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- W3198210902 abstract "Naked mole-rats (NMRs; Heterocephalus glaber) are among the most hypoxia-tolerant mammals. There is evidence that the NMR brain tolerates in vitro hypoxia and NMR brain mitochondria exhibit functional plasticity following in vivo hypoxia; however, if and how these organelles tolerate ischaemia and how ischaemic stress impacts mitochondrial energetics and redox regulation is entirely unknown. We hypothesized that mitochondria fundamentally contribute to in vitro ischaemia resistance in the NMR brain. To test this, we treated NMR and CD-1 mouse cortical brain sheets with an in vitro ischaemic mimic and evaluated mitochondrial respiration capacity and redox regulation following 15 or 30 min of ischaemia or ischaemia/reperfusion (I/R). We found that, relative to mice, the NMR brain largely retains mitochondrial function and redox balance post-ischaemia and I/R. Specifically: (i) ischaemia reduced complex I and II-linked respiration ∼50-70% in mice, vs. ∼20-40% in NMR brain, (ii) NMR but not mouse brain maintained relatively steady respiration control ratios and robust mitochondrial membrane integrity, (iii) electron leakage post-ischaemia was lesser in NMR than mouse brain and NMR brain retained higher coupling efficiency, and (iv) free radical generation during and following ischaemia and I/R was lower from NMR brains than mice. Taken together, our results indicate that NMR brain mitochondria are more tolerant of ischaemia and I/R than mice and retain respiratory capacity while avoiding redox derangements. Overall, these findings support the hypothesis that hypoxia-tolerant NMR brain is also ischaemia-tolerant and suggest that NMRs may be a natural model of ischaemia tolerance in which to investigate evolutionarily derived solutions to ischaemic pathology. KEY POINTS: Ischaemia is highly deleterious to the mammalian brain and this damage is largely mediated by mitochondrial dysfunction. Naked mole-rats are among the most hypoxia-tolerant mammals and their brain tolerates ischaemia ex vivo, but the impact of ischaemia on mitochondrial function is unknown. Naked mole-rat but not mouse brain mitochondria retain respiratory capacity and membrane integrity following ischaemia or ischaemia/reperfusion. Differences in free radical management and respiratory pathway control between species may mediate this tolerance. These results help us understand how natural models of hypoxia tolerance also tolerate ischaemia in the brain." @default.
- W3198210902 created "2021-09-13" @default.
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- W3198210902 date "2021-09-28" @default.
- W3198210902 modified "2023-10-01" @default.
- W3198210902 title "Naked mole‐rat brain mitochondria tolerate <i>in vitro</i> ischaemia" @default.
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- W3198210902 cites W1964483580 @default.
- W3198210902 cites W1965285497 @default.
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- W3198210902 cites W1971050989 @default.
- W3198210902 cites W1973175579 @default.
- W3198210902 cites W1975202788 @default.
- W3198210902 cites W1975987540 @default.
- W3198210902 cites W1988534875 @default.
- W3198210902 cites W1989314662 @default.
- W3198210902 cites W1990242715 @default.
- W3198210902 cites W1992347206 @default.
- W3198210902 cites W2017546932 @default.
- W3198210902 cites W2029304051 @default.
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- W3198210902 cites W2037880817 @default.
- W3198210902 cites W2039276913 @default.
- W3198210902 cites W2045698094 @default.
- W3198210902 cites W2054120161 @default.
- W3198210902 cites W2064598952 @default.
- W3198210902 cites W2074661552 @default.
- W3198210902 cites W2076706063 @default.
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- W3198210902 doi "https://doi.org/10.1113/jp281942" @default.
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