Evidence map›Paper›PMID 31350433›Full record

ArticleScientific reports2019

BAM8-22 and its receptor MRGPRX1 may attribute to cholestatic pruritus.

Babina Sanjel, Han-Joo Maeng, Won-Sik Shim

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Endosomal MrGPRX1 signaling sensitizes TRPV1 to enhance itch.Frontiers in molecular neuroscience · 2026
    Article
  4. Article
  5. Article
  6. Glucosylsphingosine evokes pruritus via activation of 5-HTBritish journal of pharmacology · 2022
    Article
  7. Review
  8. Peripheral Mechanisms of Itch.The Journal of investigative dermatology · 2022
    Review
  9. Frontiers in molecular neuroscience · 2022
    Review
  10. MRGPRX4 in Cholestatic Pruritus.Seminars in liver disease · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Emerging Therapeutic Options for Chronic Pruritus.American journal of clinical dermatology · 2020
    Review
  15. 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 1 institution in 1 country.

Babina SanjelCollege of Pharmacy, Gachon University, Hambakmoero 191, Yeonsu-gu, Incheon, 21936, Republic of Korea.
Han-Joo MaengCollege of Pharmacy, Gachon University, Hambakmoero 191, Yeonsu-gu, Incheon, 21936, Republic of Korea.
Won-Sik ShimCollege of Pharmacy, Gachon University, Hambakmoero 191, Yeonsu-gu, Incheon, 21936, Republic of Korea. wsshim@gachon.ac.kr.ORCID http://orcid.org/0000-0002-1020-685X
Gachon University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pruritus is an unexpected symptom observed in cholestasis and its mechanism is still unclear. Here, we show that bovine adrenal medulla (BAM) 8-22, an endogenous itch-inducing peptide, could be involved in cholestatic pruritus. It was found that bile duct ligation (BDL) mice, an obstructive cholestasis model, showed increased spontaneous scratching behaviour. Importantly, the mRNA level of proenkephalin, a precursor polypeptide of BAM8-22, was significantly increased in the skin of BDL mice. Furthermore, the mRNA level of Mrgprx1, which encodes a receptor for BAM8-22, was significantly increased in the dorsal root ganglia (DRG) of BDL mice. This was further confirmed by elevation of intracellular calcium levels upon BAM8-22 treatment in primarily-cultured DRG neurons. In addition, BDL mice showed augmented scratching behaviour by BAM8-22, indicating enhanced activity of MRGPRX1. Moreover, the skin homogenate of BDL mice induced elevation of intracellular calcium levels through MRGPRX1. Finally, among the various bile acids, chenodeoxycholic acid significantly increased proenkephalin transcription in a human keratinocyte cell line (HaCaT). In conclusion, cholestatic pruritus could be attributed in part to enhanced action of both BAM8-22 in the skin and its receptor MRGPRX1 in sensory neurons.

Indexed as

AnimalsBehavior, AnimalBile DuctsCattleCell LineCholestasisEnkephalinsGanglia, SpinalHumansKeratinocytesMaleMiceMice, Inbred ICRPeptide FragmentsProtein PrecursorsPruritusbovine adrenal medulla 8-22EnkephalinsMrgprx2 protein, mousePeptide FragmentsproenkephalinProtein PrecursorsReceptors, G-Protein-Coupled

Identifiers

PMID31350433
PMCPMC6659683
OpenAlexW2966834148

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.