Evidence map›Paper›PMID 30053799›Full record

ArticleBMC anesthesiology2018

Nefopam downregulates autophagy and c-Jun N-terminal kinase activity in the regulation of neuropathic pain development following spinal nerve ligation.

Seon-Hee Oh, Myung Ha Yoon, Kyung Joon Lim, Byung Sik Yu, In Gook Jee, Ki Tae Jung

Open access · goldAbstract read
In one paragraph

Article in BMC anesthesiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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  8. [Escin alleviates chemotherapy-induced peripheral neuropathic pain by inducing autophagy in the spinal cord of rats].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2020
    Article
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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 1 country.

Seon-Hee OhSchool of Medicine, Chosun University, 309 Pilmundaero, Dong-gu, Gwangju, 501-759, South Korea.
Myung Ha YoonDepartment of Anesthesiology and Pain Medicine, Medical School, Chonnam National University, 42 Jebongro, Donggu, Gwangju, 501-757, South Korea.
Kyung Joon LimDepartment of Anesthesiology and Pain Medicine, School of Medicine, Chosun University, Chosun University Hospital, 365 Pilmun-daero, Dong-gu, Gwangju, 61453, South Korea.
Byung Sik YuDepartment of Anesthesiology and Pain Medicine, School of Medicine, Chosun University, Chosun University Hospital, 365 Pilmun-daero, Dong-gu, Gwangju, 61453, South Korea.
In Gook JeeDepartment of Anesthesiology and Pain Medicine, Chosun University Hospital, 365 Pilmun-daero, Dong-gu, Gwangju, 61453, South Korea.
Ki Tae JungDepartment of Anesthesiology and Pain Medicine, School of Medicine, Chosun University, Chosun University Hospital, 365 Pilmun-daero, Dong-gu, Gwangju, 61453, South Korea. mdmole@chosun.ac.kr.ORCID 0000-0002-2486-9961
Chosun University · KRChonnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeurodegeneration is associated with changes in basal cellular function due to the dysregulation of autophagy. A recent study introduced the involvement of autophagy during spinal nerve ligation (SNL). Nefopam has shown potential for reducing neuropathic pain, but the underlying mechanisms are unknown. Here, we investigated the effects of nefopam on neuropathic pain development following SNL, focusing on the involvement of autophagy.

methodsThe functional role of nefopam in capsaicin-induced autophagy was assessed by human glioblastoma M059 K cells. The neuropathic pain model was used to determine whether the effect of nefopam on pain control was mediated through autophagy control. Neuropathic pain was induced by L5 and L6 SNL in male rats randomized into three groups: Group S (sham-operated), Group C (received normal saline), and Group E (received nefopam). A behavioral test using a von Frey was examined. Expression changes of autophagy in response to nefopam was analyzed in spinal cord tissues (L4-L6) by immunoblotting and immunohistochemistry.

resultsThe paw withdrawal threshold examined on days 3, 5, 7, and 14 post-SNL was significantly higher in Group E than in Group C. SNL increased the levels of microtubule-associated protein 1 light chain 3B (LC3B-1), with concomitant reduction of sequestosome 1 (SQTSM1/p62), compared with Group S, indicating that SNL induced autophagy. These effects were reversed by nefopam injection, and the results were confirmed by immunohistochemistry for LC3-I/II. Furthermore, SNL-mediated JNK activation was markedly decreased following nefopam injection. Hematoxylin and eosin staining on Day 14 post-SNL revealed that SNL caused lymphocyte infiltration and oligodendrocyte localization in the substantia gelatinosa of the dorsal gray horn, which were reduced by nefopam injection.

conclusionCollectively, the mode of action of nefopam on neuropathic pain appears to be associated with downregulation of phospho-JNK and autophagy, as well as modulation of the immune response.

Indexed as

AnimalsAutophagyCapsaicinCell Line, TumorDown-RegulationHumansJNK Mitogen-Activated Protein KinasesLigationLymphocytesMaleMicrotubule-Associated ProteinsNefopamNeuralgiaOligodendrogliaPain MeasurementRatsAnxa3 protein, ratCapsaicinJNK Mitogen-Activated Protein KinasesMicrotubule-Associated ProteinsNefopamSequestosome-1 ProteinSqstm1 protein, ratAutophagyJNKNefopamNeuropathic painRat

Identifiers

PMID30053799
PMCPMC6064146
OpenAlexW2883683061

What OpenQuestion holds

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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.