Evidence map›Paper›PMID 37603159›Full record

ArticleInflammopharmacology2023

Anti-inflammatory, cardioprotective effect of gypenoside against isoproterenol-induced cardiac remodeling in rats via alteration of inflammation and gut microbiota.

Xuemei Zhang, Ying Zhao, Xin Zhao, Ji Zhang, Jiayu Diao, Shuo Jia, Panpan Feng, Penghua Yu, Gong Cheng

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammopharmacology, 2023. 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
4.0field-weighted citation impact, top 7% 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, 10 citations in OpenAlex.

  1. Article
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  5. Article
  6. Review
  7. Article
  8. Article
  9. Cardioprotective effects ofFrontiers in pharmacology · 2025
    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.

Xuemei ZhangUltrasonic Diagnosis Center, Shaanxi Provincial People's Hospital, Xi'an, 710068, China.
Ying ZhaoUltrasonic Diagnosis Center, Shaanxi Provincial People's Hospital, Xi'an, 710068, China.
Xin ZhaoUltrasonic Diagnosis Center, Shaanxi Provincial People's Hospital, Xi'an, 710068, China.
Ji ZhangDepartment of Emergency, Shaanxi Provincial People's Hospital, Xi'an, 710068, China.
Jiayu DiaoDepartment of Cardiology, Shaanxi Provincial People's Hospital, Xi'an, 710068, China.
Shuo JiaDepartment of Emergency, Shaanxi Provincial People's Hospital, Xi'an, 710068, China.
Panpan FengDepartment of General Medicine, Shaanxi Provincial People's Hospital, Xi'an, 710068, China.
Penghua YuDepartment of Cardiology, Shaanxi Provincial People's Hospital, Xi'an, 710068, China.
Gong ChengDepartment of Cardiology, Shaanxi Provincial People's Hospital, Xi'an, 710068, China. shanxichenggong@sina.com.ORCID http://orcid.org/0000-0002-3711-4760
Shanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyocardial infarction (MI), commonly referred to as a heart attack, occurs when the blood flow to a portion of the heart is blocked, causing damage to the heart muscle. In this study, we scrutinized the cardioprotective effect of gypenoside against the isoproterenol (ISO)-induced myocardial injury (MI) in the rats.

methodsWistar rats were divided into four groups as follow: normal, gypenoside (10 mg/kg), ISO control, and ISO control treated with the gypenoside (2.5, 5, and 10 mg/kg). Various parameters were estimated such as infract size, hemodynamic, inflammatory, antioxidant, cardiac, cytokines, and apoptotic markers. We also estimated the gut microbiota in the faces of the experimental rats. Finally, heart tissue histopathology performed.

resultDose-dependent treatment of gypenoside significantly (P < 0.001) reduced the infracted size along with suppression of the heart weight and heart ratio along with enhance the body weight. Gypenoside treatment considerably altered the level of cardiac parameters, cardiac membrane stabilizing enzyme, hemodynamic parameters, antioxidant, lipid parameters, hepatic parameters, renal parameters, inflammatory cytokines, and mediators. Gypenoside significantly (P < 0.001) suppressed the level of apoptotic markers such as caspase-3, caspase-6, and caspase-9. Gypenoside significantly (P < 0.001) altered the relative abundance of unclassified bacteria, Tenericutes, Candidatus_Saccharibacteria, Verrucomicrobia, Actinobacteria, Bacteroidetes, Firmicutes and suppressed the ratio of F/B.

conclusionGypenoside acts as a protective phytoconstituents against the ISO-induced myocardial infraction in the rats via alteration of gut microbiota, inflammatory, and oxidative stress.

Indexed as

Gastrointestinal MicrobiomeMyocardial InfarctionAnimalsAnti-Inflammatory AgentsAntioxidantsApoptosisCytokinesGynostemmaInflammationIsoproterenolOxidative StressPlant ExtractsRatsRats, WistarVentricular RemodelingAnti-Inflammatory AgentsAntioxidantsCytokinesgypenosideIsoproterenolPlant ExtractsAntioxidantApoptosisCardiac toxicityGypenosideInflammation

Identifiers

PMID37603159
OpenAlexW4386019414

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.