Evidence map›Paper›PMID 29311930›Full record

ArticleFrontiers in pharmacology2017

Orientin Reduces Myocardial Infarction Size via eNOS/NO Signaling and Thus Mitigates Adverse Cardiac Remodeling.

Fangfang Li, Jing Zong, Hao Zhang, Peijie Zhang, Luhong Xu, Kai Liang, Lu Yang, Hui Yong, Wenhao Qian

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Targeting L-arginine/NO/cGMP/KFrontiers in pharmacology · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Micro-Executor of Natural Products in Metabolic Diseases.Molecules (Basel, Switzerland) · 2023
    Review
  11. Article
  12. Orientin Prolongs the Longevity ofOxidative medicine and cellular longevity · 2022
    Article
  13. Article
  14. Article
  15. Advances in the Protective Mechanism of NO, HFrontiers in cardiovascular medicine · 2020
    Review
  16. Review
  17. CXCL16 is activated by p-JNK and is involved in HAmerican journal of translational research · 2018
    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

9 authors at 1 institution in 1 country.

Fangfang LiDepartment of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Jing ZongDepartment of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Hao ZhangDepartment of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Peijie ZhangEmergency Department, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Luhong XuDepartment of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Kai LiangDepartment of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Lu YangDepartment of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Hui YongDepartment of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Wenhao QianDepartment of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Xuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Orientin is a flavonoid extracted from Chinese traditional herb, Polygonum orientale L. Previous study has reported that orientin protected myocardial from ischemia reperfusion injury. However, whether orientin could protect against cardiac remodeling after myocardial injury remains unclear. The aim of our study is to investigate the effects of orientin in the progression of cardiac remodeling after myocardial infarction (MI). Mice cardiac remodeling model was established by left coronary artery ligation surgery. Experimental groups were as follows: vehicle-sham, orientin-sham, vehicle-MI, and orientin-MI. Animals were treated with vehicle or orientin (40 mg/kg) for 25 days starting 3 days after surgery. After 4 weeks of MI, mice with orientin treatment had decreased mortality and improved cardiac function. Significantly, at 4 weeks post-MI, orientin treatment decreased fibrosis, inflammatory response, and cardiomyocyte apoptosis. Furthermore, orientin treatment attenuated the hypoxia-induced neonatal rat cardiomyocyte apoptosis and increased cell viability. Additionally, orientin supplementation mitigated oxidative stress in remodeling heart tissue and cardiomyocytes exposed to hypoxia as measured by 2',7'-dichlorodihydrofluorescein diacetate fluorescent probe. Mechanistically, orientin promotes cardioprotection by activating the eNOS/NO signaling cascades, which was confirmed by eNOS inhibitor (L-NAME)

Indexed as

cardiac remodelingeNOSmyocardial infarctionnitric oxideorientinreactive oxygen species

Identifiers

PMID29311930
PMCPMC5742593
OpenAlexW2780759145

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.