Medicine and Life Sciences, University of Toledo, Health Science Campus, 3000 Arlington Avenue, Mail Stop 1009, Toledo, OH 43614, USA.
S K Ramakrishnan
M K Kaw
C K Raphael
S Ghosh
J S Marino
G Heinrich
S J Lee
R E Bourey
J W Hill
D Y Jung
D A Morgan
J K Kim
K Rahmouni
S K Rahmouni
S M Najjar
University of Toledo · USPennsylvania State University · USUniversity of Iowa · US

Funding

Role of the brain Renin-Angiotensin Sys. in Cardiovas and Metabolic RegulationP01HL084207 · NHLBI · UNIVERSITY OF IOWA · PI GROBE, JUSTIN L · 2007 to 2022
$30.2M
Yale Mouse Metabolic Phenotyping CenterU24DK059635 · NIDDK · YALE UNIVERSITY · PI SHULMAN, GERALD I · 2001 to 2015
$8.9M
SUBSTRATES AND INSULIN RECEPTOR ENDOCYTOSISR01DK054254 · NIDDK · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI NAJJAR, SONIA M. · 2000 to 2021
$5.8M
UMass Mouse Metabolic Phenotyping CenterU24DK093000 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KIM, JASON K · 2011 to 2015
$2.1M
Interleukin-10 and Regulation of Skeletal Muscle Insulin ActionR01DK080756 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KIM, JASON K · 2008 to 2012
$1.6M
Insulin resistance in the pathogenesis of NASHR01DK083850 · NIDDK · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI NAJJAR, SONIA M. · 2009 to 2010
$749k
Hypothalamic leptin and insulin signals aligning metabolic state and fertilityR00HD056491 · NICHD · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI HILL, JENNIFER WOOTTON · 2009 to 2011
$740k
NHLBI NIH HHS HL084207NHLBI NIH HHS P01 HL084207NICHD NIH HHS R00 HD056491NIDDK NIH HHS R01 DK054254NIDDK NIH HHS R01DK054254NIDDK NIH HHS R01 DK080756NIDDK NIH HHS R01 DK083850NIDDK NIH HHS R01DK083850NIDDK NIH HHS R01-DK80756NIDDK NIH HHS U24 DK059635NIDDK NIH HHS U24 DK093000NIDDK NIH HHS U24-DK59635
6 · The paper itself

Abstract

aims/hypothesisThe carcino-embryonic antigen-related cell adhesion molecule (CEACAM)2 is produced in many feeding control centres in the brain, but not in peripheral insulin-targeted tissues. Global Ceacam2 null mutation causes insulin resistance and obesity resulting from hyperphagia and hypometabolism in female Ceacam2 homozygous null mutant mice (Cc2 [also known as Ceacam2](-/-)) mice. Because male mice are not obese, the current study examined their metabolic phenotype.

methodsThe phenotype of male Cc2(-/-) mice was characterised by body fat composition, indirect calorimetry, hyperinsulinaemic-euglycaemic clamp analysis and direct recording of sympathetic nerve activity.

resultsDespite hyperphagia, total fat mass was reduced, owing to the hypermetabolic state in male Cc2(-/-) mice. In contrast to females, male mice also exhibited insulin sensitivity with elevated β-oxidation in skeletal muscle, which is likely to offset the effects of increased food intake. Males and females had increased brown adipogenesis. However, only males had increased activation of sympathetic tone regulation of adipose tissue and increased spontaneous activity. The mechanisms underlying sexual dimorphism in energy balance with the loss of Ceacam2 remain unknown. CONCLUSIONS/

interpretationThese studies identified a novel role for CEACAM2 in the regulation of metabolic rate and insulin sensitivity via effects on brown adipogenesis, sympathetic nervous outflow to brown adipose tissue, spontaneous activity and energy expenditure in skeletal muscle.

Indexed as

Energy MetabolismInsulin ResistanceAdipogenesisAdipose Tissue, BrownAdiposityAnimalsCell Adhesion MoleculesFemaleGlycoproteinsHyperphagiaHypothalamusMaleMiceMice, Inbred C57BLMice, KnockoutMice, Mutant StrainsCeacam2 protein, mouseCell Adhesion MoleculesGlycoproteinsRNA, Messenger

Identifiers

PMID22159884
PMCPMC3272352
OpenAlexW2168984770

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.