Evidence map›Paper›PMID 39583164›Full record

ArticleJournal of ginseng research2024

Ginsenoside Rg1 reduces cardiac inflammation against myocardial ischemia/reperfusion injury by inhibiting macrophage polarization.

Xiaojin Xu, Qing Wu, Ke Pei, Meng Zhang, Chenhan Mao, Xinxin Zhong, Yunfan Huang, Yang Dai, Rui Yin, Zhaoyang Chen and 1 more

Abstract read
In one paragraph

Article in Journal of ginseng research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Ginsenosides fromJournal of ginseng research · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Components ofFrontiers in pharmacology · 2026
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. 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

11 authors.

Xiaojin XuThe Third Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, China.
Qing WuSchool of Integrated Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
Ke PeiSchool of Integrated Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
Meng ZhangShuguang Hospital Affiliated to Shanghai University of Chinese Medicine, Shanghai, China.
Chenhan MaoThe Third Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, China.
Xinxin ZhongSchool of Integrated Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
Yunfan HuangSchool of Integrated Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
Yang DaiThe Third Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, China.
Rui YinThe Third Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, China.
Zhaoyang ChenThe Third Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, China.
Xindong WangThe Third Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Myocardial ischemia/reperfusion (MI/R) injury is the main cause of death worldwide and poses a significant threat to cardiac health. Ginsenoside Rg1 has been shown to have inhibitory effects on inflammatory activation, oxidative stress, and cardiac injury, suggesting that Rg1 may have therapeutic effects on MI/R injury. However, the mechanism remains to be further studied. Materials and methods: Left anterior descending coronary artery ligation was performed in Sprague-Dawley rats to construct an MI/R model Results: Administration of Rg1 exhibited dose-dependent cardioprotective effects and effectively reduced MI/R injury. Rg1 significantly attenuated myocardial inflammation and inhibited M1 macrophage polarization during MI/R injury. Furthermore, Rg1 significantly reduced cardiac fibrosis in response to MI/R injury. This anti-fibrotic effect may contribute to the preservation of cardiac structure and function following an ischemic insult. Meanwhile, Rg1 effectively inhibited the activation of the AIM2 inflammasome Conclusion: Our findings elucidate the multifaceted mechanisms underlying Rg1's cardioprotective effects, including its ability to mitigate inflammation, modulate macrophage polarization, and inhibit fibrosis.

Indexed as

AIM2 inflammasomeCardiac fibrosisGinsenoside Rg1Macrophage polarizationMyocardial ischemia-reperfusion injury (MIRI)

Identifiers

PMID39583164
PMCPMC11583468

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.