Evidence map›Paper›PMID 26339646›Full record

ReviewBioMed research international2015

Biological Roles of Resolvins and Related Substances in the Resolution of Pain.

Ji Yeon Lim, Chul-Kyu Park, Sun Wook Hwang

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.4field-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

32 citing papers in PubMed, 54 citations in OpenAlex.

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  16. Role of TRP Channels in Shaping the Gut Microbiome.Pathogens (Basel, Switzerland) · 2020
    Article
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  20. Is TRPA1International journal of molecular sciences · 2019
    Review
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

3 authors at 2 institutions in 1 country.

Ji Yeon LimDepartment of Biomedical Sciences and Department of Physiology, Korea University College of Medicine, Seoul 136-705, Republic of Korea.
Chul-Kyu ParkDepartment of Physiology, Graduate School of Medicine, Gachon University, Incheon 406-799, Republic of Korea.
Sun Wook HwangDepartment of Biomedical Sciences and Department of Physiology, Korea University College of Medicine, Seoul 136-705, Republic of Korea.
Korea University · KRGachon University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endogenous pain-inhibitory substances have rarely been found. A group of powerful pain suppressor molecules that are endogenously generated are now emerging: resolvins and related compounds including neuroprotectins and maresins. These molecules began to be unveiled in a series of inflammation studies more than a decade ago, rapidly shifting the paradigm that explains the mechanism for the inflammatory phase switch. The resolution phase was considered a passive process as proinflammatory mediators disappeared; it is now understood to be actively drawn by the actions of resolvins. Surprisingly, these substances potently affect the pain state. Although this research area is not fully matured, consistently beneficial outcomes have been observed in a various in vivo and in vitro pain models. Furthermore, multiple hypotheses on the neuronal and molecular mechanisms for alleviating pain are being tested, deriving inspiration from existing inflammation and pain studies. This paper serves as a brief summary of the proresolving roles of resolvins and related lipid mediators in inflammation and also as a review for accumulated information of their painkilling actions. This also includes potential receptor-mediated mechanisms and discusses future scientific perspectives. Further diverse approaches will help to construct a hidden axis of natural protection principles and establish proofs of concept for pain relief.

Indexed as

Calcium ChannelsDocosahexaenoic AcidsEicosapentaenoic AcidHumansInflammationInflammation MediatorsNerve Tissue ProteinsPainTransient Receptor Potential ChannelsTRPA1 Cation ChannelTRPV Cation Channels5S,12R,18R-trihydroxy-6Z,8E,10E,14Z,16E-eicosapentaenoic acid7,14-dihydroxydocosa-4,8,10,12,16,19-hexaenoic acidCalcium ChannelsDocosahexaenoic AcidsEicosapentaenoic AcidInflammation MediatorsNerve Tissue Proteinsresolvin D1Transient Receptor Potential ChannelsTRPA1 Cation ChannelTRPA1 protein, humanTRPV1 protein, humanTRPV Cation Channels

Identifiers

PMID26339646
PMCPMC4538417
OpenAlexW1542864268

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.