Evidence map›Paper›PMID 29895352›Full record

ArticleGene expression2018

Direct Comparison of the Thioacetamide and Azoxymethane Models of Type A Hepatic Encephalopathy in Mice.

Stephanie Grant, Matthew McMillin, Gabriel Frampton, Anca D Petrescu, Elaina Williams, Victoria Jaeger, Jessica Kain, Sharon DeMorrow

Open access · greenAbstract readComparative Study
In one paragraph

Article in Gene expression, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.7field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 42 citations in OpenAlex.

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  16. The neurogliovascular unit in hepatic encephalopathy.JHEP reports : innovation in hepatology · 2021
    Review
  17. Article
  18. 2021 ISHEN guidelines on animal models of hepatic encephalopathy.Liver international : official journal of the International Association for the Study of the Liver · 2021
    Review
  19. Review
  20. 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 2 institutions in 1 country.

Stephanie GrantDepartment of Medical Physiology, Texas A&M Health Science Center College of Medicine, Temple, TX, USA.
Matthew McMillinCentral Texas Veterans Healthcare System, Temple, TX, USA.
Gabriel FramptonDepartment of Medical Physiology, Texas A&M Health Science Center College of Medicine, Temple, TX, USA.
Anca D PetrescuDepartment of Medical Physiology, Texas A&M Health Science Center College of Medicine, Temple, TX, USA.
Elaina WilliamsDepartment of Medical Physiology, Texas A&M Health Science Center College of Medicine, Temple, TX, USA.
Victoria JaegerDepartment of Medical Physiology, Texas A&M Health Science Center College of Medicine, Temple, TX, USA.
Jessica KainDepartment of Medical Physiology, Texas A&M Health Science Center College of Medicine, Temple, TX, USA.
Sharon DeMorrowDepartment of Medical Physiology, Texas A&M Health Science Center College of Medicine, Temple, TX, USA.
Texas A&M Health Science Center · USCentral Texas Veterans Health Care System · US

Funding

Dysregulation of hypothalamic neuropeptides is associated with biliary hyperplasiaR01DK082435 · NIDDK · UNIVERSITY OF TEXAS AT AUSTIN · PI DEMORROW, SHARON · 2010 to 2020
$2.7M
Molecular mechanisms of drug-induced liver injuryR01DK112803 · NIDDK · UNIVERSITY OF TEXAS AT AUSTIN · PI DEMORROW, SHARON · 2018 to 2021
$1.4M
The role of hypothalamic neuropeptides on biliary function during cholestasisI01BX002638 · VA · OLIN TEAGUE VETERANS CENTER · PI DEMORROW, SHARON · 2015 to 2018
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Pathogenic role of thrombospondin-1 in acute and chronic liver failureIK2BX003486 · VA · OLIN TEAGUE VETERANS CENTER · PI MCMILLIN, MATTHEW · 2017 to 2022
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BLRD VA I01 BX002638BLRD VA IK2 BX003486NIDDK NIH HHS R01 DK082435NIDDK NIH HHS R01 DK112803
6 · The paper itself

Abstract

Acute liver failure is a devastating consequence of hepatotoxic liver injury that can lead to the development of hepatic encephalopathy. There is no consensus on the best model to represent these syndromes in mice, and therefore the aim of this study was to classify hepatic and neurological consequences of azoxymethane- and thioacetamide-induced liver injury. Azoxymethane-treated mice were euthanized at time points representing absence of minor and significant stages of neurological decline. Thioacetamide-treated mice had tissue collected at up to 3 days following daily injections. Liver histology, serum chemistry, bile acids, and cytokine levels were measured. Reflexes, grip strength measurement, and ataxia were calculated for all groups. Brain ammonia, bile acid levels, cerebral edema, and neuroinflammation were measured. Finally, in vitro and in vivo assessments of blood-brain barrier function were performed. Serum transaminases and liver histology demonstrate that both models generated hepatotoxic liver injury. Serum proinflammatory cytokine levels were significantly elevated in both models. Azoxymethane-treated mice had progressive neurological deficits, while thioacetamide-treated mice had inconsistent neurological deficits. Bile acids and cerebral edema were increased to a higher degree in azoxymethane-treated mice, while cerebral ammonia and neuroinflammation were greater in thioacetamide-treated mice. Blood-brain barrier permeability exists in both models but was likely not due to direct toxicity of azoxymethane or thioacetamide on brain endothelial cells. In conclusion, both models generate acute liver injury and hepatic encephalopathy, but the requirement of a single injection and the more consistent neurological decline make azoxymethane treatment a better model for acute liver failure with hepatic encephalopathy.

Indexed as

Disease Models, AnimalAnimalsAzoxymethaneBiomarkersBrainHepatic EncephalopathyLiverMaleMiceMice, Inbred C57BLThioacetamideAzoxymethaneBiomarkersThioacetamide

Identifiers

PMID29895352
PMCPMC6190119
OpenAlexW2808591612

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.