Evidence map›Paper›PMID 26161243›Full record

ArticleOxidative medicine and cellular longevity2015

Ginsenoside Rb1 Treatment Attenuates Pulmonary Inflammatory Cytokine Release and Tissue Injury following Intestinal Ischemia Reperfusion Injury in Mice.

Ying Jiang, Zhen Zhou, Qing-tao Meng, Qian Sun, Wating Su, Shaoqing Lei, Zhengyuan Xia, Zhong-yuan Xia

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. CanJournal of ginseng research · 2022
    Review
  8. Article
  9. Oxidative Stress and Ginsenosides: An Update on the Molecular Mechanisms.Oxidative medicine and cellular longevity · 2022
    Review
  10. Review of the risk factors for SARS-CoV-2 transmission.World journal of clinical cases · 2021
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Ying JiangDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Zhen ZhouDepartment of Cardiovascular Surgery, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Qing-tao MengDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Qian SunDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Wating SuDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Shaoqing LeiDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Zhengyuan XiaDepartment of Anesthesiology, The University of Hong Kong, Pok Fu Lam, Hong Kong ; Department of Anesthesiology, Affiliated Hospital of Guangdong Medical College, Zhanjiang, Guangdong 524001, China.
Zhong-yuan XiaDepartment of Anesthesiology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Wuhan University · CNGuangdong Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective. Intestinal ischemia reperfusion (II/R) injury plays a critical role in remote organ dysfunction, such as lung injury, which is associated with nuclear factor erythroid 2-related factor 2 (Nrf2)/heme oxygenase-1 (HO-1) signaling pathway. In the present study, we tested whether ginsenoside Rb1 attenuated II/R induced lung injury by Nrf2/HO-1 pathway. Methods. II/R injury was induced in male C57BL/6J mice by 45 min of superior mesenteric artery (SMA) occlusion followed by 2 hours of reperfusion. Ginsenoside Rb1 was administrated prior to reperfusion with or without ATRA (all-transretinoic acid, the inhibitor of Nrf2/ARE signaling pathway) administration before II/R. Results. II/R induced lung histological injury, which is accompanied with increased levels of malondialdehyde (MDA), interleukin- (IL-) 6, and tumor necrosis factor- (TNF-) α but decreased levels of superoxide dismutase (SOD) and IL-10 in the lung tissues. Ginsenoside Rb1 reduced lung histological injury and the levels of TNF-α and MDA, as well as wet/dry weight ratio. Interestingly, the increased Nrf2 and HO-1 expression induced by II/R in the lung tissues was promoted by ginsenoside Rb1 treatment. All these changes could be inhibited or prevented by ATRA. Conclusion. Ginsenoside Rb1 is capable of ameliorating II/R induced lung injuries by activating Nrf2/HO-1 pathway.

Indexed as

AnimalsGinsenosidesHeme Oxygenase-1Interleukin-10Interleukin-6IntestinesLungMaleMalondialdehydeMiceMice, Inbred C57BLNF-E2-Related Factor 2Reperfusion InjurySignal TransductionSuperoxide DismutaseTretinoinginsenoside Rb1GinsenosidesHeme Oxygenase-1Interleukin-10Interleukin-6MalondialdehydeNF-E2-Related Factor 2Superoxide DismutaseTretinoinTumor Necrosis Factor-alpha

Identifiers

PMID26161243
PMCPMC4487341
OpenAlexW1525965209

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.