Evidence map›Paper›PMID 19307753›Full record

ArticleExperimental & molecular medicine2009

Alterations of epinephrine-induced gluconeogenesis in aging.

Kyungtae Kim, Sung Chun Cho, Anthony Cova, Ik Soon Jang, Sang Chul Park

Open access · goldAbstract readComparative Study
In one paragraph

Article in Experimental & molecular medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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  3. Review
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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

5 authors at 3 institutions in 1 country.

Kyungtae KimDepartment of Biochemistry and Molecular Biology, The Aging and Apoptosis Research Center, Seoul National University, Korea.
Sung Chun Cho
Anthony Cova
Ik Soon Jang
Sang Chul Park
Seoul National University · KRKorea Basic Science Institute · KRNational Cancer Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The effects of glucagon and epinephrine on gluconeogenesis in young (4 month) and old (24 month) Fisher 344 rat hepatocytes were compared. In contrast to glucagon, which had a similar effect on gluconeogenesis in both young and old cells, epinephrine caused a smaller increase in gluconeogenesis in old rat hepatocytes than in young hepatocytes. beta2 adrenergic receptor (beta2-AR) expression slightly decreased in aged rat liver, and there were differences between young and old hepatocytes in their patterns of G protein coupled receptor kinases, which are involved in the activation of beta2-AR receptor signal desensitization. The major isoform of the kinase changed from GRK2 to GRK3 and the expression of beta-arrestin, which is recruited by the phosphorylated beta2-AR for internalization and degradation, increased in aged rat liver. GRK3 overexpression also decreased the glucose output from young rat hepatocytes. We conclude that an age-associated reduction in epinephrine-induced gluconeogenesis occurs through the epinephrine receptor desensitizing system.

Indexed as

GluconeogenesisAdrenergic beta-2 Receptor AgonistsAdrenergic beta-AgonistsAgingAnimalsEpinephrineGlucagonG-Protein-Coupled Receptor Kinase 2G-Protein-Coupled Receptor Kinase 3MaleModels, BiologicalPhosphorylationRatsRats, Inbred F344Receptors, Adrenergic, beta-2Adrenergic beta-2 Receptor AgonistsAdrenergic beta-AgonistsEpinephrineGlucagonG-Protein-Coupled Receptor Kinase 2G-Protein-Coupled Receptor Kinase 3Receptors, Adrenergic, beta-2

Identifiers

PMID19307753
PMCPMC2701982
OpenAlexW1989076547

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.