Evidence map›Paper›PMID 24587368›Full record

ArticlePloS one2014

Hemokinin-1(4-11)-induced analgesia selectively up-regulates δ-opioid receptor expression in mice.

Cai-Yun Fu, Rui-Long Xia, Teng-Fei Zhang, Yan Lu, Shi-Fu Zhang, Zhi-Qiang Yu, Tao Jin, Xiao-Zhou Mou

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

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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

8 authors at 4 institutions in 2 countries.

Cai-Yun FuLab of Proteomics and Molecular Enzymology, College of Life Sciences, Zhejiang Sci-Tech University, Hangzhou, China ; Institute for Cell-Based Drug Development of Zhejiang Province, Hangzhou, China.
Rui-Long XiaLab of Proteomics and Molecular Enzymology, College of Life Sciences, Zhejiang Sci-Tech University, Hangzhou, China.
Teng-Fei ZhangLab of Proteomics and Molecular Enzymology, College of Life Sciences, Zhejiang Sci-Tech University, Hangzhou, China.
Yan LuLab of Proteomics and Molecular Enzymology, College of Life Sciences, Zhejiang Sci-Tech University, Hangzhou, China.
Shi-Fu ZhangLab of Proteomics and Molecular Enzymology, College of Life Sciences, Zhejiang Sci-Tech University, Hangzhou, China.
Zhi-Qiang YuCenter for BioEnergetics, The Biodesign Institute, and Department of Chemistry and Biochemistry, Arizona State University, Tempe, Arizona, United States of America.
Tao JinZhejiang Provincial People's Hospital, Hangzhou, China.
Xiao-Zhou MouZhejiang Provincial People's Hospital, Hangzhou, China ; Institute for Cell-Based Drug Development of Zhejiang Province, Hangzhou, China.
Zhejiang Sci-Tech University · CNZhejiang Provincial People's Hospital · CNArizona State University · USZheJiang Institute For Food and Drug Control · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our previous studies have shown that an active fragment of human tachykinins (hHK-1(4-11)) produced an opioid-independent analgesia after intracerebroventricular (i.c.v.) injection in mice, which has been markedly enhanced by a δ OR antagonist, naltrindole hydrochloride (NTI). In this study, we have further characterized the in vivo analgesia after i.c.v. injection of hHK-1(4-11) in mouse model. Our qRT-PCR results showed that the mRNA levels of several ligands and receptors (e.g. PPT-A, PPT-C, KOR, PDYN and PENK) have not changed significantly. Furthermore, neither transcription nor expression of NK1 receptor, MOR and POMC have changed noticeably. In contrast, both mRNA and protein levels of DOR have been up-regulated significantly, indicating that the enhanced expression of δ opioid receptor negatively modulates the analgesia induced by i.c.v. injection of hHK-1(4-11). Additionally, the combinatorial data from our previous and present experiments strongly suggest that the discriminable distribution sites in the central nervous system between hHK-1(4-11) and r/mHK-1 may be attributed to their discriminable analgesic effects. Altogether, our findings will not only contribute to the understanding of the complicated mechanisms regarding the nociceptive modulation of hemokinin-1 as well as its active fragments at supraspinal level, but may also lead to novel pharmacological interventions.

Indexed as

AnalgesiaAnimalsBlotting, WesternFemaleGene ExpressionHumansInjections, IntraventricularMaleMice, Inbred ICRPeptide FragmentsPro-OpiomelanocortinProtein PrecursorsReceptors, Opioid, deltaReceptors, Opioid, muReverse Transcriptase Polymerase Chain ReactionTachykininshemokinin-1Peptide FragmentspreprotachykininPro-OpiomelanocortinProtein PrecursorsReceptors, Opioid, deltaReceptors, Opioid, muTachykinins

Identifiers

PMID24587368
PMCPMC3938741
OpenAlexW1982754935

What OpenQuestion holds

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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.