Evidence map›Paper›PMID 38743190›Full record

ArticleJournal of bioenergetics and biomembranes2024

Dapagliflozin attenuates LPS-induced myocardial injury by reducing ferroptosis.

Ke Hu, Pin Jiang, Jiaxin Hu, Bing Song, Ya Hou, Jinxuan Zhao, Haiting Chen, Jun Xie

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of bioenergetics and biomembranes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Therapeutical progress in sepsis-induced cardiomyopathy.Frontiers in cardiovascular medicine · 2026
    Review
  5. Article
  6. Article
  7. Review
  8. 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

8 authors.

Ke Hu *The Affiliated Drum Tower Hospital of Nanjing Medical University, Nanjing, 210008, Jiangsu, China.
Pin Jiang *Department of General Medicine, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.
Jiaxin Hu *Cardiovascular Disease Center, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi Clinical College of Wuhan University, Enshi, 445000, Hubei, China.
Bing SongDepartment of Cardiology, National Cardiovascular Disease Regional Center for Anhui, the First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.
Ya HouDepartment of Cardiology, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, MOE Key Laboratory of Model Animal for Disease Study, Nanjing University, Nanjing, 210008, Jiangsu, China.
Jinxuan ZhaoDepartment of Cardiology, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, MOE Key Laboratory of Model Animal for Disease Study, Nanjing University, Nanjing, 210008, Jiangsu, China. njuzhaojinxuan@163.com.
Haiting ChenDepartment of Cardiology, National Cardiovascular Disease Regional Center for Anhui, the First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China. cht141230004@163.com.
Jun XieThe Affiliated Drum Tower Hospital of Nanjing Medical University, Nanjing, 210008, Jiangsu, China. xiejun@ahmu.edu.cn.

Funding

Anhui Medical University Research Enhancement Program Funding Project 2023xkjT029Anhui Provincial Natural Science Research Project for Higher Education Institutions KJ2021ZD0027China Postdoctoral Science Foundation 2023M731631Collaborative Project between the First Affiliated Hospital of Anhui Medical University and Hefei Zhongke Ion Medical Technology Equipment Co., Ltd. CIM-HT-2018-327the Funds for Distinguished Young Scientists in Nanjing JQX22001the Jiangsu Distinguished Young Scholars Fund BK20211501the National Natural Science Foundation of China 92068116
6 · The paper itself

Abstract

Septic cardiomyopathy is a severe cardiovascular disease with a poor prognosis. Previous studies have reported the involvement of ferroptosis in the pathogenesis of septic cardiomyopathy. SGLT2 inhibitors such as dapagliflozin have been demonstrated to improve ischemia-reperfusion injury by alleviating ferroptosis in cardiomyocyte. However, the role of dapagliflozin in sepsis remains unclear. Therefore, our study aims to investigate the therapeutic effects of dapagliflozin on LPS-induced septic cardiomyopathy. Our results indicate that dapagliflozin improved cardiac function in septic cardiomyopathy experimental mice. Mechanistically, dapagliflozin works by inhibiting the translation of key proteins involved in ferroptosis, such as GPX4, FTH1, and SLC7A11. It also reduces the transcription of lipid peroxidation-related mRNAs, including PTGS2 and ACSL4, as well as iron metabolism genes TFRC and HMOX1.

Indexed as

Benzhydryl CompoundsFerroptosisGlucosidesLipopolysaccharidesAmino Acid Transport System y+AnimalsCardiomyopathiesMaleMiceMice, Inbred C57BLMyocytes, CardiacPhospholipid Hydroperoxide Glutathione PeroxidaseAmino Acid Transport System y+Benzhydryl CompoundsdapagliflozinGlucosidesglutathione peroxidase 4, mouseLipopolysaccharidesPhospholipid Hydroperoxide Glutathione PeroxidaseSlc7a11 protein, mouseCardiomyopathyDapagliflozinFerroptosisLipopolysaccharide

Identifiers

What OpenQuestion holds

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Registered trials

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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.