Evidence map›Paper›PMID 26550459›Full record

ArticleAmerican journal of translational research2015

Eplerenone attenuates cardiac dysfunction and oxidative stress in β-receptor stimulated myocardial infarcted rats.

Navya M Reddy, Umesh B Mahajan, Chandragouda R Patil, Yogeeta O Agrawal, Shreesh Ojha, Sameer N Goyal

Abstract read
In one paragraph

Article in American journal of translational research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Navya M ReddyCardiovascular Pharmacology Division, Department of Pharmacology, R. C. Patel Institute of Pharmaceutical Education and Research Shirpur-Dist-Dhule, Maharashtra, India.
Umesh B MahajanCardiovascular Pharmacology Division, Department of Pharmacology, R. C. Patel Institute of Pharmaceutical Education and Research Shirpur-Dist-Dhule, Maharashtra, India.
Chandragouda R PatilCardiovascular Pharmacology Division, Department of Pharmacology, R. C. Patel Institute of Pharmaceutical Education and Research Shirpur-Dist-Dhule, Maharashtra, India.
Yogeeta O AgrawalDepartment of Pharmaceutics and Quality Assurance, R. C. Patel Institute of Pharmaceutical Education and Research Shirpur-Dist-Dhule, Maharashtra, India.
Shreesh OjhaDepartment of Pharmacology and Therapeutics College of Medicine and Health Sciences, United Arab Emirates University Al-Ain, United Arab Emirates.
Sameer N GoyalCardiovascular Pharmacology Division, Department of Pharmacology, R. C. Patel Institute of Pharmaceutical Education and Research Shirpur-Dist-Dhule, Maharashtra, India.
Shri Vile Parle Kelavani Mandal · INUnited Arab Emirates University · AE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eplerenone is a competitive antagonist of the aldosterone receptor with an additional PI3K-Akt activity. The existing cram has been intended to explore, whether eplerenone treatment attenuates the expansion of myocardial infarction in isoproterenol treated rats by restoring hemodynamic, biochemical, and histopathological changes. Isoproterenol induced cardiotoxicity was evidenced by marked ST elevation, decrease in systolic, diastolic, mean arterial pressures. Maximal positive rate of developed left ventricular pressure (+LVdP/dt max, a indicator of myocardial contraction), maximal negative rate of developed left ventricular pressure (-LVdP/dt max, a meter of myocardial relaxation) and an increase in left ventricular end-diastolic pressure (LVEDP, a marker of pre-load) were also shown. In addition, a significant reduction in activities of myocardial creatine kinase-MB isoenzyme, lactate dehydrogenase, superoxide dismutase, catalase, and reduced glutathione level along with increase in malondialdehyde content were observed. Oral pre-treatment with eplerenone (50, 100 and 150 mg/kg) daily for a period of 14 days, constructively modulated the studied parameters in isoproterenol-induced myocardial injury. The protective role of eplerenone on isoproterenolinduced myocardial damage was further confirmed by histopathological examinations. Eplerenone at doses of 100 mg/kg and 150 mg/kg produced more pronounced protective effects than 50 mg/kg body weight. Together, our study provides evidence for protective effects of eplerenone on myocardium in experimentally induced myocardial infarction.

Indexed as

EplerenoneisoproterenolLVEDPmyocardial infarctionST elevation

Identifiers

PMID26550459
PMCPMC4626421
OpenAlexW2157764926

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.