Evidence map›Paper›PMID 33396223›Full record

ArticleBiology2020

Susceptibility of Asialoglycoprotein Receptor-Deficient Mice to Lps/Galactosamine Liver Injury and Protection by Betaine Administration.

Karuna Rasineni, Serene M L Lee, Benita L McVicker, Natalia A Osna, Carol A Casey, Kusum K Kharbanda

Open access · goldAbstract read
In one paragraph

Article in Biology, 2020. 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
0.6field-weighted citation impact, top 34% 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, 11 citations in OpenAlex.

  1. Review
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  6. Aging · 2023
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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

6 authors at 2 institutions in 1 country.

Karuna RasineniResearch Service, Veterans' Affairs Nebraska-Western Iowa Health Care System, Omaha, NE 68105, USA.
Serene M L LeeDepartment of Internal Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Benita L McVickerResearch Service, Veterans' Affairs Nebraska-Western Iowa Health Care System, Omaha, NE 68105, USA.
Natalia A OsnaResearch Service, Veterans' Affairs Nebraska-Western Iowa Health Care System, Omaha, NE 68105, USA.ORCID 0000-0001-7498-0556
Carol A CaseyResearch Service, Veterans' Affairs Nebraska-Western Iowa Health Care System, Omaha, NE 68105, USA.ORCID 0000-0002-7501-0495
Kusum K KharbandaResearch Service, Veterans' Affairs Nebraska-Western Iowa Health Care System, Omaha, NE 68105, USA.ORCID 0000-0001-7759-8889
VA Nebraska Western Iowa Health Care System · USUniversity of Nebraska Medical Center · US

Funding

Impaired phospholipid methylation results in decreased lipid droplet lipolysis: Role in hepatic steatosisR01AA026723 · NIAAA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI KHARBANDA, KUSUM K. · 2018 to 2022
$1.6M
Pancreas-Adipose-Liver Axis: Role of Ghrelin and Insulin in Alcoholic Fatty LiverK01AA024254 · NIAAA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI RASINENI, KARUNA · 2016 to 2020
$603k
Impaired methylation alters lipid droplet dynamics in liver and adipose tissue: Role in hepatic steatosisI01BX004053 · VA · OMAHA VA MEDICAL CENTER · PI KHARBANDA, KUSUM K. · 2019 to 2023
–
BLRD VA I01 BX001155BLRD VA I01 BX004053NIAAA NIH HHS K01 AA024254NIH HHS R01 AA026723U.S. Department of Veterans Affairs, Biomedical Laboratory Research and Development Service. BX004053
6 · The paper itself

Abstract

backgroundWork from our laboratory has shown that the ethanol-induced increase in apoptotic hepatocellular death is closely related to the impairment in the ability of the asialoglycoprotein receptor (ASGP-R) to remove neighboring apoptotic cells. In this study, we assessed the role of ASGP-R in fulminant liver failure and investigated whether prior treatment with betaine (a naturally occurring tertiary amine) is protective.

methodsLipopolysaccharide (LPS; 50 μg/kg BW) and galactosamine (GalN; 350 mg/kg BW) were injected together to wild-type and ASGP-R-deficient mice that were treated for two weeks prior with or without 2% betaine in drinking water. The mice were sacrificed 1.5, 3, or 4.5 h post-injection, and tissue samples were collected.

resultsLPS/GalN injection generate distinct molecular processes, which includes increased production of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6), thus causing apoptosis as evident by increased caspase-3 activity. ASGP-R deficient animals showed increased liver caspase activities, serum TNF-α and IL-6 levels, as well as more pronounced liver damage compared with the wild-type control animals after intraperitoneal injection of LPS/GalN. In addition, prior administration of betaine was found to significantly attenuate the LPS/GalN-induced increases in liver injury parameters.

conclusionOur work underscores the importance of normal functioning of ASGP-R in preventing severe liver damage and signifies a therapeutic role of betaine in prevention of liver injuries from toxin-induced fulminant liver failure.

Indexed as

apoptosisbetainefulminant liver failuregalactosaminelipopolysaccharide

Identifiers

PMID33396223
PMCPMC7823640
OpenAlexW3114672151

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.