Evidence map›Paper›PMID 37143025›Full record

ArticleBMC endocrine disorders2023

Dual A

Olakunle Sanni, Gisella Terre'Blanche

Open access · goldAbstract read
In one paragraph

Article in BMC endocrine disorders, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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

2 authors at 1 institution in 1 country.

Olakunle SanniCentre of Excellence for Pharmaceutical Sciences (Pharmacen), School of Health Sciences, North-West University (NWU), Potchefstroom, 2357, South Africa. 37034898@nwu.ac.za.ORCID http://orcid.org/0000-0002-4924-9005
Gisella Terre'BlancheCentre of Excellence for Pharmaceutical Sciences (Pharmacen), School of Health Sciences, North-West University (NWU), Potchefstroom, 2357, South Africa.ORCID http://orcid.org/0000-0001-5586-3071
North-West University · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimRecent research suggests that adenosine receptors (ARs) influence many of the metabolic abnormalities associated with diabetes. A non-xanthine benzylidene indanone derivative 2-(3,4-dihydroxybenzylidene)-4-methoxy-2,3-dihydro-1 H-inden-1-one (2-BI), has shown to exhibit higher affinity at A

methodsThe study was designed to assess the antidiabetic effects of several A

resultsDual A

conclusion2-BI exhibited good antidiabetic activity by reducing intestinal postprandial glucose absorption and improving glucose tolerance in a diabetic animal model. The dual antagonism of A

Indexed as

Diabetes Mellitus, ExperimentalHyperglycemiaMetforminAdenosine A2 Receptor AntagonistsAnimalsBlood GlucoseCaffeineGlucoseHypoglycemic AgentsIndansMalePioglitazonePurinergic P1 Receptor AntagonistsRatsRats, Sprague-DawleyReceptor, Adenosine A12-benzylidene-1-indanoneAdenosine A2 Receptor AntagonistsBlood GlucoseCaffeineGlucoseHypoglycemic AgentsIndansMetforminPioglitazonePurinergic P1 Receptor AntagonistsReceptor, Adenosine A1StreptozocinAdenosine receptor antagonist, hyperglycemiaGlucose absorptionGlucose tolerance

Identifiers

PMID37143025
PMCPMC10157944
OpenAlexW4368367701

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.