Matches in SemOpenAlex for { <https://semopenalex.org/work/W2012108717> ?p ?o ?g. }
- W2012108717 endingPage "113" @default.
- W2012108717 startingPage "103" @default.
- W2012108717 abstract "In vivo 31P nuclear magnetic resonance spectroscopy (NMR) was used to determine phosphometabolite changes in medaka (Oryzias latipes) during embryogenesis and hypoxia. NMR data were acquired using a flow-through NMR tube perfusion system designed to both deliver oxygenated water to embryos and accommodate a hypoxic challenge. Measurements of embryogenesis at 12- and 24-h intervals throughout 8 days of development (n=3 per time point, 900 embryos per replicate) and during acute hypoxia (n=6, 900 embryos at Iwamatsu stage 37 per replicate) were performed via NMR, and replicate samples (n=4, 250 embryos each) were flash frozen for HPLC analysis. The hypoxic challenge experiment consisted of data acquisition with recirculating water (pre-hypoxic control period; 1 h), without recirculating water (hypoxic challenge; 1 h), then again with recirculating water (recovery period; 1.3 h). Concentrations of ATP, phosphocreatine (PCr), orthophosphate (Pi), phosphomonoesters (PME), phosphodiesters (PDE), and intracellular pH (pHi) were determined by NMR, and ATP, ADP, AMP, GTP, GDP, and PCr were also determined via HPLC. During embryogenesis, [ATP] and [PCr] as determined by HPLC increased from 1-day post fertilization (DPF) levels of 0.93±0.08 and 2.48±0.21 μmol/mg (dry tissue), respectively, to 7.24±0.77 and 15.66±1.08 μmol/mg, respectively, by day 8. [ATP] and [PCr] measured by both NMR and HPLC fluctuated over 1–3 DPF, then increased significantly (p<0.05) over 3–8 DPF, while [PME] and [PDE] decreased (p<0.05) throughout embryogenesis. NMR and HPLC measurements revealed 1–3, 4–5, and 6–8 DPF as periods of embryogenesis significantly different from each other (p<0.05), and representing important transitions in metabolism and growth. During hypoxic challenge, [ATP] and [PCr] declined (p<0.05), [PME] and [PDE] decreased slightly, and [Pi] increased (p<0.05). All phosphometabolites returned to pre-hypoxia concentrations during recovery. The pHi decreased (p<0.05) from 7.10±0.03 to 6.94±0.03 as a result of hypoxia, and failed to return to pre-hypoxic levels within the 1.3-h recovery phase. Results demonstrate the utility of in vivo 31P NMR to detect significant alterations in phosphorylated nucleotides and phosphometabolites at specific developmental stages during medaka development and that late-stage medaka utilize PCr to generate ATP under hypoxic conditions." @default.
- W2012108717 created "2016-06-24" @default.
- W2012108717 creator A5042154436 @default.
- W2012108717 creator A5055330247 @default.
- W2012108717 creator A5055611974 @default.
- W2012108717 creator A5071504404 @default.
- W2012108717 date "2005-01-01" @default.
- W2012108717 modified "2023-09-26" @default.
- W2012108717 title "Metabolic changes in Japanese medaka (Oryzias latipes) during embryogenesis and hypoxia as determined by in vivo 31P NMR" @default.
- W2012108717 cites W1592864469 @default.
- W2012108717 cites W1963554355 @default.
- W2012108717 cites W1974188204 @default.
- W2012108717 cites W1980861344 @default.
- W2012108717 cites W1984750189 @default.
- W2012108717 cites W1984957904 @default.
- W2012108717 cites W1992916753 @default.
- W2012108717 cites W1996290392 @default.
- W2012108717 cites W2003856899 @default.
- W2012108717 cites W2005484211 @default.
- W2012108717 cites W2012315920 @default.
- W2012108717 cites W2012653733 @default.
- W2012108717 cites W2014766558 @default.
- W2012108717 cites W2016254968 @default.
- W2012108717 cites W2016997981 @default.
- W2012108717 cites W2021682846 @default.
- W2012108717 cites W2023497980 @default.
- W2012108717 cites W2026084345 @default.
- W2012108717 cites W2028479043 @default.
- W2012108717 cites W2036009440 @default.
- W2012108717 cites W2050417061 @default.
- W2012108717 cites W2052097318 @default.
- W2012108717 cites W2062425718 @default.
- W2012108717 cites W2063651124 @default.
- W2012108717 cites W2079101363 @default.
- W2012108717 cites W2112645200 @default.
- W2012108717 cites W2119679123 @default.
- W2012108717 cites W2165908005 @default.
- W2012108717 cites W2295525968 @default.
- W2012108717 cites W2525928143 @default.
- W2012108717 cites W4256549147 @default.
- W2012108717 doi "https://doi.org/10.1016/j.cca.2005.01.010" @default.
- W2012108717 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15792629" @default.
- W2012108717 hasPublicationYear "2005" @default.
- W2012108717 type Work @default.
- W2012108717 sameAs 2012108717 @default.
- W2012108717 citedByCount "25" @default.
- W2012108717 countsByYear W20121087172013 @default.
- W2012108717 countsByYear W20121087172017 @default.
- W2012108717 countsByYear W20121087172018 @default.
- W2012108717 countsByYear W20121087172019 @default.
- W2012108717 countsByYear W20121087172020 @default.
- W2012108717 countsByYear W20121087172021 @default.
- W2012108717 countsByYear W20121087172022 @default.
- W2012108717 countsByYear W20121087172023 @default.
- W2012108717 crossrefType "journal-article" @default.
- W2012108717 hasAuthorship W2012108717A5042154436 @default.
- W2012108717 hasAuthorship W2012108717A5055330247 @default.
- W2012108717 hasAuthorship W2012108717A5055611974 @default.
- W2012108717 hasAuthorship W2012108717A5071504404 @default.
- W2012108717 hasConcept C104317684 @default.
- W2012108717 hasConcept C134018914 @default.
- W2012108717 hasConcept C134897140 @default.
- W2012108717 hasConcept C150903083 @default.
- W2012108717 hasConcept C178790620 @default.
- W2012108717 hasConcept C179998833 @default.
- W2012108717 hasConcept C185592680 @default.
- W2012108717 hasConcept C196843134 @default.
- W2012108717 hasConcept C207001950 @default.
- W2012108717 hasConcept C2777132085 @default.
- W2012108717 hasConcept C2777289358 @default.
- W2012108717 hasConcept C2777739839 @default.
- W2012108717 hasConcept C2778626300 @default.
- W2012108717 hasConcept C28406088 @default.
- W2012108717 hasConcept C2986317502 @default.
- W2012108717 hasConcept C2992907065 @default.
- W2012108717 hasConcept C43617362 @default.
- W2012108717 hasConcept C540031477 @default.
- W2012108717 hasConcept C55493867 @default.
- W2012108717 hasConcept C66974803 @default.
- W2012108717 hasConcept C7836513 @default.
- W2012108717 hasConcept C86803240 @default.
- W2012108717 hasConcept C87073359 @default.
- W2012108717 hasConcept C95444343 @default.
- W2012108717 hasConceptScore W2012108717C104317684 @default.
- W2012108717 hasConceptScore W2012108717C134018914 @default.
- W2012108717 hasConceptScore W2012108717C134897140 @default.
- W2012108717 hasConceptScore W2012108717C150903083 @default.
- W2012108717 hasConceptScore W2012108717C178790620 @default.
- W2012108717 hasConceptScore W2012108717C179998833 @default.
- W2012108717 hasConceptScore W2012108717C185592680 @default.
- W2012108717 hasConceptScore W2012108717C196843134 @default.
- W2012108717 hasConceptScore W2012108717C207001950 @default.
- W2012108717 hasConceptScore W2012108717C2777132085 @default.
- W2012108717 hasConceptScore W2012108717C2777289358 @default.
- W2012108717 hasConceptScore W2012108717C2777739839 @default.
- W2012108717 hasConceptScore W2012108717C2778626300 @default.
- W2012108717 hasConceptScore W2012108717C28406088 @default.
- W2012108717 hasConceptScore W2012108717C2986317502 @default.