Evidence map›Paper›PMID 18157164›Full record

ArticleBritish journal of pharmacology2008

Skeletal muscle expresses the extracellular cyclic AMP-adenosine pathway.

T Chiavegatti, V L Costa, M S Araújo, R O Godinho

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 62 citations in OpenAlex.

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  14. The 2',3'-cAMP-adenosine pathway.American journal of physiology. Renal physiology · 2011
    Review
  15. Article
  16. Extracellular cAMP-adenosine pathways in the mouse kidney.American journal of physiology. Renal physiology · 2011
    Article
  17. Article
  18. Endogenous luminal surface adenosine signaling regulates duodenal bicarbonate secretion in rats.The Journal of pharmacology and experimental therapeutics · 2010
    Article
  19. Extracellular 3',5'-cAMP-adenosine pathway inhibits glomerular mesangial cell growth.The Journal of pharmacology and experimental therapeutics · 2010
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

T ChiavegattiDepartment of Pharmacology, Universidade Federal de São Paulo-Escola Paulista de Medicina, Rua Três de Maio, São Paulo, SP, Brazil.
V L Costa
M S Araújo
R O Godinho
Universidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposecAMP is a key intracellular signalling molecule that regulates multiple processes of the vertebrate skeletal muscle. We have shown that cAMP can be actively pumped out from the skeletal muscle cell. Since in other tissues, cAMP efflux had been associated with extracellular generation of adenosine, in the present study we have assessed the fate of interstitial cAMP and the existence of an extracellular cAMP-adenosine signalling pathway in skeletal muscle. EXPERIMENTAL APPROACH: cAMP efflux and/or its extracellular degradation were analysed by incubating rat cultured skeletal muscle with exogenous cAMP, forskolin or isoprenaline. cAMP and its metabolites were quantified by radioassay or HPLC, respectively. KEY

resultsIncubation of cells with exogenous cAMP was followed by interstitial accumulation of 5'-AMP and adenosine, a phenomenon inhibited by selective inhibitors of ecto-phosphodiesterase (DPSPX) and ecto-nucleotidase (AMPCP). Activation of adenylyl cyclase (AC) in cultured cells with forskolin or isoprenaline increased cAMP efflux and extracellular generation of 5'-AMP and adenosine. Extracellular cAMP-adenosine pathway was also observed after direct and receptor-dependent stimulation of AC in rat extensor muscle ex vivo. These events were attenuated by probenecid, an inhibitor of ATP binding cassette family transporters. CONCLUSIONS AND IMPLICATIONS: Our results show the existence of an extracellular biochemical cascade that converts cAMP into adenosine. The functional relevance of this extracellular signalling system may involve a feedback modulation of cellular response initiated by several G protein-coupled receptor ligands, amplifying cAMP influence to a paracrine mode, through its metabolite, adenosine.

Indexed as

AdenosineAdenosine MonophosphateAdenosine TriphosphatasesAdenylyl CyclasesAnimalsChromatography, High Pressure LiquidCyclic AMPExtracellular SpaceLigandsMaleMuscle, SkeletalRadioligand AssayRatsRats, WistarReceptors, G-Protein-CoupledSignal TransductionAdenosineAdenosine MonophosphateAdenosine TriphosphatasesAdenylyl CyclasesCyclic AMPectoATPaseLigandsReceptors, G-Protein-Coupled

Identifiers

PMID18157164
PMCPMC2275449
OpenAlexW1496842742

What OpenQuestion holds

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Registered trials

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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.