Retinal metabolic events in preconditioning light stress as revealed by wide-spectrum targeted metabolomics.
Identifieur interne : 001278 ( PubMed/Curation ); précédent : 001277; suivant : 001279Retinal metabolic events in preconditioning light stress as revealed by wide-spectrum targeted metabolomics.
Auteurs : Juan Manuel Chao De La Barca [France] ; Nuan-Ting Huang ; Haihan Jiao ; Lydie Tessier [France] ; Cédric Gadras [France] ; Gilles Simard [France] ; Riccardo Natoli ; Guillaume Tcherkez ; Pascal Reynier [France] ; Krisztina ValterSource :
- Metabolomics : Official journal of the Metabolomic Society [ 1573-3882 ] ; 2017.
Abstract
Light is the primary stimulus for vision, but may also cause damage to the retina. Pre-exposing the retina to sub-lethal amount of light (or preconditioning) improves chances for retinal cells to survive acute damaging light stress.
DOI: 10.1007/s11306-016-1156-9
PubMed: 28706468
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Nuan-Ting Huang<affiliation><nlm:affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</nlm:affiliation><wicri:noCountry code="subField">ACT 2601 Australia</wicri:noCountry></affiliation><affiliation><nlm:affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</nlm:affiliation><wicri:noCountry code="subField">ACT 2601 Australia</wicri:noCountry></affiliation><affiliation><nlm:affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</nlm:affiliation><wicri:noCountry code="subField">ACT 2601 Australia</wicri:noCountry></affiliation><affiliation><nlm:affiliation>Research School of Biology, College of Medicine, Biology and Environment, Australian National University, Canberra, ACT 2601 Australia.</nlm:affiliation><wicri:noCountry code="subField">ACT 2601 Australia</wicri:noCountry></affiliation><affiliation><nlm:affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</nlm:affiliation><wicri:noCountry code="subField">ACT 2601 Australia</wicri:noCountry></affiliation>Le document en format XML
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code="subField">ACT 2601 Australia</wicri:noCountry></affiliation></author><author><name sortKey="Reynier, Pascal" sort="Reynier, Pascal" uniqKey="Reynier P" first="Pascal" last="Reynier">Pascal Reynier</name><affiliation wicri:level="1"><nlm:affiliation>PREMMi/Pôle de Recherche et d'Enseignement en Médecine Mitochondriale, Institut MITOVASC, CNRS 6214, INSERM U1083, Université d'Angers, 49933 Angers, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>PREMMi/Pôle de Recherche et d'Enseignement en Médecine Mitochondriale, Institut MITOVASC, CNRS 6214, INSERM U1083, Université d'Angers, 49933 Angers</wicri:regionArea></affiliation></author><author><name sortKey="Valter, Krisztina" sort="Valter, Krisztina" uniqKey="Valter K" first="Krisztina" last="Valter">Krisztina Valter</name><affiliation><nlm:affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</nlm:affiliation><wicri:noCountry code="subField">ACT 2601 Australia</wicri:noCountry></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2017">2017</date><idno type="RBID">pubmed:28706468</idno><idno type="pmid">28706468</idno><idno type="doi">10.1007/s11306-016-1156-9</idno><idno type="wicri:Area/PubMed/Corpus">001293</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">001293</idno><idno type="wicri:Area/PubMed/Curation">001278</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">001278</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Retinal metabolic events in preconditioning light stress as revealed by wide-spectrum targeted metabolomics.</title><author><name sortKey="De La Barca, Juan Manuel Chao" sort="De La Barca, Juan Manuel Chao" uniqKey="De La Barca J" first="Juan Manuel Chao" last="De La Barca">Juan Manuel Chao De La Barca</name><affiliation wicri:level="1"><nlm:affiliation>PREMMi/Pôle de Recherche et d'Enseignement en Médecine Mitochondriale, Institut MITOVASC, CNRS 6214, INSERM U1083, Université d'Angers, 49933 Angers, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>PREMMi/Pôle de Recherche et d'Enseignement en Médecine Mitochondriale, Institut MITOVASC, CNRS 6214, INSERM U1083, Université d'Angers, 49933 Angers</wicri:regionArea></affiliation></author><author><name sortKey="Huang, Nuan Ting" sort="Huang, Nuan Ting" uniqKey="Huang N" first="Nuan-Ting" last="Huang">Nuan-Ting Huang</name><affiliation><nlm:affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</nlm:affiliation><wicri:noCountry code="subField">ACT 2601 Australia</wicri:noCountry></affiliation></author><author><name sortKey="Jiao, Haihan" sort="Jiao, Haihan" uniqKey="Jiao H" first="Haihan" last="Jiao">Haihan Jiao</name><affiliation><nlm:affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</nlm:affiliation><wicri:noCountry code="subField">ACT 2601 Australia</wicri:noCountry></affiliation></author><author><name sortKey="Tessier, Lydie" sort="Tessier, Lydie" uniqKey="Tessier L" first="Lydie" last="Tessier">Lydie Tessier</name><affiliation wicri:level="1"><nlm:affiliation>Département de Biochimie et Génétique, Centre Hospitalier Universitaire, 4 rue Larrey, 49933 Angers cedex 9, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>Département de Biochimie et Génétique, Centre Hospitalier Universitaire, 4 rue Larrey, 49933 Angers cedex 9</wicri:regionArea></affiliation></author><author><name sortKey="Gadras, Cedric" sort="Gadras, Cedric" uniqKey="Gadras C" first="Cédric" last="Gadras">Cédric Gadras</name><affiliation wicri:level="1"><nlm:affiliation>Département de Biochimie et Génétique, Centre Hospitalier Universitaire, 4 rue Larrey, 49933 Angers cedex 9, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>Département de Biochimie et Génétique, Centre Hospitalier Universitaire, 4 rue Larrey, 49933 Angers cedex 9</wicri:regionArea></affiliation></author><author><name sortKey="Simard, Gilles" sort="Simard, Gilles" uniqKey="Simard G" first="Gilles" last="Simard">Gilles Simard</name><affiliation wicri:level="1"><nlm:affiliation>Département de Biochimie et Génétique, Centre Hospitalier Universitaire, 4 rue Larrey, 49933 Angers cedex 9, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>Département de Biochimie et Génétique, Centre Hospitalier Universitaire, 4 rue Larrey, 49933 Angers cedex 9</wicri:regionArea></affiliation></author><author><name sortKey="Natoli, Riccardo" sort="Natoli, Riccardo" uniqKey="Natoli R" first="Riccardo" last="Natoli">Riccardo Natoli</name><affiliation><nlm:affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</nlm:affiliation><wicri:noCountry code="subField">ACT 2601 Australia</wicri:noCountry></affiliation></author><author><name sortKey="Tcherkez, Guillaume" sort="Tcherkez, Guillaume" uniqKey="Tcherkez G" first="Guillaume" last="Tcherkez">Guillaume Tcherkez</name><affiliation><nlm:affiliation>Research School of Biology, College of Medicine, Biology and Environment, Australian National University, Canberra, ACT 2601 Australia.</nlm:affiliation><wicri:noCountry code="subField">ACT 2601 Australia</wicri:noCountry></affiliation></author><author><name sortKey="Reynier, Pascal" sort="Reynier, Pascal" uniqKey="Reynier P" first="Pascal" last="Reynier">Pascal Reynier</name><affiliation wicri:level="1"><nlm:affiliation>PREMMi/Pôle de Recherche et d'Enseignement en Médecine Mitochondriale, Institut MITOVASC, CNRS 6214, INSERM U1083, Université d'Angers, 49933 Angers, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>PREMMi/Pôle de Recherche et d'Enseignement en Médecine Mitochondriale, Institut MITOVASC, CNRS 6214, INSERM U1083, Université d'Angers, 49933 Angers</wicri:regionArea></affiliation></author><author><name sortKey="Valter, Krisztina" sort="Valter, Krisztina" uniqKey="Valter K" first="Krisztina" last="Valter">Krisztina Valter</name><affiliation><nlm:affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</nlm:affiliation><wicri:noCountry code="subField">ACT 2601 Australia</wicri:noCountry></affiliation></author></analytic><series><title level="j">Metabolomics : Official journal of the Metabolomic Society</title><idno type="ISSN">1573-3882</idno><imprint><date when="2017" type="published">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Light is the primary stimulus for vision, but may also cause damage to the retina. Pre-exposing the retina to sub-lethal amount of light (or preconditioning) improves chances for retinal cells to survive acute damaging light stress.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">28706468</PMID><DateCreated><Year>2017</Year><Month>07</Month><Day>14</Day></DateCreated><DateRevised><Year>2017</Year><Month>10</Month><Day>25</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">1573-3882</ISSN><JournalIssue CitedMedium="Print"><Volume>13</Volume><Issue>3</Issue><PubDate><Year>2017</Year></PubDate></JournalIssue><Title>Metabolomics : Official journal of the Metabolomic Society</Title><ISOAbbreviation>Metabolomics</ISOAbbreviation></Journal><ArticleTitle>Retinal metabolic events in preconditioning light stress as revealed by wide-spectrum targeted metabolomics.</ArticleTitle><Pagination><MedlinePgn>22</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1007/s11306-016-1156-9</ELocationID><Abstract><AbstractText Label="INTRODUCTION" NlmCategory="BACKGROUND">Light is the primary stimulus for vision, but may also cause damage to the retina. Pre-exposing the retina to sub-lethal amount of light (or preconditioning) improves chances for retinal cells to survive acute damaging light stress.</AbstractText><AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">This study aims at exploring the changes in retinal metabolome after mild light stress and identifying mechanisms that may be involved in preconditioning.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">Retinas from 12 rats exposed to mild light stress (1000 lux × for 12 h) and 12 controls were collected one and seven days after light stress (LS). One retina was used for targeted metabolomics analysis using the Biocrates p180 kit while the fellow retina was used for histological and immunohistochemistry analysis.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">Immunohistochemistry confirmed that in this experiment, a mild LS with retinal immune response and minimal photoreceptor loss occurred. Compared to controls, LS induced an increased concentration in phosphatidylcholines. The concentration in some amino acids and biogenic amines, particularly those related to the nitric oxide pathway (like asymmetric dimethylarginine (ADMA), arginine and citrulline) also increased 1 day after LS. 7 days after LS, the concentration in two sphingomyelins and phenylethylamine was found to be higher. We further found that in controls, retina metabolome was different between males and females: male retinas had an increased concentration in tyrosine, acetyl-ornithine, phosphatidylcholines and (acyl)-carnitines.</AbstractText><AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Besides retinal sexual metabolic dimorphism, this study shows that preconditioning is mostly associated with re-organisation of lipid metabolism and changes in amino acid composition, likely reflecting the involvement of arginine-dependent NO signalling.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>de la Barca</LastName><ForeName>Juan Manuel Chao</ForeName><Initials>JMC</Initials><AffiliationInfo><Affiliation>PREMMi/Pôle de Recherche et d'Enseignement en Médecine Mitochondriale, Institut MITOVASC, CNRS 6214, INSERM U1083, Université d'Angers, 49933 Angers, France.</Affiliation><Identifier Source="GRID">grid.7252.2</Identifier><Identifier Source="ISNI">0000000122483363</Identifier></AffiliationInfo><AffiliationInfo><Affiliation>Département de Biochimie et Génétique, Centre Hospitalier Universitaire, 4 rue Larrey, 49933 Angers cedex 9, France.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</Affiliation><Identifier Source="GRID">grid.1001.0</Identifier><Identifier Source="ISNI">0000000121807477</Identifier></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Huang</LastName><ForeName>Nuan-Ting</ForeName><Initials>NT</Initials><AffiliationInfo><Affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</Affiliation><Identifier Source="GRID">grid.1001.0</Identifier><Identifier Source="ISNI">0000000121807477</Identifier></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Jiao</LastName><ForeName>Haihan</ForeName><Initials>H</Initials><AffiliationInfo><Affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</Affiliation><Identifier Source="GRID">grid.1001.0</Identifier><Identifier Source="ISNI">0000000121807477</Identifier></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Tessier</LastName><ForeName>Lydie</ForeName><Initials>L</Initials><AffiliationInfo><Affiliation>Département de Biochimie et Génétique, Centre Hospitalier Universitaire, 4 rue Larrey, 49933 Angers cedex 9, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Gadras</LastName><ForeName>Cédric</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>Département de Biochimie et Génétique, Centre Hospitalier Universitaire, 4 rue Larrey, 49933 Angers cedex 9, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Simard</LastName><ForeName>Gilles</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>Département de Biochimie et Génétique, Centre Hospitalier Universitaire, 4 rue Larrey, 49933 Angers cedex 9, France.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>INSERM U1063, Université d'Angers, 49933 Angers, France.</Affiliation><Identifier Source="GRID">grid.7252.2</Identifier><Identifier Source="ISNI">0000000122483363</Identifier></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Natoli</LastName><ForeName>Riccardo</ForeName><Initials>R</Initials><AffiliationInfo><Affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</Affiliation><Identifier Source="GRID">grid.1001.0</Identifier><Identifier Source="ISNI">0000000121807477</Identifier></AffiliationInfo><AffiliationInfo><Affiliation>Medical School, Australian National University, Canberra, ACT 2601 Australia.</Affiliation><Identifier Source="GRID">grid.1001.0</Identifier><Identifier Source="ISNI">0000000121807477</Identifier></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Tcherkez</LastName><ForeName>Guillaume</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>Research School of Biology, College of Medicine, Biology and Environment, Australian National University, Canberra, ACT 2601 Australia.</Affiliation><Identifier Source="GRID">grid.1001.0</Identifier><Identifier Source="ISNI">0000000121807477</Identifier></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Reynier</LastName><ForeName>Pascal</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>PREMMi/Pôle de Recherche et d'Enseignement en Médecine Mitochondriale, Institut MITOVASC, CNRS 6214, INSERM U1083, Université d'Angers, 49933 Angers, France.</Affiliation><Identifier Source="GRID">grid.7252.2</Identifier><Identifier Source="ISNI">0000000122483363</Identifier></AffiliationInfo><AffiliationInfo><Affiliation>Département de Biochimie et Génétique, Centre Hospitalier Universitaire, 4 rue Larrey, 49933 Angers cedex 9, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Valter</LastName><ForeName>Krisztina</ForeName><Initials>K</Initials><AffiliationInfo><Affiliation>Eccles Institute of Neuroscience, John Curtin School of Medical research, Australian National University, Canberra, ACT 2601 Australia.</Affiliation><Identifier Source="GRID">grid.1001.0</Identifier><Identifier Source="ISNI">0000000121807477</Identifier></AffiliationInfo><AffiliationInfo><Affiliation>Medical School, Australian National University, Canberra, ACT 2601 Australia.</Affiliation><Identifier Source="GRID">grid.1001.0</Identifier><Identifier Source="ISNI">0000000121807477</Identifier></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>R01 EY004367</GrantID><Acronym>EY</Acronym><Agency>NEI NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2017</Year><Month>01</Month><Day>20</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Metabolomics</MedlineTA><NlmUniqueID>101274889</NlmUniqueID><ISSNLinking>1573-3882</ISSNLinking></MedlineJournalInfo><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Invest Ophthalmol. 1966 Oct;5(5):450-73</RefSource><PMID Version="1">5929286</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Exp Eye Res. 2001 Oct;73(4):569-77</RefSource><PMID Version="1">11825027</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Prog Retin Eye Res. 2007 May;26(3):205-38</RefSource><PMID 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PubStatus="accepted"><Year>2016</Year><Month>12</Month><Day>20</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2017</Year><Month>7</Month><Day>15</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2017</Year><Month>7</Month><Day>15</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2017</Year><Month>7</Month><Day>15</Day><Hour>6</Hour><Minute>1</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">28706468</ArticleId><ArticleId IdType="doi">10.1007/s11306-016-1156-9</ArticleId><ArticleId IdType="pii">1156</ArticleId><ArticleId IdType="pmc">PMC5486622</ArticleId></ArticleIdList><pmc-dir>pmcsd</pmc-dir>
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