A critical review of histopathological findings associated with endocrine and non-endocrine hepatic toxicity in fish models

Although frequently examined as a target organ for non-endocrine toxicity, histopathological evaluation of the liver is becoming a routine component of endocrine disruption studies that utilize various fish species as test subjects. However, the interpretation of microscopic liver findings can be ch...

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Published inAquatic toxicology Vol. 197; pp. 60 - 78
Main Authors Wolf, Jeffrey C., Wheeler, James R.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.04.2018
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Abstract Although frequently examined as a target organ for non-endocrine toxicity, histopathological evaluation of the liver is becoming a routine component of endocrine disruption studies that utilize various fish species as test subjects. However, the interpretation of microscopic liver findings can be challenging, especially when attempting to distinguish adverse changes associated with endocrine disrupting substances from those caused by systemic or direct hepatic toxicity. The purpose of this project was to conduct a critical assessment of the available peer-reviewed and grey literature concerning the histopathologic effects of reproductive endocrine active substances (EAS) and non-endocrine acting substances in the livers of fish models, and to determine if liver histopathology can be used to reliably distinguish endocrine from non-endocrine etiologies. The results of this review suggest that few compound-specific histopathologic liver effects have been identified, among which are estrogen agonist-induced increases in hepatocyte basophilia and proteinaceous intravascular fluid in adult male teleosts, and potentially, decreased hepatocyte basophilia in female fish exposed to substances that possess androgenic, anti-estrogenic, or aromatase inhibitory activity. This review also used published standardized methodology to assess the credibility of the histopathology data in each of the 117 articles that reported liver effects of treatment, and consequently it was determined that in only 37% of those papers were the data considered either highly credible or credible. The outcome of this work highlights the value of histopathologic liver evaluation as an investigative tool for EAS studies, and provides information that may have implications for EAS hazard assessment.
AbstractList Although frequently examined as a target organ for non-endocrine toxicity, histopathological evaluation of the liver is becoming a routine component of endocrine disruption studies that utilize various fish species as test subjects. However, the interpretation of microscopic liver findings can be challenging, especially when attempting to distinguish adverse changes associated with endocrine disrupting substances from those caused by systemic or direct hepatic toxicity. The purpose of this project was to conduct a critical assessment of the available peer-reviewed and grey literature concerning the histopathologic effects of reproductive endocrine active substances (EAS) and non-endocrine acting substances in the livers of fish models, and to determine if liver histopathology can be used to reliably distinguish endocrine from non-endocrine etiologies. The results of this review suggest that few compound-specific histopathologic liver effects have been identified, among which are estrogen agonist-induced increases in hepatocyte basophilia and proteinaceous intravascular fluid in adult male teleosts, and potentially, decreased hepatocyte basophilia in female fish exposed to substances that possess androgenic, anti-estrogenic, or aromatase inhibitory activity. This review also used published standardized methodology to assess the credibility of the histopathology data in each of the 117 articles that reported liver effects of treatment, and consequently it was determined that in only 37% of those papers were the data considered either highly credible or credible. The outcome of this work highlights the value of histopathologic liver evaluation as an investigative tool for EAS studies, and provides information that may have implications for EAS hazard assessment.
Although frequently examined as a target organ for non-endocrine toxicity, histopathological evaluation of the liver is becoming a routine component of endocrine disruption studies that utilize various fish species as test subjects. However, the interpretation of microscopic liver findings can be challenging, especially when attempting to distinguish adverse changes associated with endocrine disrupting substances from those caused by systemic or direct hepatic toxicity. The purpose of this project was to conduct a critical assessment of the available peer-reviewed and grey literature concerning the histopathologic effects of reproductive endocrine active substances (EAS) and non-endocrine acting substances in the livers of fish models, and to determine if liver histopathology can be used to reliably distinguish endocrine from non-endocrine etiologies. The results of this review suggest that few compound-specific histopathologic liver effects have been identified, among which are estrogen agonist-induced increases in hepatocyte basophilia and proteinaceous intravascular fluid in adult male teleosts, and potentially, decreased hepatocyte basophilia in female fish exposed to substances that possess androgenic, anti-estrogenic, or aromatase inhibitory activity. This review also used published standardized methodology to assess the credibility of the histopathology data in each of the 117 articles that reported liver effects of treatment, and consequently it was determined that in only 37% of those papers were the data considered either highly credible or credible. The outcome of this work highlights the value of histopathologic liver evaluation as an investigative tool for EAS studies, and provides information that may have implications for EAS hazard assessment.Although frequently examined as a target organ for non-endocrine toxicity, histopathological evaluation of the liver is becoming a routine component of endocrine disruption studies that utilize various fish species as test subjects. However, the interpretation of microscopic liver findings can be challenging, especially when attempting to distinguish adverse changes associated with endocrine disrupting substances from those caused by systemic or direct hepatic toxicity. The purpose of this project was to conduct a critical assessment of the available peer-reviewed and grey literature concerning the histopathologic effects of reproductive endocrine active substances (EAS) and non-endocrine acting substances in the livers of fish models, and to determine if liver histopathology can be used to reliably distinguish endocrine from non-endocrine etiologies. The results of this review suggest that few compound-specific histopathologic liver effects have been identified, among which are estrogen agonist-induced increases in hepatocyte basophilia and proteinaceous intravascular fluid in adult male teleosts, and potentially, decreased hepatocyte basophilia in female fish exposed to substances that possess androgenic, anti-estrogenic, or aromatase inhibitory activity. This review also used published standardized methodology to assess the credibility of the histopathology data in each of the 117 articles that reported liver effects of treatment, and consequently it was determined that in only 37% of those papers were the data considered either highly credible or credible. The outcome of this work highlights the value of histopathologic liver evaluation as an investigative tool for EAS studies, and provides information that may have implications for EAS hazard assessment.
Author Wolf, Jeffrey C.
Wheeler, James R.
Author_xml – sequence: 1
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/29448125$$D View this record in MEDLINE/PubMed
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Tue Jul 01 02:26:30 EDT 2025
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IsDoiOpenAccess true
IsOpenAccess true
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IsScholarly true
Keywords DMN
MEOGRT
Liver
MDHT
TCDD
Vtg
Endocrine disruption
DEN
Histopathology
Data credibility
EAS
PAH
Fish
HC
MTC
Hepatotoxicity
MOA
Language English
License This is an open access article under the CC BY-NC-ND license.
Copyright © 2018 The Author(s). Published by Elsevier B.V. All rights reserved.
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MergedId FETCHMERGED-LOGICAL-c445t-b0356996be53cb2bd2ec44b35393c64dfc096af85120adf08b9bad813e14e5b3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
OpenAccessLink https://www.sciencedirect.com/science/article/pii/S0166445X18300201
PMID 29448125
PQID 2003037876
PQPubID 23479
PageCount 19
ParticipantIDs proquest_miscellaneous_2045829036
proquest_miscellaneous_2003037876
pubmed_primary_29448125
crossref_primary_10_1016_j_aquatox_2018_01_013
crossref_citationtrail_10_1016_j_aquatox_2018_01_013
elsevier_sciencedirect_doi_10_1016_j_aquatox_2018_01_013
ProviderPackageCode CITATION
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PublicationCentury 2000
PublicationDate April 2018
2018-04-00
2018-Apr
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PublicationDateYYYYMMDD 2018-04-01
PublicationDate_xml – month: 04
  year: 2018
  text: April 2018
PublicationDecade 2010
PublicationPlace Netherlands
PublicationPlace_xml – name: Netherlands
PublicationTitle Aquatic toxicology
PublicationTitleAlternate Aquat Toxicol
PublicationYear 2018
Publisher Elsevier B.V
Publisher_xml – name: Elsevier B.V
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Snippet Although frequently examined as a target organ for non-endocrine toxicity, histopathological evaluation of the liver is becoming a routine component of...
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SubjectTerms active ingredients
adults
Androgens - toxicity
Animals
aromatase
Data credibility
Endocrine disruption
Endocrine Disruptors - toxicity
enzyme inhibition
estrogens
Estrogens - toxicity
females
Fish
Fishes - metabolism
hazard characterization
Hepatotoxicity
Histopathology
Liver
Liver - drug effects
Liver - pathology
males
toxicity
Water Pollutants, Chemical - toxicity
Title A critical review of histopathological findings associated with endocrine and non-endocrine hepatic toxicity in fish models
URI https://dx.doi.org/10.1016/j.aquatox.2018.01.013
https://www.ncbi.nlm.nih.gov/pubmed/29448125
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https://www.proquest.com/docview/2045829036
Volume 197
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