In Vivo Evaluation of Radiofluorinated Caspase-3/7 Inhibitors as Radiotracers for Apoptosis Imaging and Comparison with [18F]ML-10 in a Stroke Model in the Rat.
Identifieur interne : 002251 ( PubMed/Curation ); précédent : 002250; suivant : 002252In Vivo Evaluation of Radiofluorinated Caspase-3/7 Inhibitors as Radiotracers for Apoptosis Imaging and Comparison with [18F]ML-10 in a Stroke Model in the Rat.
Auteurs : Marie Médoc [France] ; Martine Dhilly [France] ; Lidia Matesic [Australie] ; Jérôme Toutain [France] ; Anwen M. Krause-Heuer [Australie] ; Jérôme Delamare [France] ; Benjamin H. Fraser [Australie] ; Omar Touzani [France] ; Louisa Barré [France] ; Ivan Greguric [Australie] ; Franck Sobrio [France]Source :
- Molecular imaging and biology : MIB : the official publication of the Academy of Molecular Imaging [ 1860-2002 ] ; 2016.
Descripteurs français
- KwdFr :
- Accident vasculaire cérébral (anatomopathologie), Accident vasculaire cérébral (imagerie diagnostique), Acide méthyl-malonique (analogues et dérivés), Acide méthyl-malonique (pharmacocinétique), Acide méthyl-malonique (pharmacologie), Animaux, Apoptose (), Caspase-3 (métabolisme), Caspase-7 (métabolisme), Imagerie moléculaire (), Inhibiteurs des caspases (pharmacocinétique), Inhibiteurs des caspases (pharmacologie), Inhibiteurs des caspases (sang), Isatine (), Isatine (pharmacologie), Modèles animaux de maladie humaine, Mâle, Radiopharmaceutiques (pharmacocinétique), Radiopharmaceutiques (pharmacologie), Radiopharmaceutiques (sang), Rat Sprague-Dawley, Répartition dans les tissus (), Scintigraphie.
- MESH :
- analogues et dérivés : Acide méthyl-malonique.
- anatomopathologie : Accident vasculaire cérébral.
- imagerie diagnostique : Accident vasculaire cérébral.
- métabolisme : Caspase-3, Caspase-7.
- pharmacocinétique : Acide méthyl-malonique, Inhibiteurs des caspases, Radiopharmaceutiques.
- pharmacologie : Acide méthyl-malonique, Inhibiteurs des caspases, Isatine, Radiopharmaceutiques.
- sang : Inhibiteurs des caspases, Radiopharmaceutiques.
- Animaux, Apoptose, Imagerie moléculaire, Isatine, Modèles animaux de maladie humaine, Mâle, Rat Sprague-Dawley, Répartition dans les tissus, Scintigraphie.
English descriptors
- KwdEn :
- Animals, Apoptosis (drug effects), Caspase 3 (metabolism), Caspase 7 (metabolism), Caspase Inhibitors (blood), Caspase Inhibitors (pharmacokinetics), Caspase Inhibitors (pharmacology), Disease Models, Animal, Isatin (chemistry), Isatin (pharmacology), Male, Methylmalonic Acid (analogs & derivatives), Methylmalonic Acid (pharmacokinetics), Methylmalonic Acid (pharmacology), Molecular Imaging (methods), Radionuclide Imaging, Radiopharmaceuticals (blood), Radiopharmaceuticals (pharmacokinetics), Radiopharmaceuticals (pharmacology), Rats, Sprague-Dawley, Stroke (diagnostic imaging), Stroke (pathology), Tissue Distribution (drug effects).
- MESH :
- chemical , analogs & derivatives : Methylmalonic Acid.
- chemical , blood : Caspase Inhibitors, Radiopharmaceuticals.
- chemical , chemistry : Isatin.
- chemical , metabolism : Caspase 3, Caspase 7.
- diagnostic imaging : Stroke.
- drug effects : Apoptosis, Tissue Distribution.
- methods : Molecular Imaging.
- pathology : Stroke.
- chemical , pharmacokinetics : Caspase Inhibitors, Methylmalonic Acid, Radiopharmaceuticals.
- chemical , pharmacology : Caspase Inhibitors, Isatin, Methylmalonic Acid, Radiopharmaceuticals.
- Animals, Disease Models, Animal, Male, Radionuclide Imaging, Rats, Sprague-Dawley.
Abstract
The first biological evaluation of two potent fluorine-18 radiolabelled inhibitors of caspase-3/7 was achieved in a cerebral stroke rat model to visualize apoptosis.
DOI: 10.1007/s11307-015-0865-1
PubMed: 26013478
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<term>Apoptosis (drug effects)</term>
<term>Caspase 3 (metabolism)</term>
<term>Caspase 7 (metabolism)</term>
<term>Caspase Inhibitors (blood)</term>
<term>Caspase Inhibitors (pharmacokinetics)</term>
<term>Caspase Inhibitors (pharmacology)</term>
<term>Disease Models, Animal</term>
<term>Isatin (chemistry)</term>
<term>Isatin (pharmacology)</term>
<term>Male</term>
<term>Methylmalonic Acid (analogs & derivatives)</term>
<term>Methylmalonic Acid (pharmacokinetics)</term>
<term>Methylmalonic Acid (pharmacology)</term>
<term>Molecular Imaging (methods)</term>
<term>Radionuclide Imaging</term>
<term>Radiopharmaceuticals (blood)</term>
<term>Radiopharmaceuticals (pharmacokinetics)</term>
<term>Radiopharmaceuticals (pharmacology)</term>
<term>Rats, Sprague-Dawley</term>
<term>Stroke (diagnostic imaging)</term>
<term>Stroke (pathology)</term>
<term>Tissue Distribution (drug effects)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Accident vasculaire cérébral (anatomopathologie)</term>
<term>Accident vasculaire cérébral (imagerie diagnostique)</term>
<term>Acide méthyl-malonique (analogues et dérivés)</term>
<term>Acide méthyl-malonique (pharmacocinétique)</term>
<term>Acide méthyl-malonique (pharmacologie)</term>
<term>Animaux</term>
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<term>Caspase-3 (métabolisme)</term>
<term>Caspase-7 (métabolisme)</term>
<term>Imagerie moléculaire ()</term>
<term>Inhibiteurs des caspases (pharmacocinétique)</term>
<term>Inhibiteurs des caspases (pharmacologie)</term>
<term>Inhibiteurs des caspases (sang)</term>
<term>Isatine ()</term>
<term>Isatine (pharmacologie)</term>
<term>Modèles animaux de maladie humaine</term>
<term>Mâle</term>
<term>Radiopharmaceutiques (pharmacocinétique)</term>
<term>Radiopharmaceutiques (pharmacologie)</term>
<term>Radiopharmaceutiques (sang)</term>
<term>Rat Sprague-Dawley</term>
<term>Répartition dans les tissus ()</term>
<term>Scintigraphie</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analogs & derivatives" xml:lang="en"><term>Methylmalonic Acid</term>
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</keywords>
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<term>Caspase 7</term>
</keywords>
<keywords scheme="MESH" qualifier="analogues et dérivés" xml:lang="fr"><term>Acide méthyl-malonique</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Accident vasculaire cérébral</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Stroke</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Apoptosis</term>
<term>Tissue Distribution</term>
</keywords>
<keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr"><term>Accident vasculaire cérébral</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Molecular Imaging</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Caspase-3</term>
<term>Caspase-7</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Stroke</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacocinétique" xml:lang="fr"><term>Acide méthyl-malonique</term>
<term>Inhibiteurs des caspases</term>
<term>Radiopharmaceutiques</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacokinetics" xml:lang="en"><term>Caspase Inhibitors</term>
<term>Methylmalonic Acid</term>
<term>Radiopharmaceuticals</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Acide méthyl-malonique</term>
<term>Inhibiteurs des caspases</term>
<term>Isatine</term>
<term>Radiopharmaceutiques</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Caspase Inhibitors</term>
<term>Isatin</term>
<term>Methylmalonic Acid</term>
<term>Radiopharmaceuticals</term>
</keywords>
<keywords scheme="MESH" qualifier="sang" xml:lang="fr"><term>Inhibiteurs des caspases</term>
<term>Radiopharmaceutiques</term>
</keywords>
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<term>Disease Models, Animal</term>
<term>Male</term>
<term>Radionuclide Imaging</term>
<term>Rats, Sprague-Dawley</term>
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<term>Apoptose</term>
<term>Imagerie moléculaire</term>
<term>Isatine</term>
<term>Modèles animaux de maladie humaine</term>
<term>Mâle</term>
<term>Rat Sprague-Dawley</term>
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<front><div type="abstract" xml:lang="en">The first biological evaluation of two potent fluorine-18 radiolabelled inhibitors of caspase-3/7 was achieved in a cerebral stroke rat model to visualize apoptosis.</div>
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<DateCreated><Year>2016</Year>
<Month>01</Month>
<Day>22</Day>
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<DateCompleted><Year>2016</Year>
<Month>10</Month>
<Day>14</Day>
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<Month>11</Month>
<Day>02</Day>
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<Title>Molecular imaging and biology : MIB : the official publication of the Academy of Molecular Imaging</Title>
<ISOAbbreviation>Mol Imaging Biol</ISOAbbreviation>
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<ArticleTitle>In Vivo Evaluation of Radiofluorinated Caspase-3/7 Inhibitors as Radiotracers for Apoptosis Imaging and Comparison with [18F]ML-10 in a Stroke Model in the Rat.</ArticleTitle>
<Pagination><MedlinePgn>117-26</MedlinePgn>
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<Abstract><AbstractText Label="PURPOSE" NlmCategory="OBJECTIVE">The first biological evaluation of two potent fluorine-18 radiolabelled inhibitors of caspase-3/7 was achieved in a cerebral stroke rat model to visualize apoptosis.</AbstractText>
<AbstractText Label="PROCEDURES" NlmCategory="METHODS">In vivo characteristics of isatins [(18)F]-2 and [(18)F]-3 were studied and compared by μPET to previously described 1-[4-(2-[(18)F]fluoroethyl)benzyl]-5-(2-methoxymethylpyrrolidin-1-ylsulfonyl)isatin ([(18)F]-1) and to 2-(5-[(18)F]fluoropentyl)-2-methyl-malonic acid ([(18)F]ML-10) used as a reference radiotracer in a rat stroke model.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">[(18)F]-2 and [(18)F]-3 were radiolabelled with high radiochemical purity and high specific radioactivity. Radioactivity uptakes in ischemic and contralateral brain regions were weak for the three radiolabelled isatins and lower for [(18)F]ML-10. In μPET, time activity curves showed significant uptake differences between both regions of interest for [(18)F]-1 after 45 min. No differences were observed for [(18)F]ML-10.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Radiolabelled isatins are more promising radiotracers to image apoptosis than [(18)F]ML-10 in this stroke animal model without craniectomy. In particular, [(18)F]-1 presented significant uptake in apoptotic area 45 min after administration.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Médoc</LastName>
<ForeName>Marie</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>CEA, I2BM, LDM-TEP, UMR 6301 ISTCT, GIP Cyceron, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>CNRS, UMR 6301 ISTCT, GIP Cyceron, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Université de Caen Basse-Normandie, UMR 6301 ISTCT, GIP Cyceron, BP 5229, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Dhilly</LastName>
<ForeName>Martine</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>CEA, I2BM, LDM-TEP, UMR 6301 ISTCT, GIP Cyceron, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>CNRS, UMR 6301 ISTCT, GIP Cyceron, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Université de Caen Basse-Normandie, UMR 6301 ISTCT, GIP Cyceron, BP 5229, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Matesic</LastName>
<ForeName>Lidia</ForeName>
<Initials>L</Initials>
<AffiliationInfo><Affiliation>Life Sciences Division, Australian Nuclear Science and Technology Organisation, Kirrawee DC, NSW, 2232, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Toutain</LastName>
<ForeName>Jérôme</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>CNRS, UMR 6301 ISTCT, GIP Cyceron, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Université de Caen Basse-Normandie, UMR 6301 ISTCT, GIP Cyceron, BP 5229, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Krause-Heuer</LastName>
<ForeName>Anwen M</ForeName>
<Initials>AM</Initials>
<AffiliationInfo><Affiliation>Life Sciences Division, Australian Nuclear Science and Technology Organisation, Kirrawee DC, NSW, 2232, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Delamare</LastName>
<ForeName>Jérôme</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>CEA, I2BM, LDM-TEP, UMR 6301 ISTCT, GIP Cyceron, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>CNRS, UMR 6301 ISTCT, GIP Cyceron, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Université de Caen Basse-Normandie, UMR 6301 ISTCT, GIP Cyceron, BP 5229, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Fraser</LastName>
<ForeName>Benjamin H</ForeName>
<Initials>BH</Initials>
<AffiliationInfo><Affiliation>Life Sciences Division, Australian Nuclear Science and Technology Organisation, Kirrawee DC, NSW, 2232, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Touzani</LastName>
<ForeName>Omar</ForeName>
<Initials>O</Initials>
<AffiliationInfo><Affiliation>CNRS, UMR 6301 ISTCT, GIP Cyceron, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Université de Caen Basse-Normandie, UMR 6301 ISTCT, GIP Cyceron, BP 5229, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Barré</LastName>
<ForeName>Louisa</ForeName>
<Initials>L</Initials>
<AffiliationInfo><Affiliation>CEA, I2BM, LDM-TEP, UMR 6301 ISTCT, GIP Cyceron, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>CNRS, UMR 6301 ISTCT, GIP Cyceron, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Université de Caen Basse-Normandie, UMR 6301 ISTCT, GIP Cyceron, BP 5229, F-14074, Caen, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Greguric</LastName>
<ForeName>Ivan</ForeName>
<Initials>I</Initials>
<AffiliationInfo><Affiliation>Life Sciences Division, Australian Nuclear Science and Technology Organisation, Kirrawee DC, NSW, 2232, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Sobrio</LastName>
<ForeName>Franck</ForeName>
<Initials>F</Initials>
<AffiliationInfo><Affiliation>CEA, I2BM, LDM-TEP, UMR 6301 ISTCT, GIP Cyceron, F-14074, Caen, France. sobrio@cyceron.fr.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>CNRS, UMR 6301 ISTCT, GIP Cyceron, F-14074, Caen, France. sobrio@cyceron.fr.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Université de Caen Basse-Normandie, UMR 6301 ISTCT, GIP Cyceron, BP 5229, F-14074, Caen, France. sobrio@cyceron.fr.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Mol Imaging Biol</MedlineTA>
<NlmUniqueID>101125610</NlmUniqueID>
<ISSNLinking>1536-1632</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C532430">5-fluoropentyl-2-methylmalonic acid</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D061945">Caspase Inhibitors</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D019275">Radiopharmaceuticals</NameOfSubstance>
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<Chemical><RegistryNumber>82X95S7M06</RegistryNumber>
<NameOfSubstance UI="D007510">Isatin</NameOfSubstance>
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<Chemical><RegistryNumber>8LL8S712J7</RegistryNumber>
<NameOfSubstance UI="D008764">Methylmalonic Acid</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 3.4.22.-</RegistryNumber>
<NameOfSubstance UI="D053148">Caspase 3</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 3.4.22.-</RegistryNumber>
<NameOfSubstance UI="D053179">Caspase 7</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017209" MajorTopicYN="N">Apoptosis</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D053148" MajorTopicYN="N">Caspase 3</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D053179" MajorTopicYN="N">Caspase 7</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D061945" MajorTopicYN="N">Caspase Inhibitors</DescriptorName>
<QualifierName UI="Q000097" MajorTopicYN="N">blood</QualifierName>
<QualifierName UI="Q000493" MajorTopicYN="N">pharmacokinetics</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004195" MajorTopicYN="N">Disease Models, Animal</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007510" MajorTopicYN="N">Isatin</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008764" MajorTopicYN="N">Methylmalonic Acid</DescriptorName>
<QualifierName UI="Q000031" MajorTopicYN="Y">analogs & derivatives</QualifierName>
<QualifierName UI="Q000493" MajorTopicYN="N">pharmacokinetics</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D057054" MajorTopicYN="N">Molecular Imaging</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011877" MajorTopicYN="N">Radionuclide Imaging</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D019275" MajorTopicYN="N">Radiopharmaceuticals</DescriptorName>
<QualifierName UI="Q000097" MajorTopicYN="N">blood</QualifierName>
<QualifierName UI="Q000493" MajorTopicYN="N">pharmacokinetics</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017207" MajorTopicYN="N">Rats, Sprague-Dawley</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D020521" MajorTopicYN="N">Stroke</DescriptorName>
<QualifierName UI="Q000000981" MajorTopicYN="Y">diagnostic imaging</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014018" MajorTopicYN="N">Tissue Distribution</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Apoptosis</Keyword>
<Keyword MajorTopicYN="N">Caspase-3 inhibitors</Keyword>
<Keyword MajorTopicYN="N">Cerebral stroke</Keyword>
<Keyword MajorTopicYN="N">Fluorine-18</Keyword>
<Keyword MajorTopicYN="N">In vivo evaluation</Keyword>
<Keyword MajorTopicYN="N">Isatins</Keyword>
<Keyword MajorTopicYN="N">Ischemia</Keyword>
<Keyword MajorTopicYN="N">PET</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2015</Year>
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<Day>28</Day>
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<Month>5</Month>
<Day>28</Day>
<Hour>6</Hour>
<Minute>0</Minute>
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<PubMedPubDate PubStatus="medline"><Year>2016</Year>
<Month>10</Month>
<Day>16</Day>
<Hour>6</Hour>
<Minute>0</Minute>
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<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">26013478</ArticleId>
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