Evidence map›Paper›PMID 34220535›Full record

ArticleFrontiers in physiology2021

Melatonin Attenuates Intervertebral Disk Degeneration

Xiexing Wu, Yijie Liu, Jiacheng Du, Xiaoping Li, Jiayi Lin, Li Ni, Pengfei Zhu, Hong Zhou, Fanchen Kong, Huilin Yang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

8 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Recent Advances in Managing Spinal Intervertebral Discs Degeneration.International journal of molecular sciences · 2022
    Review
  8. 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

12 authors at 3 institutions in 1 country.

Xiexing WuDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Yijie LiuDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Jiacheng DuDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Xiaoping LiDepartment of Clinical Education, The First Affiliated Hospital of Soochow University, Suzhou, China.
Jiayi LinDepartment of Orthopedics Center, Ningbo No. 2 Hospital, Ningbo, China.
Li NiDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Pengfei ZhuDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Hong ZhouDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Fanchen KongDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Huilin YangDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Dechun GengDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Haiqing MaoDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
First Affiliated Hospital of Soochow University · CNSoochow University · CNNingbo No. 2 Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of this study is to verify whether melatonin (Mel) could mitigate intervertebral disk degeneration (IVDD) in rats and to investigate the potential mechanism of it.

methodA rat acupuncture model of IVDD was established with intraperitoneal injection of Mel. The effect of Mel on IVDD was analyzed

resultsThe percent disk height index (%DHI) and MRI signal decreased after initial puncture in the degeneration group compared with the control group, while Mel treatment protected disk height from decline and prevented the loss of water during the degeneration process. In the meantime, the histological staining of the Mel groups showed more integrity and well-ordered construction of the NP and EPs in both low and high concentration than that of the degeneration group. In addition, more deep-brown staining of type II collagen (Coll-II) was shown in the Mel groups compared with the degeneration group. Furthermore, in rat samples, immunohistochemical staining showed more positive cells of Mel receptors 1a and 1b in the EPs, instead of in the NP. Moreover, evident osteochondral lacuna formation was observed in rat EPs in the degeneration group; after Mel treatment, the osteochondral destruction alleviated accompanying fewer receptor activator for nuclear factor-κB ligand (RANKL) and tartrate-resistant acid phosphatase (TRAP)-stained positive cells expressed in the EPs.

conclusionThese results indicate that Mel protects the integrity of the EPs and attenuates IVDD by binding to the Mel receptors in the EPs. It may alleviate the inflammatory response and matrix degradation of EPCs activated by NF-κB pathway.

Indexed as

cartilaginous endplatesinflammationintervertebral disk degenerationmatrix degradationmelatoninNF-κBosteoclastogenesis

Identifiers

PMID34220535
PMCPMC8248798
OpenAlexW3173121220

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.