Evidence map›Paper›PMID 26092427›Full record

ArticleMolecular and cellular biochemistry2015

Genistein ameliorates cardiac inflammation and oxidative stress in streptozotocin-induced diabetic cardiomyopathy in rats.

Suresh K Gupta, Shirish Dongare, Rajani Mathur, Ipseeta Ray Mohanty, Sushma Srivastava, Sandeep Mathur, Tapas C Nag

Abstract read
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In one paragraph

Article in Molecular and cellular biochemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 3 pooled it
6.5field-weighted citation impact, top 3% 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

46 citing papers in PubMed, 3 syntheses or guidelines pooled it, 108 citations in OpenAlex.

  1. Pooled it
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  16. Multi-omics reveals the mechanisms underlyingAnimal nutrition (Zhongguo xu mu shou yi xue hui) · 2023
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  17. Review
  18. Review
  19. Review
  20. Pharmacological Effects of Genistein on Cardiovascular Diseases.Evidence-based complementary and alternative medicine : eCAM · 2023
    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

7 authors at 3 institutions in 1 country.

Suresh K GuptaDepartment of Pharmacology, Delhi Institute of Pharmaceutical Sciences and Research, Pushp Vihar, Sec. -3, New Delhi, 110017, India. skgup@hotmail.com.
Shirish DongareDepartment of Pharmacology, Delhi Institute of Pharmaceutical Sciences and Research, Pushp Vihar, Sec. -3, New Delhi, 110017, India.
Rajani MathurDepartment of Pharmacology, Delhi Institute of Pharmaceutical Sciences and Research, Pushp Vihar, Sec. -3, New Delhi, 110017, India.
Ipseeta Ray MohantyDepartments of Pharmacology, MGM Medical College, Navi Mumbai, India.
Sushma SrivastavaDepartment of Pharmacology, Delhi Institute of Pharmaceutical Sciences and Research, Pushp Vihar, Sec. -3, New Delhi, 110017, India.
Sandeep MathurDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Tapas C NagDepartment of Anatomy, All India Institute of Medical Sciences, New Delhi, India.
Delhi Pharmaceutical Science and Research University · INAll India Institute of Medical Sciences · INMahatma Gandhi Mission's Dental College and Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study was undertaken to evaluate the protective effects of genistein against cardiac inflammation and oxidative stress in streptozotocin (STZ) (45 mg/kg body weight)-induced diabetic rats. genistein (300 mg/kg/day) was administered orally for 24 weeks to STZ-induced diabetic rats. The effects of genistein on blood glucose, % glycosylated hemoglobin (HbA1c), C-reactive protein, tumor necrosis factor (TNF- α), transforming growth factor (TGF-β1), and total antioxidant were studied. Ultrastructural and histopathological assessment of injury were also undertaken using transmission electron microscope. STZ-induced diabetes resulted in significant increase in the levels of blood glucose, HbA1c, C-reactive protein, TNF- α and TGF-β1, and a decline in total antioxidant reserve of the myocardium. Administration of genistein to diabetic rats resulted in a decrease in blood glucose (p < 0.001), % HbA1c (p < 0.0001), C-reactive protein (p < 0.001), and expression of TNF- α (p < 0.001) and TGF-β1 (p < 0.0001) proteins. In addition, genistein treatment results in augmentation of total antioxidant (p < 0.01) reserve of the hearts. The above findings were supported by histological as well as immunohistochemical localization of NF-κB (p65) in the heart. Genistein treatment ameliorated the ultrastructural degenerative changes in the cardiac tissues as compared to the diabetic control. The result demonstrates that genistein restored the integrity of the diabetic myocardium by virtue of its anti-inflammatory and antioxidant effects.

Indexed as

Administration, OralAnimalsBiomarkersBlood GlucoseCardiomyopathiesC-Reactive ProteinDiabetes Mellitus, ExperimentalDrug Administration ScheduleGene Expression RegulationGenisteinGlycated HemoglobinOxidative StressRatsStreptozocinTransforming Growth Factor beta1Tumor Necrosis Factor-alphaBiomarkersBlood GlucoseC-Reactive ProteinGenisteinGlycated Hemoglobinhemoglobin A1c protein, humanStreptozocinTGFB1 protein, humanTNF protein, humanTransforming Growth Factor beta1Tumor Necrosis Factor-alphaDiabetic cardiomyopathyGenisteinInflammationOxidative stress

Identifiers

PMID26092427
OpenAlexW616481914

What OpenQuestion holds

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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.