Serveur d'exploration sur l'esturgeon

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Is hepatic oxidative stress a main driver of dietary selenium toxicity in white sturgeon (Acipenser transmontanus)?

Identifieur interne : 000053 ( Main/Merge ); précédent : 000052; suivant : 000054

Is hepatic oxidative stress a main driver of dietary selenium toxicity in white sturgeon (Acipenser transmontanus)?

Auteurs : Jenna Zee [Canada] ; Sarah Patterson [Canada] ; Steve Wiseman [Canada] ; Markus Hecker [Canada]

Source :

RBID : pubmed:27494256

English descriptors

Abstract

Most species of sturgeon have experienced significant population declines and poor recruitment over the past decades, leading many, including white sturgeon (Acipenser transmontanus), to be listed as endangered. Reasons for these declines are not yet fully understood but benthic lifestyle, longevity, and delayed sexual maturation likely render sturgeon particularly susceptible to factors such as habitat alteration and contaminant exposures. One contaminant of particular concern to white sturgeon is selenium (Se), especially in its more bioavailable form selenomethionine (SeMet), as it is known to efficiently bioaccumulate in prey items of this species. Studies have shown white sturgeon to be among the most sensitive species of fish to dietary SeMet as well as other pollutants such as metals, dioxin-like chemicals and endocrine disrupters. One of the primary hypothesized mechanisms of toxicity of SeMet in fish is oxidative stress; however, little is know about the specific mode by which SeMet affects the health of white sturgeon. Therefore, the aim of this study was to characterize oxidative stress and associated antioxidant responses as a molecular event of toxicity, and to link it with the pathological effects observed previously. Specifically, three-year-old white sturgeon were exposed for 72 days via their diet to 1.4, 5.6, 22.4 or 104.4µg Se per g feed (dm). Doses were chosen to range over a necessary Se intake level, current environmentally relevant intakes and an intake representing predicted increases of Se release. Lipid hydroperoxides, which are end products of lipid oxidation, were quantified as a marker of oxidative stress. Changes in gene expression of glutathione peroxidase (GPx), superoxide dismutase, catalase, glutathione S-transferase, apoptosis inducing factor and caspase 3 were quantified as markers of the response to oxidative stress. Concentrations of lipid hydroperoxides were highly variable within dose groups and no dose response was observed. GPx expression was significantly increased in the low dose group indicating an induced antioxidant response. Expression of other genes were not significantly induced or suppressed. Overall, there was very little evidence of oxidative stress, and therefore, in contrast to previous reports on other species of teleost fishes, oxidative stress is not believed to be a main driver of toxicity in white sturgeon exposed to SeMet.

DOI: 10.1016/j.ecoenv.2016.07.004
PubMed: 27494256

Links toward previous steps (curation, corpus...)


Links to Exploration step

pubmed:27494256

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Is hepatic oxidative stress a main driver of dietary selenium toxicity in white sturgeon (Acipenser transmontanus)?</title>
<author>
<name sortKey="Zee, Jenna" sort="Zee, Jenna" uniqKey="Zee J" first="Jenna" last="Zee">Jenna Zee</name>
<affiliation wicri:level="1">
<nlm:affiliation>School of Environment and Sustainability, University of Saskatchewan, Room 323, Kirk Hall, 117 Science Place, Saskatoon, Saskatchewan, Canada S7N 5C8. Electronic address: jmz584@mail.usask.ca.</nlm:affiliation>
<country>Canada</country>
<wicri:regionArea>School of Environment and Sustainability, University of Saskatchewan, Room 323, Kirk Hall, 117 Science Place, Saskatoon, Saskatchewan</wicri:regionArea>
<wicri:noRegion>Saskatchewan</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Patterson, Sarah" sort="Patterson, Sarah" uniqKey="Patterson S" first="Sarah" last="Patterson">Sarah Patterson</name>
<affiliation wicri:level="1">
<nlm:affiliation>Toxicology Centre, University of Saskatchewan, 44 Campus Drive, Saskatoon, Saskatchewan, Canada S7N 5B3. Electronic address: sep662@mail.usask.ca.</nlm:affiliation>
<country>Canada</country>
<wicri:regionArea>Toxicology Centre, University of Saskatchewan, 44 Campus Drive, Saskatoon, Saskatchewan</wicri:regionArea>
<wicri:noRegion>Saskatchewan</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Wiseman, Steve" sort="Wiseman, Steve" uniqKey="Wiseman S" first="Steve" last="Wiseman">Steve Wiseman</name>
<affiliation wicri:level="1">
<nlm:affiliation>Toxicology Centre, University of Saskatchewan, 44 Campus Drive, Saskatoon, Saskatchewan, Canada S7N 5B3. Electronic address: steve.wiseman@uleth.ca.</nlm:affiliation>
<country>Canada</country>
<wicri:regionArea>Toxicology Centre, University of Saskatchewan, 44 Campus Drive, Saskatoon, Saskatchewan</wicri:regionArea>
<wicri:noRegion>Saskatchewan</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Hecker, Markus" sort="Hecker, Markus" uniqKey="Hecker M" first="Markus" last="Hecker">Markus Hecker</name>
<affiliation wicri:level="1">
<nlm:affiliation>School of Environment and Sustainability, University of Saskatchewan, Room 323, Kirk Hall, 117 Science Place, Saskatoon, Saskatchewan, Canada S7N 5C8; Toxicology Centre, University of Saskatchewan, 44 Campus Drive, Saskatoon, Saskatchewan, Canada S7N 5B3. Electronic address: markus.hecker@usask.ca.</nlm:affiliation>
<country>Canada</country>
<wicri:regionArea>School of Environment and Sustainability, University of Saskatchewan, Room 323, Kirk Hall, 117 Science Place, Saskatoon, Saskatchewan, Canada S7N 5C8; Toxicology Centre, University of Saskatchewan, 44 Campus Drive, Saskatoon, Saskatchewan</wicri:regionArea>
<wicri:noRegion>Saskatchewan</wicri:noRegion>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PubMed</idno>
<date when="2016">2016</date>
<idno type="RBID">pubmed:27494256</idno>
<idno type="pmid">27494256</idno>
<idno type="doi">10.1016/j.ecoenv.2016.07.004</idno>
<idno type="wicri:Area/PubMed/Corpus">000029</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000029</idno>
<idno type="wicri:Area/PubMed/Curation">000029</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">000029</idno>
<idno type="wicri:Area/PubMed/Checkpoint">000029</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">000029</idno>
<idno type="wicri:Area/Ncbi/Merge">000724</idno>
<idno type="wicri:Area/Ncbi/Curation">000724</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">000724</idno>
<idno type="wicri:Area/Main/Merge">000053</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en">Is hepatic oxidative stress a main driver of dietary selenium toxicity in white sturgeon (Acipenser transmontanus)?</title>
<author>
<name sortKey="Zee, Jenna" sort="Zee, Jenna" uniqKey="Zee J" first="Jenna" last="Zee">Jenna Zee</name>
<affiliation wicri:level="1">
<nlm:affiliation>School of Environment and Sustainability, University of Saskatchewan, Room 323, Kirk Hall, 117 Science Place, Saskatoon, Saskatchewan, Canada S7N 5C8. Electronic address: jmz584@mail.usask.ca.</nlm:affiliation>
<country>Canada</country>
<wicri:regionArea>School of Environment and Sustainability, University of Saskatchewan, Room 323, Kirk Hall, 117 Science Place, Saskatoon, Saskatchewan</wicri:regionArea>
<wicri:noRegion>Saskatchewan</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Patterson, Sarah" sort="Patterson, Sarah" uniqKey="Patterson S" first="Sarah" last="Patterson">Sarah Patterson</name>
<affiliation wicri:level="1">
<nlm:affiliation>Toxicology Centre, University of Saskatchewan, 44 Campus Drive, Saskatoon, Saskatchewan, Canada S7N 5B3. Electronic address: sep662@mail.usask.ca.</nlm:affiliation>
<country>Canada</country>
<wicri:regionArea>Toxicology Centre, University of Saskatchewan, 44 Campus Drive, Saskatoon, Saskatchewan</wicri:regionArea>
<wicri:noRegion>Saskatchewan</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Wiseman, Steve" sort="Wiseman, Steve" uniqKey="Wiseman S" first="Steve" last="Wiseman">Steve Wiseman</name>
<affiliation wicri:level="1">
<nlm:affiliation>Toxicology Centre, University of Saskatchewan, 44 Campus Drive, Saskatoon, Saskatchewan, Canada S7N 5B3. Electronic address: steve.wiseman@uleth.ca.</nlm:affiliation>
<country>Canada</country>
<wicri:regionArea>Toxicology Centre, University of Saskatchewan, 44 Campus Drive, Saskatoon, Saskatchewan</wicri:regionArea>
<wicri:noRegion>Saskatchewan</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Hecker, Markus" sort="Hecker, Markus" uniqKey="Hecker M" first="Markus" last="Hecker">Markus Hecker</name>
<affiliation wicri:level="1">
<nlm:affiliation>School of Environment and Sustainability, University of Saskatchewan, Room 323, Kirk Hall, 117 Science Place, Saskatoon, Saskatchewan, Canada S7N 5C8; Toxicology Centre, University of Saskatchewan, 44 Campus Drive, Saskatoon, Saskatchewan, Canada S7N 5B3. Electronic address: markus.hecker@usask.ca.</nlm:affiliation>
<country>Canada</country>
<wicri:regionArea>School of Environment and Sustainability, University of Saskatchewan, Room 323, Kirk Hall, 117 Science Place, Saskatoon, Saskatchewan, Canada S7N 5C8; Toxicology Centre, University of Saskatchewan, 44 Campus Drive, Saskatoon, Saskatchewan</wicri:regionArea>
<wicri:noRegion>Saskatchewan</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Ecotoxicology and environmental safety</title>
<idno type="eISSN">1090-2414</idno>
<imprint>
<date when="2016" type="published">2016</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Animal Feed (analysis)</term>
<term>Animals</term>
<term>Chemical and Drug Induced Liver Injury (veterinary)</term>
<term>Diet</term>
<term>Dioxins (toxicity)</term>
<term>Fish Diseases (chemically induced)</term>
<term>Fishes</term>
<term>Glutathione Transferase (metabolism)</term>
<term>Oxidative Stress</term>
<term>Selenium (metabolism)</term>
<term>Selenium (toxicity)</term>
<term>Selenium Compounds</term>
<term>Selenomethionine (administration & dosage)</term>
<term>Selenomethionine (analysis)</term>
<term>Selenomethionine (toxicity)</term>
<term>Water Pollutants, Chemical (toxicity)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="administration & dosage" xml:lang="en">
<term>Selenomethionine</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en">
<term>Selenomethionine</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Glutathione Transferase</term>
<term>Selenium</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="toxicity" xml:lang="en">
<term>Dioxins</term>
<term>Selenium</term>
<term>Selenomethionine</term>
<term>Water Pollutants, Chemical</term>
</keywords>
<keywords scheme="MESH" qualifier="analysis" xml:lang="en">
<term>Animal Feed</term>
</keywords>
<keywords scheme="MESH" qualifier="chemically induced" xml:lang="en">
<term>Fish Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="veterinary" xml:lang="en">
<term>Chemical and Drug Induced Liver Injury</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Diet</term>
<term>Fishes</term>
<term>Oxidative Stress</term>
<term>Selenium Compounds</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Most species of sturgeon have experienced significant population declines and poor recruitment over the past decades, leading many, including white sturgeon (Acipenser transmontanus), to be listed as endangered. Reasons for these declines are not yet fully understood but benthic lifestyle, longevity, and delayed sexual maturation likely render sturgeon particularly susceptible to factors such as habitat alteration and contaminant exposures. One contaminant of particular concern to white sturgeon is selenium (Se), especially in its more bioavailable form selenomethionine (SeMet), as it is known to efficiently bioaccumulate in prey items of this species. Studies have shown white sturgeon to be among the most sensitive species of fish to dietary SeMet as well as other pollutants such as metals, dioxin-like chemicals and endocrine disrupters. One of the primary hypothesized mechanisms of toxicity of SeMet in fish is oxidative stress; however, little is know about the specific mode by which SeMet affects the health of white sturgeon. Therefore, the aim of this study was to characterize oxidative stress and associated antioxidant responses as a molecular event of toxicity, and to link it with the pathological effects observed previously. Specifically, three-year-old white sturgeon were exposed for 72 days via their diet to 1.4, 5.6, 22.4 or 104.4µg Se per g feed (dm). Doses were chosen to range over a necessary Se intake level, current environmentally relevant intakes and an intake representing predicted increases of Se release. Lipid hydroperoxides, which are end products of lipid oxidation, were quantified as a marker of oxidative stress. Changes in gene expression of glutathione peroxidase (GPx), superoxide dismutase, catalase, glutathione S-transferase, apoptosis inducing factor and caspase 3 were quantified as markers of the response to oxidative stress. Concentrations of lipid hydroperoxides were highly variable within dose groups and no dose response was observed. GPx expression was significantly increased in the low dose group indicating an induced antioxidant response. Expression of other genes were not significantly induced or suppressed. Overall, there was very little evidence of oxidative stress, and therefore, in contrast to previous reports on other species of teleost fishes, oxidative stress is not believed to be a main driver of toxicity in white sturgeon exposed to SeMet.</div>
</front>
</TEI>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Eau/explor/EsturgeonV1/Data/Main/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000053 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Merge/biblio.hfd -nk 000053 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Eau
   |area=    EsturgeonV1
   |flux=    Main
   |étape=   Merge
   |type=    RBID
   |clé=     pubmed:27494256
   |texte=   Is hepatic oxidative stress a main driver of dietary selenium toxicity in white sturgeon (Acipenser transmontanus)?
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Merge/RBID.i   -Sk "pubmed:27494256" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Merge/biblio.hfd   \
       | NlmPubMed2Wicri -a EsturgeonV1 

Wicri

This area was generated with Dilib version V0.6.27.
Data generation: Sat Mar 25 15:37:54 2017. Site generation: Tue Feb 13 14:18:49 2024