Evidence map›Paper›PMID 28193684›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2017

An Agonist of the Protective Factor SIRT1 Improves Functional Recovery and Promotes Neuronal Survival by Attenuating Inflammation after Spinal Cord Injury.

Haihong Chen, Hao Ji, Ming Zhang, Zude Liu, Lifeng Lao, Chao Deng, Jianwei Chen, Guibin Zhong

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 2% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
  2. Sirtuin1 modulates P53/Nrf2 pathway to promote spinal cord injury repair.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Nicotinamide Adenine Dinucleotide (NADAntioxidants & redox signaling · 2023
    Review
  11. Article
  12. Outcomes of RIP Kinase Signaling During Neuroinvasive Viral Infection.Current topics in microbiology and immunology · 2023
    Review
  13. Review
  14. Review
  15. Review
  16. Effect of Sirtuin-1 and Wnt/Computational and mathematical methods in medicine · 2022
    Article
  17. Article
  18. Review
  19. Article
  20. SIRT1 Promotes M2 Microglia PolarizationFrontiers in immunology · 2021
    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

8 authors at 2 institutions in 2 countries.

Haihong ChenDepartments of Orthopedics and.ORCID 0000-0002-7584-0229
Hao JiDepartments of Orthopedics and.ORCID 0000-0002-8755-3593
Ming ZhangTransplantation, Shanghai Jiao Tong University School of Medicine, Renji Hospital, Shanghai 200127, People's Republic of China.ORCID 0000-0002-6293-0700
Zude LiuDepartments of Orthopedics and.
Lifeng LaoDepartments of Orthopedics and.ORCID 0000-0001-6516-854X
Chao DengDepartments of Orthopedics and.
Jianwei ChenDepartments of Orthopedics and.
Guibin ZhongDepartments of Orthopedics and zhonggb@foxmail.com.ORCID 0000-0003-4990-3465
Fox Valley Orthopedics · USShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeting posttraumatic inflammation is crucial for improving locomotor function. SIRT1 has been shown to play a critical role in disease processes such as hepatic inflammation, rheumatoid arthritis, and acute lung inflammation by regulating inflammation. However, the role of SIRT1 in spinal cord injury (SCI) is unknown. We hypothesized that SIRT1 plays an important role in improving locomotor function after SCI by regulating neuroinflammation. In this study, we investigate the effect of SIRT1 in SCI using pharmacological intervention (SRT1720) and the Mx1-Cre/loxP recombination system to knock out target genes. First, we found that SIRT1 expression at the injured lesion site of wild-type (WT) mice (C57BL/6) decreased 4 h after SCI and lasted for 3 d. Moreover, administration of SRT1720, an agonist of SIRT1, to WT mice significantly improved functional recovery for up to 28 d after injury by reducing the levels of proinflammatory cytokines, the number of M1 macrophages, the number of macrophages/microglia, and the accumulation of perivascular macrophages. In contrast, administration of SRT1720 to SIRT1 knock-out (KO) mice did not improve locomotor recovery or attenuate inflammation. Furthermore, SIRT1 KO mice exhibited worse locomotor recovery, increased levels of inflammatory cytokines, and more M1 macrophages and perivascular macrophages than those of WT mice after SCI. Together, these findings indicate that SRT1720, an SIRT1 agonist, can improve functional recovery by attenuating inflammation after SCI. Therefore, SIRT1 is not only a protective factor but also an anti-inflammatory molecule that exerts beneficial effects on locomotor function after SCI.

Indexed as

AnimalsCell SurvivalFemaleHeterocyclic Compounds, 4 or More RingsLocomotionMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicMyelitisNeuronsNeuroprotective AgentsRecovery of FunctionSirtuin 1Spinal Cord InjuriesHeterocyclic Compounds, 4 or More RingsNeuroprotective AgentsSirt1 protein, mouseSirtuin 1SRT1720inflammatory cytokinesmacrophage/microgliaMx1-creSIRT1spinal cord injurySRT1720

Identifiers

PMID28193684
PMCPMC6596736
OpenAlexW2588609998

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.