Toxic effects of nickel oxide bulk and nanoparticles on the aquatic plant Lemna gibba L.
Identifieur interne : 000036 ( PubMed/Curation ); précédent : 000035; suivant : 000037Toxic effects of nickel oxide bulk and nanoparticles on the aquatic plant Lemna gibba L.
Auteurs : Abdallah Oukarroum [Canada] ; Lotfi Barhoumi [Tunisie] ; Mahshid Samadani [Canada] ; David Dewez [Canada]Source :
- BioMed research international [ 2314-6141 ] ; 2015.
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Reactive Oxygen Species.
- chemical , toxicity : Nickel.
- drug effects : Photosynthesis.
- metabolism : Araceae.
- toxicity : Nanoparticles.
- Dose-Response Relationship, Drug.
Abstract
The aquatic plant Lemna gibba L. was used to investigate and compare the toxicity induced by 30 nm nickel oxide nanoparticles (NiO-NPs) and nickel(II) oxide as bulk (NiO-Bulk). Plants were exposed during 24 h to 0-1000 mg/L of NiO-NPs or NiO-Bulk. Analysis of physicochemical characteristics of nanoparticles in solution indicated agglomerations of NiO-NPs in culture medium and a wide size distribution was observed. Both NiO-NPs and NiO-Bulk caused a strong increase in reactive oxygen species (ROS) formation, especially at high concentration (1000 mg/L). These results showed a strong evidence of a cellular oxidative stress induction caused by the exposure to NiO. Under this condition, NiO-NPs and NiO-Bulk induced a strong inhibitory effect on the PSII quantum yield, indicating an alteration of the photosynthetic electron transport performance. Under the experimental conditions used, it is clear that the observed toxicity impact was mainly due to NiO particles effect. Therefore, results of this study permitted determining the use of ROS production as an early biomarker of NiO exposure on the aquatic plant model L. gibba used in toxicity testing.
DOI: 10.1155/2015/501326
PubMed: 26075242
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xml:lang="en"><term>Dose-Response Relationship, Drug</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The aquatic plant Lemna gibba L. was used to investigate and compare the toxicity induced by 30 nm nickel oxide nanoparticles (NiO-NPs) and nickel(II) oxide as bulk (NiO-Bulk). Plants were exposed during 24 h to 0-1000 mg/L of NiO-NPs or NiO-Bulk. Analysis of physicochemical characteristics of nanoparticles in solution indicated agglomerations of NiO-NPs in culture medium and a wide size distribution was observed. Both NiO-NPs and NiO-Bulk caused a strong increase in reactive oxygen species (ROS) formation, especially at high concentration (1000 mg/L). These results showed a strong evidence of a cellular oxidative stress induction caused by the exposure to NiO. Under this condition, NiO-NPs and NiO-Bulk induced a strong inhibitory effect on the PSII quantum yield, indicating an alteration of the photosynthetic electron transport performance. Under the experimental conditions used, it is clear that the observed toxicity impact was mainly due to NiO particles effect. Therefore, results of this study permitted determining the use of ROS production as an early biomarker of NiO exposure on the aquatic plant model L. gibba used in toxicity testing.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">26075242</PMID><DateCreated><Year>2015</Year><Month>06</Month><Day>15</Day></DateCreated><DateCompleted><Year>2016</Year><Month>03</Month><Day>01</Day></DateCompleted><DateRevised><Year>2015</Year><Month>06</Month><Day>17</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">2314-6141</ISSN><JournalIssue CitedMedium="Internet"><Volume>2015</Volume><PubDate><Year>2015</Year></PubDate></JournalIssue><Title>BioMed research international</Title><ISOAbbreviation>Biomed Res Int</ISOAbbreviation></Journal><ArticleTitle>Toxic effects of nickel oxide bulk and nanoparticles on the aquatic plant Lemna gibba L.</ArticleTitle><Pagination><MedlinePgn>501326</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1155/2015/501326</ELocationID><Abstract><AbstractText>The aquatic plant Lemna gibba L. was used to investigate and compare the toxicity induced by 30 nm nickel oxide nanoparticles (NiO-NPs) and nickel(II) oxide as bulk (NiO-Bulk). Plants were exposed during 24 h to 0-1000 mg/L of NiO-NPs or NiO-Bulk. Analysis of physicochemical characteristics of nanoparticles in solution indicated agglomerations of NiO-NPs in culture medium and a wide size distribution was observed. Both NiO-NPs and NiO-Bulk caused a strong increase in reactive oxygen species (ROS) formation, especially at high concentration (1000 mg/L). These results showed a strong evidence of a cellular oxidative stress induction caused by the exposure to NiO. Under this condition, NiO-NPs and NiO-Bulk induced a strong inhibitory effect on the PSII quantum yield, indicating an alteration of the photosynthetic electron transport performance. Under the experimental conditions used, it is clear that the observed toxicity impact was mainly due to NiO particles effect. Therefore, results of this study permitted determining the use of ROS production as an early biomarker of NiO exposure on the aquatic plant model L. gibba used in toxicity testing.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Oukarroum</LastName><ForeName>Abdallah</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Département de Chimie, Université du Québec à Montréal, CP 8888, Succursale Centre-Ville, Montréal, QC, Canada H3C 3P8.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Barhoumi</LastName><ForeName>Lotfi</ForeName><Initials>L</Initials><AffiliationInfo><Affiliation>Faculté des Sciences de Bizerte, Université de Carthage, Jarzouna, 7021 Bizerte, Tunisia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Samadani</LastName><ForeName>Mahshid</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Département de Chimie, Université du Québec à Montréal, CP 8888, Succursale Centre-Ville, Montréal, QC, Canada H3C 3P8.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Dewez</LastName><ForeName>David</ForeName><Initials>D</Initials><Identifier Source="ORCID">0000-0003-4951-9316</Identifier><AffiliationInfo><Affiliation>Département de Chimie, Université du Québec à Montréal, CP 8888, Succursale Centre-Ville, Montréal, QC, Canada H3C 3P8.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2015</Year><Month>05</Month><Day>17</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Biomed Res Int</MedlineTA><NlmUniqueID>101600173</NlmUniqueID></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D017382">Reactive Oxygen Species</NameOfSubstance></Chemical><Chemical><RegistryNumber>7OV03QG267</RegistryNumber><NameOfSubstance UI="D009532">Nickel</NameOfSubstance></Chemical><Chemical><RegistryNumber>C3574QBZ3Y</RegistryNumber><NameOfSubstance UI="C028007">nickel monoxide</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Nanotoxicology. 2014 Jun;8(4):374-82</RefSource><PMID Version="1">23521766</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Environ Toxicol Chem. 2013 Apr;32(4):902-7</RefSource><PMID Version="1">23341248</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Biochim Biophys Acta. 2005 Feb 17;1706(3):250-61</RefSource><PMID Version="1">15694353</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Plant Cell Physiol. 2003 Dec;44(12):1320-9</RefSource><PMID 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