Nutrigenomic effects of glucosinolates on liver, muscle and distal kidney in parasite-free and salmon louse infected Atlantic salmon
Reduction of Lepeophtheirus salmonis infection in Atlantic salmon achieved by glucosinolates (GLs) from Brassica plants was recently reported. However, wider application of functional feeds based on GLs requires better knowledge of their positive and adverse effects. Liver, distal kidney and muscle...
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description | Reduction of Lepeophtheirus salmonis infection in Atlantic salmon achieved by glucosinolates (GLs) from Brassica plants was recently reported. However, wider application of functional feeds based on GLs requires better knowledge of their positive and adverse effects.
Liver, distal kidney and muscle transcriptomes of salmon exposed to the extreme dose of GLs were profiled by microarray, while qPCR analysis followed up selected hepatic and renal responses under the extreme and moderate GLs dose during the L. salmonis challenge. Transcriptional analysis were complemented with measurements of organ indices, liver steatosis and plasma profiling, including indicators of cytolysis and bilirubin. Finally, the third trial was performed to quantify the effect of lower GLs doses on growth.
The extreme GLs dose caused a decrease in hepatic fat deposition and growth, in line with microarray findings, which suggested tissue remodeling and reduction of cellular proliferation in the skeletal muscle and liver. Lower GLs inclusion levels in a follow-up trial did not show negative effects on growth. Microarray analysis of the distal kidney pointed to activation of anti-fibrotic responses under the overexposure. However, analyses of ALT, CK and AST enzymes in plasma provided no evidence of increased cytolysis and organ damage. Prevalent activation of phase-2 detoxification genes that occurred in all three tissues could be considered part of beneficial effects caused by the extreme dose of GLs. In addition, transcriptomic evidence suggested GLs-mediated iron and heme withdrawal response, including increased heme degradation in muscle (upregulation of heme oxygenase-1), decrease of its synthesis in liver (downregulation of porphobilinogen deaminase) and increased iron sequestration from blood (hepatic induction of hepcidin-1 and renal induction of intracellular storage protein ferritin). This response could be advantageous for salmon upon encountering lice, which depend on the host for the provision of iron carrying heme. Most of the hepatic genes studied by qPCR showed similar expression levels in fish exposed to GLs, lice and their combination, while renal induction of leptin suggested heightened stress by the combination of extreme dose of GLs and lice. High expression of interferon γ (cytokine considered organ-protective in mammalian kidney) was detected at the moderate GLs level. This fish also showed highest plasma bilirubin levels (degradation product of heme), and had l |
doi_str_mv | 10.1186/s13071-016-1921-7 |
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Liver, distal kidney and muscle transcriptomes of salmon exposed to the extreme dose of GLs were profiled by microarray, while qPCR analysis followed up selected hepatic and renal responses under the extreme and moderate GLs dose during the L. salmonis challenge. Transcriptional analysis were complemented with measurements of organ indices, liver steatosis and plasma profiling, including indicators of cytolysis and bilirubin. Finally, the third trial was performed to quantify the effect of lower GLs doses on growth.
The extreme GLs dose caused a decrease in hepatic fat deposition and growth, in line with microarray findings, which suggested tissue remodeling and reduction of cellular proliferation in the skeletal muscle and liver. Lower GLs inclusion levels in a follow-up trial did not show negative effects on growth. Microarray analysis of the distal kidney pointed to activation of anti-fibrotic responses under the overexposure. However, analyses of ALT, CK and AST enzymes in plasma provided no evidence of increased cytolysis and organ damage. Prevalent activation of phase-2 detoxification genes that occurred in all three tissues could be considered part of beneficial effects caused by the extreme dose of GLs. In addition, transcriptomic evidence suggested GLs-mediated iron and heme withdrawal response, including increased heme degradation in muscle (upregulation of heme oxygenase-1), decrease of its synthesis in liver (downregulation of porphobilinogen deaminase) and increased iron sequestration from blood (hepatic induction of hepcidin-1 and renal induction of intracellular storage protein ferritin). This response could be advantageous for salmon upon encountering lice, which depend on the host for the provision of iron carrying heme. Most of the hepatic genes studied by qPCR showed similar expression levels in fish exposed to GLs, lice and their combination, while renal induction of leptin suggested heightened stress by the combination of extreme dose of GLs and lice. High expression of interferon γ (cytokine considered organ-protective in mammalian kidney) was detected at the moderate GLs level. This fish also showed highest plasma bilirubin levels (degradation product of heme), and had lowest number of attached lice, further supporting hypothesis that making heme unavailable to lice could be part of an effective anti-parasitic strategy.
Modulation of detoxification and iron metabolism in Atlantic salmon tissues could be beneficial prior and during lice infestations. Investigation of anti-lice functional feeds based on low and moderate GLs inclusion levels thus deserves further attention.</description><identifier>ISSN: 1756-3305</identifier><identifier>EISSN: 1756-3305</identifier><identifier>DOI: 10.1186/s13071-016-1921-7</identifier><identifier>PMID: 27955686</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>adverse effects ; alanine transaminase ; Animal diseases ; Animals ; Antiparasitic Agents - administration & dosage ; Antiparasitic Agents - adverse effects ; aspartate transaminase ; Atlantic salmon ; bilirubin ; blood ; Brassica ; Care and treatment ; cell proliferation ; Copepoda - growth & development ; cytokines ; cytolysis ; Ectoparasitic Infestations - drug therapy ; Ectoparasitic Infestations - parasitology ; Ectoparasitic Infestations - veterinary ; fatty liver ; feeds ; ferritin ; Fish Diseases - drug therapy ; Fish Diseases - parasitology ; Gene Expression Profiling ; gene expression regulation ; genes ; glucosinolates ; Glucosinolates - administration & dosage ; Glucosinolates - adverse effects ; Glycosides ; Health aspects ; heme ; heme oxygenase (biliverdin-producing) ; interferon-gamma ; iron ; iron absorption ; Kidney - drug effects ; Kidney - pathology ; kidneys ; Lepeophtheirus salmonis ; leptin ; lice ; lice infestations ; liver ; Liver - drug effects ; Liver - pathology ; mammals ; Microarray Analysis ; microarray technology ; muscles ; Muscles - drug effects ; Muscles - pathology ; Nutrigenomics ; porphobilinogen ; quantitative polymerase chain reaction ; Real-Time Polymerase Chain Reaction ; Salmo salar ; salmon ; skeletal muscle ; transcription (genetics) ; transcriptome ; transcriptomics</subject><ispartof>Parasites & vectors, 2016-12, Vol.9 (1), p.639-639, Article 639</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2016</rights><rights>The Author(s). 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4487-a1bec87e3f32ce2787c02d78a9c5651968e3324a46003dea303a1fc5c626545a3</citedby><cites>FETCH-LOGICAL-c4487-a1bec87e3f32ce2787c02d78a9c5651968e3324a46003dea303a1fc5c626545a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153675/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153675/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,27911,27912,53778,53780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27955686$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Skugor, Stanko</creatorcontrib><creatorcontrib>Jodaa Holm, Helle</creatorcontrib><creatorcontrib>Bjelland, Anne Kari</creatorcontrib><creatorcontrib>Pino, Jorge</creatorcontrib><creatorcontrib>Evensen, Øystein</creatorcontrib><creatorcontrib>Krasnov, Aleksei</creatorcontrib><creatorcontrib>Wadsworth, Simon</creatorcontrib><title>Nutrigenomic effects of glucosinolates on liver, muscle and distal kidney in parasite-free and salmon louse infected Atlantic salmon</title><title>Parasites & vectors</title><addtitle>Parasit Vectors</addtitle><description>Reduction of Lepeophtheirus salmonis infection in Atlantic salmon achieved by glucosinolates (GLs) from Brassica plants was recently reported. However, wider application of functional feeds based on GLs requires better knowledge of their positive and adverse effects.
Liver, distal kidney and muscle transcriptomes of salmon exposed to the extreme dose of GLs were profiled by microarray, while qPCR analysis followed up selected hepatic and renal responses under the extreme and moderate GLs dose during the L. salmonis challenge. Transcriptional analysis were complemented with measurements of organ indices, liver steatosis and plasma profiling, including indicators of cytolysis and bilirubin. Finally, the third trial was performed to quantify the effect of lower GLs doses on growth.
The extreme GLs dose caused a decrease in hepatic fat deposition and growth, in line with microarray findings, which suggested tissue remodeling and reduction of cellular proliferation in the skeletal muscle and liver. Lower GLs inclusion levels in a follow-up trial did not show negative effects on growth. Microarray analysis of the distal kidney pointed to activation of anti-fibrotic responses under the overexposure. However, analyses of ALT, CK and AST enzymes in plasma provided no evidence of increased cytolysis and organ damage. Prevalent activation of phase-2 detoxification genes that occurred in all three tissues could be considered part of beneficial effects caused by the extreme dose of GLs. In addition, transcriptomic evidence suggested GLs-mediated iron and heme withdrawal response, including increased heme degradation in muscle (upregulation of heme oxygenase-1), decrease of its synthesis in liver (downregulation of porphobilinogen deaminase) and increased iron sequestration from blood (hepatic induction of hepcidin-1 and renal induction of intracellular storage protein ferritin). This response could be advantageous for salmon upon encountering lice, which depend on the host for the provision of iron carrying heme. Most of the hepatic genes studied by qPCR showed similar expression levels in fish exposed to GLs, lice and their combination, while renal induction of leptin suggested heightened stress by the combination of extreme dose of GLs and lice. High expression of interferon γ (cytokine considered organ-protective in mammalian kidney) was detected at the moderate GLs level. This fish also showed highest plasma bilirubin levels (degradation product of heme), and had lowest number of attached lice, further supporting hypothesis that making heme unavailable to lice could be part of an effective anti-parasitic strategy.
Modulation of detoxification and iron metabolism in Atlantic salmon tissues could be beneficial prior and during lice infestations. Investigation of anti-lice functional feeds based on low and moderate GLs inclusion levels thus deserves further attention.</description><subject>adverse effects</subject><subject>alanine transaminase</subject><subject>Animal diseases</subject><subject>Animals</subject><subject>Antiparasitic Agents - administration & dosage</subject><subject>Antiparasitic Agents - adverse effects</subject><subject>aspartate transaminase</subject><subject>Atlantic salmon</subject><subject>bilirubin</subject><subject>blood</subject><subject>Brassica</subject><subject>Care and treatment</subject><subject>cell proliferation</subject><subject>Copepoda - growth & development</subject><subject>cytokines</subject><subject>cytolysis</subject><subject>Ectoparasitic Infestations - drug therapy</subject><subject>Ectoparasitic Infestations - parasitology</subject><subject>Ectoparasitic Infestations - veterinary</subject><subject>fatty liver</subject><subject>feeds</subject><subject>ferritin</subject><subject>Fish Diseases - drug therapy</subject><subject>Fish Diseases - parasitology</subject><subject>Gene Expression Profiling</subject><subject>gene expression regulation</subject><subject>genes</subject><subject>glucosinolates</subject><subject>Glucosinolates - administration & dosage</subject><subject>Glucosinolates - adverse effects</subject><subject>Glycosides</subject><subject>Health aspects</subject><subject>heme</subject><subject>heme oxygenase (biliverdin-producing)</subject><subject>interferon-gamma</subject><subject>iron</subject><subject>iron absorption</subject><subject>Kidney - drug effects</subject><subject>Kidney - pathology</subject><subject>kidneys</subject><subject>Lepeophtheirus salmonis</subject><subject>leptin</subject><subject>lice</subject><subject>lice infestations</subject><subject>liver</subject><subject>Liver - drug effects</subject><subject>Liver - pathology</subject><subject>mammals</subject><subject>Microarray Analysis</subject><subject>microarray technology</subject><subject>muscles</subject><subject>Muscles - drug effects</subject><subject>Muscles - pathology</subject><subject>Nutrigenomics</subject><subject>porphobilinogen</subject><subject>quantitative polymerase chain reaction</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Salmo salar</subject><subject>salmon</subject><subject>skeletal muscle</subject><subject>transcription (genetics)</subject><subject>transcriptome</subject><subject>transcriptomics</subject><issn>1756-3305</issn><issn>1756-3305</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNqFkktrFTEUxwdRbK1-ADcScKPg1Dwmj9kIl-KjUBR8rEOaOXNNzSS3SabYvR_cjFNLrxvJIuGc3_-c5OTfNE8JPiZEideZMCxJi4loSU9JK-81h0Ry0TKG-f0754PmUc4XGAvcc_GwOaCy51wocdj8-jiX5LYQ4uQsgnEEWzKKI9r62cbsQvSmQI0E5N0VpFdomrP1gEwY0OByMR79cEOAa-QC2plksivQjglWJBs_Ldo4Z6jEUh4GtCnehFIbrunHzYPR-AxPbvaj5tu7t19PPrRnn96fnmzOWtt1SraGnINVEtjIqAUqlbSYDlKZ3nLBSS8UMEY70wmM2QCGYWbIaLkVVPCOG3bUvFnr7ubzCQYLoSTj9S65yaRrHY3T-5ngvuttvNKccCYkrwVe3BRI8XKGXPTksgVfXwP1hZpijDvVY6r-ixLFCVWdYAv6_B_0Is4p1EkslCC19Z_exyu1NR50HWWsV7R1DVC_LgYYXY1vOoV5J6XAVfByT1CZAj_L1sw569Mvn_dZsrI2xZwTjLdDIVgvXtOr13T1ml68pmXVPLs7zVvFX3Ox322Tz70</recordid><startdate>20161212</startdate><enddate>20161212</enddate><creator>Skugor, Stanko</creator><creator>Jodaa Holm, Helle</creator><creator>Bjelland, Anne Kari</creator><creator>Pino, Jorge</creator><creator>Evensen, Øystein</creator><creator>Krasnov, Aleksei</creator><creator>Wadsworth, Simon</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7SN</scope><scope>7SS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H95</scope><scope>K9.</scope><scope>L.G</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20161212</creationdate><title>Nutrigenomic effects of glucosinolates on liver, muscle and distal kidney in parasite-free and salmon louse infected Atlantic salmon</title><author>Skugor, Stanko ; Jodaa Holm, Helle ; Bjelland, Anne Kari ; Pino, Jorge ; Evensen, Øystein ; Krasnov, Aleksei ; Wadsworth, Simon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4487-a1bec87e3f32ce2787c02d78a9c5651968e3324a46003dea303a1fc5c626545a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>adverse effects</topic><topic>alanine transaminase</topic><topic>Animal diseases</topic><topic>Animals</topic><topic>Antiparasitic Agents - administration & dosage</topic><topic>Antiparasitic Agents - adverse effects</topic><topic>aspartate transaminase</topic><topic>Atlantic salmon</topic><topic>bilirubin</topic><topic>blood</topic><topic>Brassica</topic><topic>Care and treatment</topic><topic>cell proliferation</topic><topic>Copepoda - growth & development</topic><topic>cytokines</topic><topic>cytolysis</topic><topic>Ectoparasitic Infestations - drug therapy</topic><topic>Ectoparasitic Infestations - parasitology</topic><topic>Ectoparasitic Infestations - veterinary</topic><topic>fatty liver</topic><topic>feeds</topic><topic>ferritin</topic><topic>Fish Diseases - drug therapy</topic><topic>Fish Diseases - parasitology</topic><topic>Gene Expression Profiling</topic><topic>gene expression regulation</topic><topic>genes</topic><topic>glucosinolates</topic><topic>Glucosinolates - administration & dosage</topic><topic>Glucosinolates - adverse effects</topic><topic>Glycosides</topic><topic>Health aspects</topic><topic>heme</topic><topic>heme oxygenase (biliverdin-producing)</topic><topic>interferon-gamma</topic><topic>iron</topic><topic>iron absorption</topic><topic>Kidney - drug effects</topic><topic>Kidney - pathology</topic><topic>kidneys</topic><topic>Lepeophtheirus salmonis</topic><topic>leptin</topic><topic>lice</topic><topic>lice infestations</topic><topic>liver</topic><topic>Liver - drug effects</topic><topic>Liver - pathology</topic><topic>mammals</topic><topic>Microarray Analysis</topic><topic>microarray technology</topic><topic>muscles</topic><topic>Muscles - drug effects</topic><topic>Muscles - pathology</topic><topic>Nutrigenomics</topic><topic>porphobilinogen</topic><topic>quantitative polymerase chain reaction</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Salmo salar</topic><topic>salmon</topic><topic>skeletal muscle</topic><topic>transcription (genetics)</topic><topic>transcriptome</topic><topic>transcriptomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Skugor, Stanko</creatorcontrib><creatorcontrib>Jodaa Holm, Helle</creatorcontrib><creatorcontrib>Bjelland, Anne Kari</creatorcontrib><creatorcontrib>Pino, Jorge</creatorcontrib><creatorcontrib>Evensen, Øystein</creatorcontrib><creatorcontrib>Krasnov, Aleksei</creatorcontrib><creatorcontrib>Wadsworth, Simon</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Parasites & vectors</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Skugor, Stanko</au><au>Jodaa Holm, Helle</au><au>Bjelland, Anne Kari</au><au>Pino, Jorge</au><au>Evensen, Øystein</au><au>Krasnov, Aleksei</au><au>Wadsworth, Simon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nutrigenomic effects of glucosinolates on liver, muscle and distal kidney in parasite-free and salmon louse infected Atlantic salmon</atitle><jtitle>Parasites & vectors</jtitle><addtitle>Parasit Vectors</addtitle><date>2016-12-12</date><risdate>2016</risdate><volume>9</volume><issue>1</issue><spage>639</spage><epage>639</epage><pages>639-639</pages><artnum>639</artnum><issn>1756-3305</issn><eissn>1756-3305</eissn><abstract>Reduction of Lepeophtheirus salmonis infection in Atlantic salmon achieved by glucosinolates (GLs) from Brassica plants was recently reported. However, wider application of functional feeds based on GLs requires better knowledge of their positive and adverse effects.
Liver, distal kidney and muscle transcriptomes of salmon exposed to the extreme dose of GLs were profiled by microarray, while qPCR analysis followed up selected hepatic and renal responses under the extreme and moderate GLs dose during the L. salmonis challenge. Transcriptional analysis were complemented with measurements of organ indices, liver steatosis and plasma profiling, including indicators of cytolysis and bilirubin. Finally, the third trial was performed to quantify the effect of lower GLs doses on growth.
The extreme GLs dose caused a decrease in hepatic fat deposition and growth, in line with microarray findings, which suggested tissue remodeling and reduction of cellular proliferation in the skeletal muscle and liver. Lower GLs inclusion levels in a follow-up trial did not show negative effects on growth. Microarray analysis of the distal kidney pointed to activation of anti-fibrotic responses under the overexposure. However, analyses of ALT, CK and AST enzymes in plasma provided no evidence of increased cytolysis and organ damage. Prevalent activation of phase-2 detoxification genes that occurred in all three tissues could be considered part of beneficial effects caused by the extreme dose of GLs. In addition, transcriptomic evidence suggested GLs-mediated iron and heme withdrawal response, including increased heme degradation in muscle (upregulation of heme oxygenase-1), decrease of its synthesis in liver (downregulation of porphobilinogen deaminase) and increased iron sequestration from blood (hepatic induction of hepcidin-1 and renal induction of intracellular storage protein ferritin). This response could be advantageous for salmon upon encountering lice, which depend on the host for the provision of iron carrying heme. Most of the hepatic genes studied by qPCR showed similar expression levels in fish exposed to GLs, lice and their combination, while renal induction of leptin suggested heightened stress by the combination of extreme dose of GLs and lice. High expression of interferon γ (cytokine considered organ-protective in mammalian kidney) was detected at the moderate GLs level. This fish also showed highest plasma bilirubin levels (degradation product of heme), and had lowest number of attached lice, further supporting hypothesis that making heme unavailable to lice could be part of an effective anti-parasitic strategy.
Modulation of detoxification and iron metabolism in Atlantic salmon tissues could be beneficial prior and during lice infestations. Investigation of anti-lice functional feeds based on low and moderate GLs inclusion levels thus deserves further attention.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>27955686</pmid><doi>10.1186/s13071-016-1921-7</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5153675 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Springer Nature OA Free Journals; Springer Nature - Complete Springer Journals; PubMed Central |
subjects | adverse effects alanine transaminase Animal diseases Animals Antiparasitic Agents - administration & dosage Antiparasitic Agents - adverse effects aspartate transaminase Atlantic salmon bilirubin blood Brassica Care and treatment cell proliferation Copepoda - growth & development cytokines cytolysis Ectoparasitic Infestations - drug therapy Ectoparasitic Infestations - parasitology Ectoparasitic Infestations - veterinary fatty liver feeds ferritin Fish Diseases - drug therapy Fish Diseases - parasitology Gene Expression Profiling gene expression regulation genes glucosinolates Glucosinolates - administration & dosage Glucosinolates - adverse effects Glycosides Health aspects heme heme oxygenase (biliverdin-producing) interferon-gamma iron iron absorption Kidney - drug effects Kidney - pathology kidneys Lepeophtheirus salmonis leptin lice lice infestations liver Liver - drug effects Liver - pathology mammals Microarray Analysis microarray technology muscles Muscles - drug effects Muscles - pathology Nutrigenomics porphobilinogen quantitative polymerase chain reaction Real-Time Polymerase Chain Reaction Salmo salar salmon skeletal muscle transcription (genetics) transcriptome transcriptomics |
title | Nutrigenomic effects of glucosinolates on liver, muscle and distal kidney in parasite-free and salmon louse infected Atlantic salmon |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T01%3A03%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Nutrigenomic%20effects%20of%20glucosinolates%20on%20liver,%20muscle%20and%20distal%20kidney%20in%20parasite-free%20and%20salmon%20louse%20infected%20Atlantic%20salmon&rft.jtitle=Parasites%20&%20vectors&rft.au=Skugor,%20Stanko&rft.date=2016-12-12&rft.volume=9&rft.issue=1&rft.spage=639&rft.epage=639&rft.pages=639-639&rft.artnum=639&rft.issn=1756-3305&rft.eissn=1756-3305&rft_id=info:doi/10.1186/s13071-016-1921-7&rft_dat=%3Cgale_pubme%3EA480547760%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1856136775&rft_id=info:pmid/27955686&rft_galeid=A480547760&rfr_iscdi=true |