Evidence map›Paper›PMID 26573293›Full record

ArticleGut and liver2016

Doxazosin Treatment Attenuates Carbon Tetrachloride-Induced Liver Fibrosis in Hamsters through a Decrease in Transforming Growth Factor β Secretion.

Martin Humberto Muñoz-Ortega, Raúl Wiliberto Llamas-Ramírez, Norma Isabel Romero-Delgadillo, Tania Guadalupe Elías-Flores, Edgar de Jesus Tavares-Rodríguez, María Del Rosario Campos-Esparza, Daniel Cervantes-García, Luis Muñoz-Fernández, Martin Gerardo-Rodríguez, Javier Ventura-Juárez

Open access · diamondAbstract read
In one paragraph

Article in Gut and liver, 2016. 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
1.0field-weighted citation impact, top 24% 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, 20 citations in OpenAlex.

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  8. Curcumin andJournal of immunology research · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 2 countries.

Martin Humberto Muñoz-OrtegaDepartment of Chemistry, Center of Basic Sciences, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Raúl Wiliberto Llamas-RamírezDepartment of Morphology, Center of Basic Sciences, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Norma Isabel Romero-DelgadilloDepartment of Morphology, Center of Basic Sciences, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Tania Guadalupe Elías-FloresDepartment of Morphology, Center of Basic Sciences, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Edgar de Jesus Tavares-RodríguezDepartment of Morphology, Center of Basic Sciences, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
María Del Rosario Campos-EsparzaDepartment of Morphology, Center of Basic Sciences, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Daniel Cervantes-GarcíaDepartment of Chemistry, Center of Basic Sciences, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Luis Muñoz-FernándezDepartment of Pathology, Centenary Hospital Miguel Hidalgo, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Martin Gerardo-RodríguezDepartment of Physiology, Center of Basic Sciences, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Javier Ventura-JuárezDepartment of Morphology, Center of Basic Sciences, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Autonomous University of Aguascalientes · MXDivision of Chemistry · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsThe development of therapeutic strategies for the treatment of cirrhosis has become an important focus for basic and clinical researchers. Adrenergic receptor antagonists have been evaluated as antifibrotic drugs in rodent models of carbon tetrachloride (CCl4)-induced cirrhosis. The aim of the present study was to evaluate the effects of carvedilol and doxazosin on fibrosis/cirrhosis in a hamster animal model.

methodsCirrhotic-induced hamsters were treated by daily administration of carvedilol and doxazosin for 6 weeks. Hepatic function and histological evaluation were conducted by measuring biochemical markers, including total bilirubin, aspartate aminotransferase, alanine aminotransferase and albumin, and liver tissue slices. Additionally, transforming growth factor β (TGF-β) immunohistochemistry was analyzed.

resultsBiochemical markers revealed that hepatic function was restored after treatment with doxazosin and carvedilol. Histological evaluation showed a decrease in collagen type I deposits and TGF-β-secreting cells.

conclusionsTaken together, these results suggest that the decrease in collagen type I following treatment with doxazosin or carvedilol is achieved by decreasing the profibrotic activities of TGF-β via the blockage of α1- and β-adrenergic receptor. Consequently, a diminution of fibrotic tissue in the CCl4-induced model of cirrhosis is achieved.

Indexed as

Adrenergic alpha-1 Receptor AntagonistsAlanine TransaminaseAnimalsAspartate AminotransferasesBilirubinCarbazolesCarbon TetrachlorideCarvedilolCollagen Type ICricetinaeDoxazosinLiverLiver CirrhosisLiver Function TestsPropanolaminesSerum AlbuminAdrenergic alpha-1 Receptor AntagonistsAlanine TransaminaseAspartate AminotransferasesBilirubinCarbazolesCarbon TetrachlorideCarvedilolCollagen Type IDoxazosinPropanolaminesSerum AlbuminTransforming Growth Factor betaAdrenergic pathwayAdrenergic receptor antagonistCirrhosisCollagenTransforming growth factor beta

Identifiers

PMID26573293
PMCPMC4694741
OpenAlexW2322395094

What OpenQuestion holds

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LicenceCC BY-NC
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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.