Evidence map›Paper›PMID 24599747›Full record

ArticleMolecular and cellular biochemistry2014

Apelin-12 and its structural analog enhance antioxidant defense in experimental myocardial ischemia and reperfusion.

O I Pisarenko, V Z Lankin, G G Konovalova, L I Serebryakova, V S Shulzhenko, A A Timoshin, O V Tskitishvili, Yu A Pelogeykina, I M Studneva

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biochemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 56 citations in OpenAlex.

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  12. Review
  13. Apelinergic System Structure and Function.Comprehensive Physiology · 2017
    Review
  14. 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

9 authors at 1 institution in 1 country.

O I PisarenkoLaboratory for Myocardial Metabolism, Russian Cardiology Research-and-Production Complex, 3rd Cherepkovskaya Str., 15A, 121552, Moscow, Russian Federation, olpi@live.ru.
V Z Lankin
G G Konovalova
L I Serebryakova
V S Shulzhenko
A A Timoshin
O V Tskitishvili
Yu A Pelogeykina
I M Studneva
Institute of Experimental Cardiology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated the effects of peptide apelin-12 (H-Arg-Pro-Arg-Leu-Ser-His-Lys-Gly-Pro-Met-Pro-Phe-OH, A12) and its novel structural analog (H-(N(α)Me)Arg-Pro-Arg-Leu-Ser-His-Lys-Gly-Pro-Nle-Pro-Phe-OH, AI) on myocardial antioxidant enzyme activities, lipid peroxidation, and reactive oxygen species formation in ex vivo and in vivo models of myocardial ischemia/reperfusion (I/R) injury. Isolated working rat hearts were subjected to global ischemia and reperfusion. Infusion of 140 μM A12 or AI before global ischemia improved cardiac function recovery; increased the activity of Cu,Zn superoxide dismutase (Cu,Zn SOD), catalase (CAT), and glutathione peroxidase (GSH-Px); decreased malondialdehyde (MDA) content in reperfused heart; and reduced the formation of hydroxyl radical adduct of the spin trap 5,5-dimethyl-1-pyrroline-N-oxide in the myocardial effluent during early reperfusion compared with these indices in control. Anesthetized open-chest rats were subjected to the left anterior descending coronary artery occlusion and coronary reperfusion. Peptide A12 or its analog AI was injected intravenously at the onset of reperfusion at a dose of 0.35 μmol/kg. Treatment with A12 or AI significantly limited infarct size and reduced the activity of lactate dehydrogenase and creatine kinase MB isoenzyme in blood plasma at the end of reperfusion compared with control. These effects were accompanied by complete recovery of Cu,Zn SOD, CAT, and GSH-Px activities; and decrease in MDA content in the area at risk by the end of reperfusion. The study concluded that C-terminal fragment of native peptide apelin-12 and its synthesized analog is involved in the upregulation of cardiac antioxidant defense systems and attenuation of lipid peroxidation in myocardial I/R injury.

Indexed as

AnesthesiaAnimalsAntioxidantsBiomarkersCatalaseCreatine Kinase, MB FormCyclic N-OxidesDisease Models, AnimalElectron Spin Resonance SpectroscopyGlutathione PeroxidaseIntercellular Signaling Peptides and ProteinsIn Vitro TechniquesL-Lactate DehydrogenaseMaleMalondialdehydeMyocardial Reperfusion Injury5,5-dimethyl-1-pyrroline-1-oxideAntioxidantsapelin-12 peptideBiomarkersCatalaseCreatine Kinase, MB FormCyclic N-OxidesGlutathione PeroxidaseIntercellular Signaling Peptides and ProteinsL-Lactate DehydrogenaseMalondialdehydeSuperoxide Dismutase

Identifiers

PMID24599747
PMCPMC7102085
OpenAlexW2140762593

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.