Evidence map›Paper›PMID 36514072›Full record

ArticleJournal of translational medicine2022

Kinin B1 receptor blockade attenuates hepatic fibrosis and portal hypertension in chronic liver diseases in mice.

Dileep Reddy Rampa, Huiying Feng, Sivakumar Allur-Subramaniyan, Kwanseob Shim, Anton Pekcec, Dongwon Lee, Henri Doods, Dongmei Wu

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Inhibition of kinin B1 receptor alleviates SARS-CoV-2-induced long-lasting cardiovascular complications.American journal of physiology. Heart and circulatory physiology · 2025
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Kinins: Locally formed peptides during inflammation with potential use in tissue regeneration.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Article
  9. 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

8 authors at 3 institutions in 3 countries.

Dileep Reddy RampaDepartment of Bio-Nanotechnology and Bio-Convergence Engineering, Jeonbuk National University, Jeonju, South Korea.
Huiying FengDepartment of Bio-Nanotechnology and Bio-Convergence Engineering, Jeonbuk National University, Jeonju, South Korea.
Sivakumar Allur-SubramaniyanDepartment of Animal Biotechnology & Agricultural Convergence Technology, Jeonbuk National University, Jeonju, South Korea.
Kwanseob ShimDepartment of Animal Biotechnology & Agricultural Convergence Technology, Jeonbuk National University, Jeonju, South Korea.
Anton PekcecResearch Beyond Borders, Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach, Germany.
Dongwon LeeDepartment of Bio-Nanotechnology and Bio-Convergence Engineering, Jeonbuk National University, Jeonju, South Korea. dlee@jbnu.ac.kr.
Henri DoodsResearch Beyond Borders, Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach, Germany.
Dongmei WuDepartment of Bio-Nanotechnology and Bio-Convergence Engineering, Jeonbuk National University, Jeonju, South Korea. dongmeiwu18@gmail.com.
Jeonbuk National University · KRBoehringer Ingelheim (Germany) · DEMount Sinai Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsKinin B1 receptors (B1Rs) are implicated in the pathogenesis of fibrosis. This study examined the anti-fibrotic effects of B1R blockade with BI 113823 in two established mouse models of hepatic fibrosis induced by intraperitoneal carbon tetrachloride (CCl

methodsFibrotic liver diseases were induced in mice by intraperitoneal carbon tetrachloride (CCl

resultsB1Rs were strongly induced in fibrotic mouse liver. BI 113823 significantly attenuated liver fibrosis and portal hypertension (PH), and improved survival in both CCl

conclusionsB1Rs merits consideration as a novel therapeutic target for chronic liver fibrosis and PH.

Indexed as

Hypertension, PortalLiver CirrhosisReceptors, PeptideAnimalsCarbon TetrachlorideFibrosisHepatic Stellate CellsHumansKininsLiverMicePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTransforming Growth Factor betaCarbon TetrachlorideKininsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptors, PeptideTransforming Growth Factor betaB1RBI 113823Hepatic fibrosisHepatic inflammationPI3K/AKT signalling pathwayPortal hypertension

Identifiers

PMID36514072
PMCPMC9746183
OpenAlexW4311363268

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.