Transcriptional and cellular effects of benzotriazole UV stabilizers UV‐234 and UV‐328 in the freshwater invertebrates Chlamydomonas reinhardtii and Daphnia magna

Benzotriazole ultra violet stabilizers (BZT‐UVs) are compounds used in many applications and products to prevent photochemical degradation. Despite their widespread presence in aquatic ecosystems and persistence in the environment, there are very limited data on their effects and toxicity, and their...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Environmental toxicology and chemistry 2017-12, Vol.36 (12), p.3333-3342
Hauptverfasser: Giraudo, Maeva, Cottin, Guillaume, Esperanza, Marta, Gagnon, Pierre, Silva, Amila O. De, Houde, Magali
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3342
container_issue 12
container_start_page 3333
container_title Environmental toxicology and chemistry
container_volume 36
creator Giraudo, Maeva
Cottin, Guillaume
Esperanza, Marta
Gagnon, Pierre
Silva, Amila O. De
Houde, Magali
description Benzotriazole ultra violet stabilizers (BZT‐UVs) are compounds used in many applications and products to prevent photochemical degradation. Despite their widespread presence in aquatic ecosystems and persistence in the environment, there are very limited data on their effects and toxicity, and their modes of action remain largely unknown. The objectives of the present study were to evaluate the chronic effects of 2 BZT‐UVs, 2‐(2H‐benzotriazol‐2‐yl)‐4,6‐bis(1‐methyl‐1‐phenylethyl)phenol (UV‐234) and 2‐(2H‐benzotriazol‐2‐yl)‐4,6‐di‐tert‐pentylphenol (UV‐328), on the freshwater green algae Chlamydomonas reinhardtii and the freshwater crustacean Daphnia magna. Organisms were exposed to 0.01 and 10 μg/L of UV‐234, UV‐328, as well as a mixture of the 2 compounds. Life‐history endpoints (viability, reproduction, and growth) and oxidative stress–related biomarkers (gene transcription, reactive oxygen species [ROS] production, and lipid peroxidation) were measured. Daphnia magna growth, reproduction, and gene transcription were not impacted by 21‐d individual or mixed exposure. After 96‐h of exposure, no differences were observed on the cellular viability of C. reinhardtii for either of the 2 BZT‐UVs. In the algae, results showed increased ROS production in response to UV‐328 and lipid peroxidation following exposure to UV‐234. Synergistic effects of the 2 BZT‐UVs were evident at the transcriptional level with 2 to 6 times up‐regulation of glutathione peroxidase (gpx) in response to the mixture for all treatment conditions. The transcription of superoxide dismutase (sod), catalase (cat), and ascorbic peroxidase (apx) was also regulated by UV‐234 and UV‐328 in the green algae, most likely as a result of ROS production and lipid peroxidation. Results from the present study suggest potential impacts of UV‐234 and UV‐328 exposure on the antioxidant defense system in C. reinhardtii. Environ Toxicol Chem 2017;36:3333–3342. © 2017 Crown in the Right of Canada. Published by Wiley Periodicals Inc., on behalf of SETAC.
doi_str_mv 10.1002/etc.3908
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1968583714</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1968583714</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3868-e474f24ebf7d5bf8e38fad44176f932848ed2fefa451bf28d4387061e66d0f753</originalsourceid><addsrcrecordid>eNp1kc1O3DAURq0KVKa0Up8AWWLTTcB_sZ0lGlpaCakb6DZy4uvGyEkG2wOaWfUR-hR9MJ6kZga668r6rOPjq_sh9JGSM0oIO4fcn_GG6DdoQeuaVVpSfYAWRHFSKSb1EXqX0h0hVDZN8xYdMa2IZoos0J-baKbUR7_Kfp5MwGayuIcQ1sFEDM5BnxOeHe5g2s45erOdA-DbHzhl0_ngtxBTiU-_fjMudq93gTON_YTzANhFSMOjyRDLzQPEDF0sKeHlEMy4sfNYPk44gp8GE232fqe5NKth8gaP5udk3qNDZ0KCDy_nMbr98vlm-bW6_n71bXlxXfVcS12BUMIxAZ1Ttu6cBq6dsUJQJV1TRhIaLHPgjKhp55i2gpdNSApSWuJUzY_R6d67ivP9GlJu7-Z1LHtJLW2krjVXVBTq057q45xSBNeuoh9N3LSUtM-FtKWQ9rmQgp68CNfdCPYf-NpAAao98OgDbP4raguzE_4FY_CY1A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1968583714</pqid></control><display><type>article</type><title>Transcriptional and cellular effects of benzotriazole UV stabilizers UV‐234 and UV‐328 in the freshwater invertebrates Chlamydomonas reinhardtii and Daphnia magna</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Giraudo, Maeva ; Cottin, Guillaume ; Esperanza, Marta ; Gagnon, Pierre ; Silva, Amila O. De ; Houde, Magali</creator><creatorcontrib>Giraudo, Maeva ; Cottin, Guillaume ; Esperanza, Marta ; Gagnon, Pierre ; Silva, Amila O. De ; Houde, Magali</creatorcontrib><description>Benzotriazole ultra violet stabilizers (BZT‐UVs) are compounds used in many applications and products to prevent photochemical degradation. Despite their widespread presence in aquatic ecosystems and persistence in the environment, there are very limited data on their effects and toxicity, and their modes of action remain largely unknown. The objectives of the present study were to evaluate the chronic effects of 2 BZT‐UVs, 2‐(2H‐benzotriazol‐2‐yl)‐4,6‐bis(1‐methyl‐1‐phenylethyl)phenol (UV‐234) and 2‐(2H‐benzotriazol‐2‐yl)‐4,6‐di‐tert‐pentylphenol (UV‐328), on the freshwater green algae Chlamydomonas reinhardtii and the freshwater crustacean Daphnia magna. Organisms were exposed to 0.01 and 10 μg/L of UV‐234, UV‐328, as well as a mixture of the 2 compounds. Life‐history endpoints (viability, reproduction, and growth) and oxidative stress–related biomarkers (gene transcription, reactive oxygen species [ROS] production, and lipid peroxidation) were measured. Daphnia magna growth, reproduction, and gene transcription were not impacted by 21‐d individual or mixed exposure. After 96‐h of exposure, no differences were observed on the cellular viability of C. reinhardtii for either of the 2 BZT‐UVs. In the algae, results showed increased ROS production in response to UV‐328 and lipid peroxidation following exposure to UV‐234. Synergistic effects of the 2 BZT‐UVs were evident at the transcriptional level with 2 to 6 times up‐regulation of glutathione peroxidase (gpx) in response to the mixture for all treatment conditions. The transcription of superoxide dismutase (sod), catalase (cat), and ascorbic peroxidase (apx) was also regulated by UV‐234 and UV‐328 in the green algae, most likely as a result of ROS production and lipid peroxidation. Results from the present study suggest potential impacts of UV‐234 and UV‐328 exposure on the antioxidant defense system in C. reinhardtii. Environ Toxicol Chem 2017;36:3333–3342. © 2017 Crown in the Right of Canada. Published by Wiley Periodicals Inc., on behalf of SETAC.</description><identifier>ISSN: 0730-7268</identifier><identifier>EISSN: 1552-8618</identifier><identifier>DOI: 10.1002/etc.3908</identifier><identifier>PMID: 28708270</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Algae ; Animals ; Antioxidants ; Antioxidants - metabolism ; Aquatic ecosystems ; Aquatic plants ; Aquatic toxicology ; Ascorbate Peroxidases - metabolism ; Benzotriazole ; Benzotriazole UV stabilizers ; Biodegradation ; Biomarkers ; Catalase ; Catalase - metabolism ; Chlamydomonas reinhardtii ; Chlamydomonas reinhardtii - drug effects ; Chlamydomonas reinhardtii - genetics ; Chlorophyta ; Chronic effects ; Contaminant of emerging concern ; Crustaceans ; Daphnia - drug effects ; Daphnia - genetics ; Daphnia - metabolism ; Daphnia magna ; Exposure ; Fresh Water ; Freshwater crustaceans ; Freshwater invertebrates ; Freshwater organisms ; Glutathione ; Glutathione peroxidase ; Glutathione Peroxidase - metabolism ; Invertebrates ; Life Cycle Stages ; Life history ; Lipid peroxidation ; Lipid Peroxidation - drug effects ; Lipids ; Oxidative stress ; Oxidative Stress - drug effects ; Peroxidase ; Peroxidation ; Phenols ; Photochemicals ; Reactive oxygen species ; Reactive Oxygen Species - metabolism ; Reproduction (biology) ; Reproduction - drug effects ; Shellfish ; Superoxide dismutase ; Superoxide Dismutase - metabolism ; Synergistic effect ; Toxicity ; Transcription ; Transcription, Genetic ; Transcriptomics ; Triazoles - toxicity ; Ultraviolet radiation ; Up-Regulation ; UV stabilizers</subject><ispartof>Environmental toxicology and chemistry, 2017-12, Vol.36 (12), p.3333-3342</ispartof><rights>2017 Crown in the Right of Canada. Published by Wiley Periodicals Inc., on behalf of SETAC.</rights><rights>2017 SETAC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3868-e474f24ebf7d5bf8e38fad44176f932848ed2fefa451bf28d4387061e66d0f753</citedby><cites>FETCH-LOGICAL-c3868-e474f24ebf7d5bf8e38fad44176f932848ed2fefa451bf28d4387061e66d0f753</cites><orcidid>0000-0003-4296-146X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fetc.3908$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fetc.3908$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28708270$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Giraudo, Maeva</creatorcontrib><creatorcontrib>Cottin, Guillaume</creatorcontrib><creatorcontrib>Esperanza, Marta</creatorcontrib><creatorcontrib>Gagnon, Pierre</creatorcontrib><creatorcontrib>Silva, Amila O. De</creatorcontrib><creatorcontrib>Houde, Magali</creatorcontrib><title>Transcriptional and cellular effects of benzotriazole UV stabilizers UV‐234 and UV‐328 in the freshwater invertebrates Chlamydomonas reinhardtii and Daphnia magna</title><title>Environmental toxicology and chemistry</title><addtitle>Environ Toxicol Chem</addtitle><description>Benzotriazole ultra violet stabilizers (BZT‐UVs) are compounds used in many applications and products to prevent photochemical degradation. Despite their widespread presence in aquatic ecosystems and persistence in the environment, there are very limited data on their effects and toxicity, and their modes of action remain largely unknown. The objectives of the present study were to evaluate the chronic effects of 2 BZT‐UVs, 2‐(2H‐benzotriazol‐2‐yl)‐4,6‐bis(1‐methyl‐1‐phenylethyl)phenol (UV‐234) and 2‐(2H‐benzotriazol‐2‐yl)‐4,6‐di‐tert‐pentylphenol (UV‐328), on the freshwater green algae Chlamydomonas reinhardtii and the freshwater crustacean Daphnia magna. Organisms were exposed to 0.01 and 10 μg/L of UV‐234, UV‐328, as well as a mixture of the 2 compounds. Life‐history endpoints (viability, reproduction, and growth) and oxidative stress–related biomarkers (gene transcription, reactive oxygen species [ROS] production, and lipid peroxidation) were measured. Daphnia magna growth, reproduction, and gene transcription were not impacted by 21‐d individual or mixed exposure. After 96‐h of exposure, no differences were observed on the cellular viability of C. reinhardtii for either of the 2 BZT‐UVs. In the algae, results showed increased ROS production in response to UV‐328 and lipid peroxidation following exposure to UV‐234. Synergistic effects of the 2 BZT‐UVs were evident at the transcriptional level with 2 to 6 times up‐regulation of glutathione peroxidase (gpx) in response to the mixture for all treatment conditions. The transcription of superoxide dismutase (sod), catalase (cat), and ascorbic peroxidase (apx) was also regulated by UV‐234 and UV‐328 in the green algae, most likely as a result of ROS production and lipid peroxidation. Results from the present study suggest potential impacts of UV‐234 and UV‐328 exposure on the antioxidant defense system in C. reinhardtii. Environ Toxicol Chem 2017;36:3333–3342. © 2017 Crown in the Right of Canada. Published by Wiley Periodicals Inc., on behalf of SETAC.</description><subject>Algae</subject><subject>Animals</subject><subject>Antioxidants</subject><subject>Antioxidants - metabolism</subject><subject>Aquatic ecosystems</subject><subject>Aquatic plants</subject><subject>Aquatic toxicology</subject><subject>Ascorbate Peroxidases - metabolism</subject><subject>Benzotriazole</subject><subject>Benzotriazole UV stabilizers</subject><subject>Biodegradation</subject><subject>Biomarkers</subject><subject>Catalase</subject><subject>Catalase - metabolism</subject><subject>Chlamydomonas reinhardtii</subject><subject>Chlamydomonas reinhardtii - drug effects</subject><subject>Chlamydomonas reinhardtii - genetics</subject><subject>Chlorophyta</subject><subject>Chronic effects</subject><subject>Contaminant of emerging concern</subject><subject>Crustaceans</subject><subject>Daphnia - drug effects</subject><subject>Daphnia - genetics</subject><subject>Daphnia - metabolism</subject><subject>Daphnia magna</subject><subject>Exposure</subject><subject>Fresh Water</subject><subject>Freshwater crustaceans</subject><subject>Freshwater invertebrates</subject><subject>Freshwater organisms</subject><subject>Glutathione</subject><subject>Glutathione peroxidase</subject><subject>Glutathione Peroxidase - metabolism</subject><subject>Invertebrates</subject><subject>Life Cycle Stages</subject><subject>Life history</subject><subject>Lipid peroxidation</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Lipids</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Peroxidase</subject><subject>Peroxidation</subject><subject>Phenols</subject><subject>Photochemicals</subject><subject>Reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Reproduction (biology)</subject><subject>Reproduction - drug effects</subject><subject>Shellfish</subject><subject>Superoxide dismutase</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Synergistic effect</subject><subject>Toxicity</subject><subject>Transcription</subject><subject>Transcription, Genetic</subject><subject>Transcriptomics</subject><subject>Triazoles - toxicity</subject><subject>Ultraviolet radiation</subject><subject>Up-Regulation</subject><subject>UV stabilizers</subject><issn>0730-7268</issn><issn>1552-8618</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1O3DAURq0KVKa0Up8AWWLTTcB_sZ0lGlpaCakb6DZy4uvGyEkG2wOaWfUR-hR9MJ6kZga668r6rOPjq_sh9JGSM0oIO4fcn_GG6DdoQeuaVVpSfYAWRHFSKSb1EXqX0h0hVDZN8xYdMa2IZoos0J-baKbUR7_Kfp5MwGayuIcQ1sFEDM5BnxOeHe5g2s45erOdA-DbHzhl0_ngtxBTiU-_fjMudq93gTON_YTzANhFSMOjyRDLzQPEDF0sKeHlEMy4sfNYPk44gp8GE232fqe5NKth8gaP5udk3qNDZ0KCDy_nMbr98vlm-bW6_n71bXlxXfVcS12BUMIxAZ1Ttu6cBq6dsUJQJV1TRhIaLHPgjKhp55i2gpdNSApSWuJUzY_R6d67ivP9GlJu7-Z1LHtJLW2krjVXVBTq057q45xSBNeuoh9N3LSUtM-FtKWQ9rmQgp68CNfdCPYf-NpAAao98OgDbP4raguzE_4FY_CY1A</recordid><startdate>201712</startdate><enddate>201712</enddate><creator>Giraudo, Maeva</creator><creator>Cottin, Guillaume</creator><creator>Esperanza, Marta</creator><creator>Gagnon, Pierre</creator><creator>Silva, Amila O. De</creator><creator>Houde, Magali</creator><general>Blackwell Publishing Ltd</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>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><orcidid>https://orcid.org/0000-0003-4296-146X</orcidid></search><sort><creationdate>201712</creationdate><title>Transcriptional and cellular effects of benzotriazole UV stabilizers UV‐234 and UV‐328 in the freshwater invertebrates Chlamydomonas reinhardtii and Daphnia magna</title><author>Giraudo, Maeva ; Cottin, Guillaume ; Esperanza, Marta ; Gagnon, Pierre ; Silva, Amila O. De ; Houde, Magali</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3868-e474f24ebf7d5bf8e38fad44176f932848ed2fefa451bf28d4387061e66d0f753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Algae</topic><topic>Animals</topic><topic>Antioxidants</topic><topic>Antioxidants - metabolism</topic><topic>Aquatic ecosystems</topic><topic>Aquatic plants</topic><topic>Aquatic toxicology</topic><topic>Ascorbate Peroxidases - metabolism</topic><topic>Benzotriazole</topic><topic>Benzotriazole UV stabilizers</topic><topic>Biodegradation</topic><topic>Biomarkers</topic><topic>Catalase</topic><topic>Catalase - metabolism</topic><topic>Chlamydomonas reinhardtii</topic><topic>Chlamydomonas reinhardtii - drug effects</topic><topic>Chlamydomonas reinhardtii - genetics</topic><topic>Chlorophyta</topic><topic>Chronic effects</topic><topic>Contaminant of emerging concern</topic><topic>Crustaceans</topic><topic>Daphnia - drug effects</topic><topic>Daphnia - genetics</topic><topic>Daphnia - metabolism</topic><topic>Daphnia magna</topic><topic>Exposure</topic><topic>Fresh Water</topic><topic>Freshwater crustaceans</topic><topic>Freshwater invertebrates</topic><topic>Freshwater organisms</topic><topic>Glutathione</topic><topic>Glutathione peroxidase</topic><topic>Glutathione Peroxidase - metabolism</topic><topic>Invertebrates</topic><topic>Life Cycle Stages</topic><topic>Life history</topic><topic>Lipid peroxidation</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Lipids</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Peroxidase</topic><topic>Peroxidation</topic><topic>Phenols</topic><topic>Photochemicals</topic><topic>Reactive oxygen species</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Reproduction (biology)</topic><topic>Reproduction - drug effects</topic><topic>Shellfish</topic><topic>Superoxide dismutase</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Synergistic effect</topic><topic>Toxicity</topic><topic>Transcription</topic><topic>Transcription, Genetic</topic><topic>Transcriptomics</topic><topic>Triazoles - toxicity</topic><topic>Ultraviolet radiation</topic><topic>Up-Regulation</topic><topic>UV stabilizers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Giraudo, Maeva</creatorcontrib><creatorcontrib>Cottin, Guillaume</creatorcontrib><creatorcontrib>Esperanza, Marta</creatorcontrib><creatorcontrib>Gagnon, Pierre</creatorcontrib><creatorcontrib>Silva, Amila O. De</creatorcontrib><creatorcontrib>Houde, Magali</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><jtitle>Environmental toxicology and chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Giraudo, Maeva</au><au>Cottin, Guillaume</au><au>Esperanza, Marta</au><au>Gagnon, Pierre</au><au>Silva, Amila O. De</au><au>Houde, Magali</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transcriptional and cellular effects of benzotriazole UV stabilizers UV‐234 and UV‐328 in the freshwater invertebrates Chlamydomonas reinhardtii and Daphnia magna</atitle><jtitle>Environmental toxicology and chemistry</jtitle><addtitle>Environ Toxicol Chem</addtitle><date>2017-12</date><risdate>2017</risdate><volume>36</volume><issue>12</issue><spage>3333</spage><epage>3342</epage><pages>3333-3342</pages><issn>0730-7268</issn><eissn>1552-8618</eissn><abstract>Benzotriazole ultra violet stabilizers (BZT‐UVs) are compounds used in many applications and products to prevent photochemical degradation. Despite their widespread presence in aquatic ecosystems and persistence in the environment, there are very limited data on their effects and toxicity, and their modes of action remain largely unknown. The objectives of the present study were to evaluate the chronic effects of 2 BZT‐UVs, 2‐(2H‐benzotriazol‐2‐yl)‐4,6‐bis(1‐methyl‐1‐phenylethyl)phenol (UV‐234) and 2‐(2H‐benzotriazol‐2‐yl)‐4,6‐di‐tert‐pentylphenol (UV‐328), on the freshwater green algae Chlamydomonas reinhardtii and the freshwater crustacean Daphnia magna. Organisms were exposed to 0.01 and 10 μg/L of UV‐234, UV‐328, as well as a mixture of the 2 compounds. Life‐history endpoints (viability, reproduction, and growth) and oxidative stress–related biomarkers (gene transcription, reactive oxygen species [ROS] production, and lipid peroxidation) were measured. Daphnia magna growth, reproduction, and gene transcription were not impacted by 21‐d individual or mixed exposure. After 96‐h of exposure, no differences were observed on the cellular viability of C. reinhardtii for either of the 2 BZT‐UVs. In the algae, results showed increased ROS production in response to UV‐328 and lipid peroxidation following exposure to UV‐234. Synergistic effects of the 2 BZT‐UVs were evident at the transcriptional level with 2 to 6 times up‐regulation of glutathione peroxidase (gpx) in response to the mixture for all treatment conditions. The transcription of superoxide dismutase (sod), catalase (cat), and ascorbic peroxidase (apx) was also regulated by UV‐234 and UV‐328 in the green algae, most likely as a result of ROS production and lipid peroxidation. Results from the present study suggest potential impacts of UV‐234 and UV‐328 exposure on the antioxidant defense system in C. reinhardtii. Environ Toxicol Chem 2017;36:3333–3342. © 2017 Crown in the Right of Canada. Published by Wiley Periodicals Inc., on behalf of SETAC.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>28708270</pmid><doi>10.1002/etc.3908</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-4296-146X</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0730-7268
ispartof Environmental toxicology and chemistry, 2017-12, Vol.36 (12), p.3333-3342
issn 0730-7268
1552-8618
language eng
recordid cdi_proquest_journals_1968583714
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Algae
Animals
Antioxidants
Antioxidants - metabolism
Aquatic ecosystems
Aquatic plants
Aquatic toxicology
Ascorbate Peroxidases - metabolism
Benzotriazole
Benzotriazole UV stabilizers
Biodegradation
Biomarkers
Catalase
Catalase - metabolism
Chlamydomonas reinhardtii
Chlamydomonas reinhardtii - drug effects
Chlamydomonas reinhardtii - genetics
Chlorophyta
Chronic effects
Contaminant of emerging concern
Crustaceans
Daphnia - drug effects
Daphnia - genetics
Daphnia - metabolism
Daphnia magna
Exposure
Fresh Water
Freshwater crustaceans
Freshwater invertebrates
Freshwater organisms
Glutathione
Glutathione peroxidase
Glutathione Peroxidase - metabolism
Invertebrates
Life Cycle Stages
Life history
Lipid peroxidation
Lipid Peroxidation - drug effects
Lipids
Oxidative stress
Oxidative Stress - drug effects
Peroxidase
Peroxidation
Phenols
Photochemicals
Reactive oxygen species
Reactive Oxygen Species - metabolism
Reproduction (biology)
Reproduction - drug effects
Shellfish
Superoxide dismutase
Superoxide Dismutase - metabolism
Synergistic effect
Toxicity
Transcription
Transcription, Genetic
Transcriptomics
Triazoles - toxicity
Ultraviolet radiation
Up-Regulation
UV stabilizers
title Transcriptional and cellular effects of benzotriazole UV stabilizers UV‐234 and UV‐328 in the freshwater invertebrates Chlamydomonas reinhardtii and Daphnia magna
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T10%3A43%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Transcriptional%20and%20cellular%20effects%20of%20benzotriazole%20UV%20stabilizers%20UV%E2%80%90234%20and%20UV%E2%80%90328%20in%20the%20freshwater%20invertebrates%20Chlamydomonas%20reinhardtii%20and%20Daphnia%20magna&rft.jtitle=Environmental%20toxicology%20and%20chemistry&rft.au=Giraudo,%20Maeva&rft.date=2017-12&rft.volume=36&rft.issue=12&rft.spage=3333&rft.epage=3342&rft.pages=3333-3342&rft.issn=0730-7268&rft.eissn=1552-8618&rft_id=info:doi/10.1002/etc.3908&rft_dat=%3Cproquest_cross%3E1968583714%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1968583714&rft_id=info:pmid/28708270&rfr_iscdi=true