Evidence map›Paper›PMID 17624709›Full record

ArticleExperimental gerontology2007

Adipogenic signaling in rat white adipose tissue: modulation by aging and calorie restriction.

Min Zhu, Garrick D Lee, Liusong Ding, Jingping Hu, Guang Qiu, Rafa de Cabo, Michel Bernier, Donald K Ingram, Sige Zou

Open access · greenAbstract read
In one paragraph

Article in Experimental gerontology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 71 citations in OpenAlex.

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  14. Sudden decrease in physical activity evokes adipocyte hyperplasia in 70- to 77-day-old rats but not 49- to 56-day-old rats.American journal of physiology. Regulatory, integrative and comparative physiology · 2013
    Article
  15. Article
  16. Review
  17. Article
  18. Diet and aging.Oxidative medicine and cellular longevity · 2012
    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

9 authors at 1 institution in 1 country.

Min ZhuLaboratory of Experimental Gerontology, National Institute on Aging, 6200 Seaforth Street, Baltimore, MD 21224, USA.
Garrick D Lee
Liusong Ding
Jingping Hu
Guang Qiu
Rafa de Cabo
Michel Bernier
Donald K Ingram
Sige Zou
National Institute on Aging · US

Funding

Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2005 to 2026
$26.5M
Calorie restriction and agingZ01AG000368 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 2005 to 2008
$1.4M
Functional Genomic Study of Aging and Aging InterventionsZ01AG000365 · NIA · NATIONAL INSTITUTE ON AGING · PI ZOU, SIGE · 2005 to 2008
$1.1M
REGULATION OF PHYSIOLOGICAL FUNCTIONS DURING AGING--III. BEHAVIORAL BIOLOGYZ01AG000302 · NIA · NATIONAL INSTITUTE ON AGING · PI DE CABO, RAFAEL · 1985 to 2008
$998k
Intramural NIH HHS Z01 AG000365NIDDK NIH HHS P30 DK072476
6 · The paper itself

Abstract

Alterations in adipogenesis could have significant impact on several aging processes. We previously reported that calorie restriction (CR) in rats significantly increases the level of circulating adiponectin, a distinctive marker of differentiated adipocytes, leading to a concerted modulation in the expression of key transcription target genes and, as a result, to increased fatty acid oxidation and reduced deleterious lipid accumulation in other tissues. These findings led us to investigate further the effects of aging on adipocytes and to determine how CR modulates adipogenic signaling in vivo. CR for 2 and 25 months, significantly increased the expression of PPARgamma, C/EBPbeta and Cdk-4, and partially attenuated age-related decline in C/EBPalpha expression relative to rats fed ad libitum (AL). As a result, adiponectin was upregulated at both mRNA and protein levels, resulting in activation of target genes involved in fatty acid oxidation and fatty acid synthesis, and greater responsiveness of adipose tissue to insulin. Moreover, CR significantly decreased the ratio of C/EBPbeta isoforms LAP/LIP, suggesting the suppression of gene transcription associated with terminal differentiation while facilitating preadipocytes proliferation. Morphometric analysis revealed a greater number of small adipocytes in CR relative to AL feeding. Immunostaining confirmed that small adipocytes were more strongly positive for adiponectin than the large ones. Overall these results suggest that CR increased the expression of adipogenic factors, and maintained the differentiated state of adipocytes, which is critically important for adiponectin biosynthesis and insulin sensitivity.

Indexed as

Caloric RestrictionAcyl-CoA OxidaseAdipogenesisAdiponectinAdipose Tissue, WhiteAgingAnimalsBase SequenceDNA PrimersFatty Acid Synthase, Type IInsulinLeptinMaleRatsRats, Inbred F344Receptor, InsulinAcyl-CoA OxidaseAdiponectinDNA PrimersFatty Acid Synthase, Type IInsulinLeptinReceptor, InsulinRNA, MessengerTranscription Factors

Identifiers

PMID17624709
PMCPMC1978194
OpenAlexW2089018784

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.