Evidence map›Paper›PMID 30192300›Full record

ArticleNeuroreport2018

Role of receptor-interacting protein 1/receptor-interacting protein 3 in inflammation and necrosis following chronic constriction injury of the sciatic nerve.

Shaofeng Pu, Shuangyue Li, Yongming Xu, Junzhen Wu, Yingying Lv, Dongping Du

Open access · greenAbstract read
In one paragraph

Article in Neuroreport, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.3field-weighted citation impact, top 48% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

6 authors at 2 institutions in 2 countries.

Shaofeng PuDepartment of Pain Management, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai.
Shuangyue LiDepartment of Anesthesiology, Ningbo Urology and Nephrology Hospital, Ningbo, Zhejiang, People's Republic of China.
Yongming XuDepartment of Pain Management, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai.
Junzhen WuDepartment of Pain Management, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai.
Yingying LvDepartment of Pain Management, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai.
Dongping DuDepartment of Pain Management, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai.
Shanghai Jiao Tong University · CNShanghai Sixth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nerve damage often leads to nervous system dysfunction and neuropathic pain. The serine-threonine kinases receptor-interacting protein 1 (RIP1) and 3 (RIP3) are associated with inflammation and cell necrosis. This study aimed to explore the role of RIP1 and RIP3 in sciatic nerve chronic constriction injury (CCI) in mice. On a total of thirty mice, sciatic nerve CCI was performed. The paw withdrawal threshold was measured using Von Frey filaments. The mRNA expression and protein levels of inflammatory factors RIP1 and RIP3 in the dorsal root ganglion (DRG), spinal cord (SC) and hippocampus (HIP) were also determined. We found that paw withdrawal threshold was significantly reduced from the second day after the operation, and the levels of tumour necrosis factor-α and interferon-γ in DRG, SC and HIP were significantly increased on the eighth and 14th days in CCI mice. Furthermore, the downstream signalling molecules of RIP1 and RIP3, GTPase dynamin-related protein-1, NLR family pyrin domain containing-3 (NLRP3) and nuclear factor κB-p65 were upregulated. Increased protein levels of programmed cell death protein 1, which indicate cell death of peripheral and central nervous tissue, were induced by CCI of the sciatic nerve. Overall, this study showed that RIP1 and RIP3 were highly expressed in DRG, SC and HIP of the sciatic nerve in CCI mice and may be involved in chronic neuroinflammation and neuronecrosis.

Indexed as

AnimalsApoptosisCytokinesDisease Models, AnimalGanglia, SpinalGene Expression RegulationGTPase-Activating ProteinsHippocampusInflammationMaleMiceMice, Inbred C57BLNecrosisPain MeasurementReceptor-Interacting Protein Serine-Threonine KinasesRNA, MessengerCytokinesGTPase-Activating ProteinsRalbp1 protein, mouseReceptor-Interacting Protein Serine-Threonine KinasesRipk3 protein, mouseRNA, Messenger

Identifiers

PMID30192300
PMCPMC6181278
OpenAlexW2889678809

What OpenQuestion 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 OpenQuestion graph.