Evidence map›Paper›PMID 24400153›Full record

ArticlePhysiological reports2013

Cardioprotective effects of angiotensin III against ischemic injury via the AT2 receptor and KATP channels.

Byung Mun Park, Shan Gao, Seung Ah Cha, Byung Hyun Park, Suhn Hee Kim

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. The Level and Significance of Circulating Angiotensin-III in Patients with Coronary Atherosclerosis.Journal of the renin-angiotensin-aldosterone system : JRAAS · 2021
    Article
  4. The renin-angiotensin-aldosterone system and its suppression.Journal of veterinary internal medicine · 2019
    Review
  5. Review
  6. The role of KActa pharmacologica Sinica · 2018
    Review
  7. Review
  8. Comparative effects of angiotensin II and angiotensin-(4-8) on blood pressure and ANP secretion in rats.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2017
    Article
  9. Article
  10. Article
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 1 institution in 1 country.

Byung Mun ParkDepartment of Physiology, Research Institute for Endocrine Sciences, Chonbuk National University Medical School Jeonju, Korea.
Shan GaoDepartment of Physiology, Research Institute for Endocrine Sciences, Chonbuk National University Medical School Jeonju, Korea.
Seung Ah ChaDepartment of Physiology, Research Institute for Endocrine Sciences, Chonbuk National University Medical School Jeonju, Korea.
Byung Hyun ParkDepartment of Biochemistry, Research Institute for Endocrine Sciences, Chonbuk National University Medical School Jeonju, Korea.
Suhn Hee KimDepartment of Physiology, Research Institute for Endocrine Sciences, Chonbuk National University Medical School Jeonju, Korea.
Jeonbuk National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiotensin III (Ang III) has similar effects on blood pressure and aldosterone secretion as Ang II, but cardioprotective effects are also proposed. In this study, we investigated whether Ang III protects the heart against ischemia/reperfusion (I/R) injury. After sacrificing Sprague-Dawley rats, the hearts were perfused with Krebs-Henseleit buffer for a 20 min preischemic period with and without Ang III followed by 20-min global ischemia and 50-min reperfusion. Pretreatment with Ang III (1 μmol/L) improved an increased postischemic left ventricular end-diastolic pressure (LVEDP) and a decreased postischemic left ventricular developed pressure (LVDP) induced by reperfusion compared to untreated hearts. Ang III markedly decreased infarct size and lactate dehydrogenase levels in effluent during reperfusion. Ang III increased coronary flow and the concentrations of atrial natriuretic peptide in coronary effluent during reperfusion. Pretreatment with Ang II type 2 receptor (AT2R) antagonist or ATP-sensitive K(+) channel (KATP) blocker for 15 min before ischemia attenuated the improvement of LVEDP, LVDP, and ±dP/dt induced by Ang III. Ang III treatment increased Mn-superoxide dismutase, catalase, and heme oxygenase-1 protein levels, which was attenuated by pretreatment with AT2R antagonist or KATP blocker. Ang III treatment also decreased Bax, caspase-3, and caspase-9 protein levels, and increased Bcl-2 protein level, which were attenuated by pretreatment with AT2R antagonist or KATP blocker. These results suggest that the cardioprotective effects of Ang III against I/R injury may be partly related to activating antioxidant and antiapoptotic enzymes via AT2R and KATP channels.

Indexed as

Angiotensin IIIapoptosisatrial natriuretic peptideBaxBcl-2caspase-3caspase-9catalaseheartheme oxygenase-1ischemiaKATP channelsuperoxide dismutase

Identifiers

PMID24400153
PMCPMC3871466
OpenAlexW2060873615

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.