Evidence map›Paper›PMID 20071245›Full record

ArticleThe journal of pain2010

Endothelin-A receptor antagonism attenuates carcinoma-induced pain through opioids in mice.

Phuong N Quang, Brian L Schmidt

Abstract read
In one paragraph

Article in The journal of pain, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 43 citations in OpenAlex.

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  15. Article
  16. New perspectives on the endothelin axis in pain.Pharmacological research · 2011
    Review
  17. Orofacial pain.Pain · 2011
    Review
  18. Article
  19. Mechanism of cancer pain.Molecular interventions · 2010
    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

2 authors at 1 institution in 1 country.

Phuong N QuangUCSF School of Dentistry, Oral and Craniofacial Sciences Graduate Program, University of California, San Francisco, San Francisco, CA 94143-0440, USA.
Brian L Schmidt
University of California, San Francisco · US

Funding

A Novel Gnawing Assay to Quantify Nociception in Models of Chronic Orofacial PainR21DE018561 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SCHMIDT, BRIAN L · 2007 to 2008
$422k
NIDCR NIH HHS R21 DE018561
6 · The paper itself

Abstract

unlabelledWe previously reported that endothelin A (ET-A) receptor antagonism attenuates carcinoma-induced pain in a cancer pain mouse model. In this study, we investigated the mechanism of ET-A receptor-mediated antinociception and evaluated the role of endogenous opioid analgesia. Squamous cell carcinoma (SCC) cell culture treated with the ET-A receptor antagonist (BQ-123) at 10(-6) M and 10(-5) M significantly increased production and secretion of beta-endorphin and leu-enkephalin, respectively. Behavioral studies were performed by inducing tumors in the hind paw of female nude mice with local injection of cells derived from a human oral SCC. Significant pain, as indicated by reduction in withdrawal thresholds in response to mechanical stimulation, began at 4 days after SCC inoculation and lasted to 18 days, the last day of measurement. Local administration of either naloxone methiodide (500 microg/kg), selective antagonists for mu-opioid receptor (CTOP, 500 microg/kg), or delta-opioid receptor (naltrindole, 11 mg/kg) but not kappa-opioid receptor (nor-BNI, 2.5 mg/kg) significantly reversed antinociception observed from ET-A receptor antagonism (BQ-123, 92 mg/kg) in cancer animals. These results demonstrate that antagonism of peripheral ET-A receptor attenuates carcinoma pain by modulating release of endogenous opioids to act on opioid receptors in the cancer microenvironment. PERSPECTIVE: This article proposes a novel mechanism for ET-A receptor antagonist drugs in managing cancer-induced pain. An improved understanding of the role of innate opioid analgesia in ET-A receptor-mediated antinociception might provide novel alternatives to morphine therapy for the treatment of cancer pain.

Indexed as

Endothelin A Receptor AntagonistsAnalgesicsAnimalsAntihypertensive AgentsCarcinoma, Squamous CellCells, CulturedDisease Models, AnimalFemaleHumansIntractable PainMiceMice, NudeNarcotic AntagonistsNeoplasms, ExperimentalNeoplasm TransplantationOpioid PeptidesAnalgesicsAntihypertensive Agentscyclo(Trp-Asp-Pro-Val-Leu)Endothelin A Receptor AntagonistsNarcotic AntagonistsOpioid PeptidesPeptides, CyclicReceptors, Opioid

Identifiers

PMID20071245
PMCPMC2891170
OpenAlexW2118369266

What OpenQuestion holds

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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.