Matches in SemOpenAlex for { <https://semopenalex.org/work/W2769916410> ?p ?o ?g. }
- W2769916410 endingPage "e0187910" @default.
- W2769916410 startingPage "e0187910" @default.
- W2769916410 abstract "Emerging evidence has suggested that hydrogen sulfide (H2S) may alleviate the cellular damage associated with cerebral ischemia/reperfusion (I/R) injury. In this study, we assessed using 1H-magnetic resonance imaging/magnetic resonance spectroscopy (1H-MRI/MRS) and histologic analysis whether H2S administration prior to reperfusion has neuroprotective effects. We also evaluated for differences in the effects of H2S treatment at 2 time points. 1H-MRI/MRS data were obtained at baseline, and at 3, 9, and 24 h after ischemia from 4 groups: sham, control (I/R injury), sodium hydrosulfide (NaHS)-30 and NaHS-1 (NaHS delivery at 30 and 1 min before reperfusion, respectively). The total infarct volume and the midline shift at 24 h post-ischemia were lowest in the NaHS-1, followed by the NaHS-30 and control groups. Peri-infarct volume was significantly lower in the NaHS-1 compared to NaHS-30 and control animals. The relative apparent diffusion coefficient (ADC) in the peri-infarct region showed that the NaHS-1 group had significantly lower values compared to the NaHS-30 and control animals and that NaHS-1 rats showed significantly higher relative T2 values in the peri-infarct region compared to the controls. The relative ADC value, relative T2 value, levels of N-acetyl-L-aspartate (NAA), and the NAA, glutamate, and taurine combination score (NGT) in the ischemic core region at 24 h post-ischemia did not differ significantly between the 2 NaHS groups and the control except that the NAA and NGT values were higher in the peri-infarct region of the NaHS-1 animals at 9 h post-ischemia. In the ischemic core and peri-infarct regions, the apoptosis rate was lowest in the NaHS-1 group, followed by the NaHS-30 and control groups. Our results suggest that H2S treatment has neuroprotective effects on the peri-infarct region during the evolution of I/R injury. Furthermore, our findings indicate that the administration of H2S immediately prior to reperfusion produces the highest neuroprotective effects." @default.
- W2769916410 created "2017-12-04" @default.
- W2769916410 creator A5001965697 @default.
- W2769916410 creator A5007506402 @default.
- W2769916410 creator A5007870157 @default.
- W2769916410 creator A5017428690 @default.
- W2769916410 creator A5044446885 @default.
- W2769916410 creator A5051616419 @default.
- W2769916410 creator A5052262034 @default.
- W2769916410 creator A5052550275 @default.
- W2769916410 creator A5058382490 @default.
- W2769916410 creator A5061085386 @default.
- W2769916410 creator A5062621324 @default.
- W2769916410 creator A5065271051 @default.
- W2769916410 creator A5071558905 @default.
- W2769916410 creator A5074848763 @default.
- W2769916410 creator A5079680638 @default.
- W2769916410 date "2017-11-21" @default.
- W2769916410 modified "2023-10-16" @default.
- W2769916410 title "The administration of hydrogen sulphide prior to ischemic reperfusion has neuroprotective effects in an acute stroke model" @default.
- W2769916410 cites W1559305991 @default.
- W2769916410 cites W1655344346 @default.
- W2769916410 cites W1850130583 @default.
- W2769916410 cites W1851131104 @default.
- W2769916410 cites W1915513322 @default.
- W2769916410 cites W1964943361 @default.
- W2769916410 cites W1967315370 @default.
- W2769916410 cites W1969827809 @default.
- W2769916410 cites W1971140039 @default.
- W2769916410 cites W1984798596 @default.
- W2769916410 cites W1986569447 @default.
- W2769916410 cites W2004882614 @default.
- W2769916410 cites W2007858244 @default.
- W2769916410 cites W2016293448 @default.
- W2769916410 cites W2035143128 @default.
- W2769916410 cites W2036508025 @default.
- W2769916410 cites W2039618919 @default.
- W2769916410 cites W2042577582 @default.
- W2769916410 cites W2053461574 @default.
- W2769916410 cites W2054064167 @default.
- W2769916410 cites W2069927388 @default.
- W2769916410 cites W2076786048 @default.
- W2769916410 cites W2085364370 @default.
- W2769916410 cites W2102854066 @default.
- W2769916410 cites W2114472543 @default.
- W2769916410 cites W2130415146 @default.
- W2769916410 cites W2144539364 @default.
- W2769916410 cites W2146346910 @default.
- W2769916410 cites W2169746496 @default.
- W2769916410 cites W2218207212 @default.
- W2769916410 cites W2411714162 @default.
- W2769916410 cites W2416132985 @default.
- W2769916410 cites W2520566194 @default.
- W2769916410 cites W2550886340 @default.
- W2769916410 doi "https://doi.org/10.1371/journal.pone.0187910" @default.
- W2769916410 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5697867" @default.
- W2769916410 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29161281" @default.
- W2769916410 hasPublicationYear "2017" @default.
- W2769916410 type Work @default.
- W2769916410 sameAs 2769916410 @default.
- W2769916410 citedByCount "11" @default.
- W2769916410 countsByYear W27699164102018 @default.
- W2769916410 countsByYear W27699164102019 @default.
- W2769916410 countsByYear W27699164102020 @default.
- W2769916410 countsByYear W27699164102021 @default.
- W2769916410 countsByYear W27699164102023 @default.
- W2769916410 crossrefType "journal-article" @default.
- W2769916410 hasAuthorship W2769916410A5001965697 @default.
- W2769916410 hasAuthorship W2769916410A5007506402 @default.
- W2769916410 hasAuthorship W2769916410A5007870157 @default.
- W2769916410 hasAuthorship W2769916410A5017428690 @default.
- W2769916410 hasAuthorship W2769916410A5044446885 @default.
- W2769916410 hasAuthorship W2769916410A5051616419 @default.
- W2769916410 hasAuthorship W2769916410A5052262034 @default.
- W2769916410 hasAuthorship W2769916410A5052550275 @default.
- W2769916410 hasAuthorship W2769916410A5058382490 @default.
- W2769916410 hasAuthorship W2769916410A5061085386 @default.
- W2769916410 hasAuthorship W2769916410A5062621324 @default.
- W2769916410 hasAuthorship W2769916410A5065271051 @default.
- W2769916410 hasAuthorship W2769916410A5071558905 @default.
- W2769916410 hasAuthorship W2769916410A5074848763 @default.
- W2769916410 hasAuthorship W2769916410A5079680638 @default.
- W2769916410 hasBestOaLocation W27699164101 @default.
- W2769916410 hasConcept C126322002 @default.
- W2769916410 hasConcept C126838900 @default.
- W2769916410 hasConcept C143409427 @default.
- W2769916410 hasConcept C164705383 @default.
- W2769916410 hasConcept C170493617 @default.
- W2769916410 hasConcept C178790620 @default.
- W2769916410 hasConcept C185592680 @default.
- W2769916410 hasConcept C25498285 @default.
- W2769916410 hasConcept C2779701627 @default.
- W2769916410 hasConcept C2780114680 @default.
- W2769916410 hasConcept C2780519940 @default.
- W2769916410 hasConcept C2780564542 @default.
- W2769916410 hasConcept C42219234 @default.
- W2769916410 hasConcept C515207424 @default.
- W2769916410 hasConcept C518881349 @default.