Evidence map›Paper›PMID 29522447›Full record

ReviewInternational journal of molecular sciences2018

The Inside Story of Adenosine.

Marcella Camici, Mercedes Garcia-Gil, Maria Grazia Tozzi

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 88 citations in OpenAlex.

  1. Article
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  15. Article
  16. Purinergic Signaling in Non-Parenchymal Liver Cells.International journal of molecular sciences · 2024
    Review
  17. Article
  18. 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

3 authors at 1 institution in 1 country.

Marcella CamiciDipartimento di Biologia, Unità di Biochimica, Via San Zeno 51, 56127 Pisa, Italy. marcella.camici@unipi.it.ORCID 0000-0001-8133-8414
Mercedes Garcia-GilDipartimento di Biologia, Unità di Fisiologia Generale, Via San Zeno 31, 56127 Pisa, Italy. mercedes.garcia@unipi.it.ORCID 0000-0002-1344-2786
Maria Grazia TozziDipartimento di Biologia, Unità di Biochimica, Via San Zeno 51, 56127 Pisa, Italy. maria.grazia.tozzi@unipi.it.ORCID 0000-0002-1075-7096
Istituto di Fisiologia Clinica · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several physiological functions of adenosine (Ado) appear to be mediated by four G protein-coupled Ado receptors. Ado is produced extracellularly from the catabolism of the excreted ATP, or intracellularly from AMP, and then released through its transporter. High level of intracellular Ado occurs only at low energy charge, as an intermediate of ATP breakdown, leading to hypoxanthine production. AMP, the direct precursor of Ado, is now considered as an important stress signal inside cell triggering metabolic regulation through activation of a specific AMP-dependent protein kinase. Intracellular Ado produced from AMP by allosterically regulated nucleotidases can be regarded as a stress signal as well. To study the receptor-independent effects of Ado, several experimental approaches have been proposed, such as inhibition or silencing of key enzymes of Ado metabolism, knockdown of Ado receptors in animals, the use of antagonists, or cell treatment with deoxyadenosine, which is substrate of the enzymes acting on Ado, but is unable to interact with Ado receptors. In this way, it was demonstrated that, among other functions, intracellular Ado modulates angiogenesis by regulating promoter methylation, induces hypothermia, promotes apoptosis in sympathetic neurons, and, in the case of oxygen and glucose deprivation, exerts a cytoprotective effect by replenishing the ATP pool.

Indexed as

Energy MetabolismAdenosineAdenosine DeaminaseAdenosine KinaseAdenosine MonophosphateAdenosine TriphosphateAnimalsApoptosisHumansHypothermiaMiceReceptors, Purinergic P1AdenosineAdenosine DeaminaseAdenosine KinaseAdenosine MonophosphateAdenosine TriphosphateReceptors, Purinergic P1adenosineadenosine deaminaseadenosine kinaseadenosine receptorsdeoxyadenosineenergy repletiontransmethylation

Identifiers

PMID29522447
PMCPMC5877645
OpenAlexW2791254798

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.