Evidence map›Paper›PMID 28409174›Full record

ArticleTranslational perioperative and pain medicine2016

Neurokinin 1 and opioid receptors: relationships and interactions in nervous system.

Jie Xiao, Si Zeng, Xiangrui Wang, Hasan Babazada, Zhanchun Li, Renyu Liu, Weifeng Yu

Open access · diamondAbstract read
In one paragraph

Article in Translational perioperative and pain medicine, 2016. 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
0.5field-weighted citation impact, top 33% 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, 16 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. 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

7 authors at 2 institutions in 2 countries.

Jie XiaoDepartment of Anesthesiology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Si ZengDepartment of Anesthesiology, Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital, Electronic Science and Technology University.
Xiangrui WangDepartment of Anesthesiology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Hasan BabazadaDepartment of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania.
Zhanchun LiDepartment of Anesthesiology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Renyu LiuDepartment of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania.
Weifeng YuDepartment of Anesthesiology, Renji Hospital, School of Medicine, Shanghai Jiaotong University.
Renji Hospital · CNUniversity of Pennsylvania · US

Funding

Water soluble variants of the human mu opioid receptorR01GM111421 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI LIU, RENYU · 2014 to 2018
$1.7M
Structural Approaches for Understanding Opioid and ??-Receptor InteractionsK08GM093115 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI LIU, RENYU · 2010 to 2013
$505k
NIGMS NIH HHS K08 GM093115NIGMS NIH HHS R01 GM111421
6 · The paper itself

Abstract

Opioid receptors and neurokinin 1 receptor (NK1R) are found highly expressed in the central nervous system. The co-localization of these two kinds of receptors suggests that they might interact with each other in both the transmission and modulation of the pain signal. In this review, we explore the relationships between opioid receptors and NK1R. Substance P (SP) plays a modulatory role in the pain transmission by activating the NK1R. Opioid receptor activation can inhibit SP release. NK1R is found participating in the mechanisms of the side effects of the opioids, including opioid analgesic tolerance, hyperalgesia, anxiety behaviors of morphine reward and opioids related respiratory depression. A series of compounds such as NK1R antagonists and ligands works on both mu/delta opioid receptor (MOR/DOR) and NK1R were synthesized as novel analgesics that enhance the clinical pain management efficacy and reduce the dosage and side effects. The current status of these novel ligands and the limitations are discussed in this review. Although the working mechanisms of these ligands remained unclear, they could be used as research tool for developing novel analgesic drugs in the future.

Indexed as

Central nervous systemNeurokinin 1 receptorOpioid receptorsOpioidsSubstance P

Identifiers

PMID28409174
PMCPMC5388438
OpenAlexW2804096679

What OpenQuestion holds

Textmetadata
LicenceTDM
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.