Evidence map›Paper›PMID 29542680›Full record

ReviewActa pharmacologica Sinica2018

Phoenixin: a novel brain-gut-skin peptide with multiple bioactivity.

Rong-Ming Lyu, Alan Cowan, Ying Zhang, Yi-Hung Chen, Siok L Dun, Jaw-Kang Chang, Nae J Dun, Jin Jun Luo

Open access · bronzeAbstract readReview
In one paragraph

Review in Acta pharmacologica Sinica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Regulation and physiological functions of phoenixin.Frontiers in molecular biosciences · 2022
    Review
  7. Article
  8. The protective effects of phoenixin-14 against lipopolysaccharide-induced inflammation and inflammasome activation in astrocytes.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2020
    Article
  9. Phoenixin-20 suppresses food intake, modulates glucoregulatory enzymes, and enhances glycolysis in zebrafish.American journal of physiology. Regulatory, integrative and comparative physiology · 2020
    Article
  10. 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

8 authors at 5 institutions in 3 countries.

Rong-Ming LyuPhoenix Pharmaceuticals Inc, Burlingame, CA 94010, USA.
Alan CowanCenter for Substance Abuse Research, Lewis Katz School of Medicine, Temple University, Philadelphia, PA 19140, USA.
Ying ZhangDepartment of Pharmacology, Lewis Katz School of Medicine, Temple University, Philadelphia, PA 19140, USA.
Yi-Hung ChenGraduate Institute of Acupuncture Science, China Medical University, Taichung, Taiwan, China.
Siok L DunDepartment of Pharmacology, Lewis Katz School of Medicine, Temple University, Philadelphia, PA 19140, USA.
Jaw-Kang ChangPhoenix Pharmaceuticals Inc, Burlingame, CA 94010, USA.
Nae J DunDepartment of Pharmacology, Lewis Katz School of Medicine, Temple University, Philadelphia, PA 19140, USA.
Jin Jun LuoDepartment of Pharmacology, Lewis Katz School of Medicine, Temple University, Philadelphia, PA 19140, USA.
Temple University · USAcceleron Pharma (United States) · USChina Medical University · TWCollaborative Drug Discovery (United States) · USKunming Medical University · CN

Funding

Pilot Projects Core (PPC)P30DA013429 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI Anjali M Rajadhyaksha · 2000 to 2026
$34.6M
NIDA NIH HHS P30 DA013429
6 · The paper itself

Abstract

In this brief review we summarize the current fndings relative to the discovery of a small peptide ligand, phoenixin (PNX). Using a bioinformatic approach, two novel peptides PNX-14 and PNX-20 containing 14 and 20 amino acids, respectively, were isolated from diverse tissues including the brain, heart, lung and stomach. Mass spectrometry analysis identified a major and minor peak corresponding to PNX-14 and PNX-20, in rat or mouse spinal cord extracts. With the use of a rabbit polyclonal antiserum, phoenixin immunoreactivity (irPNX) was detected in discrete areas of the rodent brain including several hypothalamic subnuclei and dorsal motor nucleus of the vagus. In addition, irPNX was detected in a population of sensory ganglion cells including dorsal root ganglion, nodose ganglion and trigeminal ganglion, and in cell processes densely distributed to the superficial layers of the dorsal horn, nucleus of the solitary tract and spinal trigeminal tract. irPNX cell processes were also detected in the skin and myenteric plexus, suggesting a brain-gut and/or brain-skin connection. Pharmacological studies show that PNX-14 injected subcutaneously to the nape of the neck of mice provoked dose-dependent repetitive scratching bouts directed to the back of the neck with the hindpaws. Our result suggests that the peptide PNX-14 and/or PNX-20, may serve as one of the endogenous signal molecules transducing itch sensation. Additionally, results from other laboratories show that exogenous PNX may affect a number of diverse behaviors such as memory formation, depression, reproduction, food-intake and anxiolytic-like behaviors.

Indexed as

Hypothalamic HormonesPeptide HormonesPeptidesAmino Acid SequenceAnimalsHumansHypothalamusMembrane ProteinsMemoryMitochondrial ProteinsMyenteric PlexusPruritusSpinal CordHypothalamic HormonesMembrane ProteinsMitochondrial ProteinsPeptide HormonesPeptidesphoenixinSmim20 protein, mouseSmim20 protein, rat

Identifiers

PMID29542680
PMCPMC5943905
OpenAlexW2790359783

What OpenQuestion holds

Textmetadata
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.