دورية أكاديمية
Clinically relevant mitochondrial-targeted therapy improves chronic outcomes after traumatic brain injury
| العنوان: | Clinically relevant mitochondrial-targeted therapy improves chronic outcomes after traumatic brain injury |
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| المؤلفون: | Hubbard, W Brad, Spry, Malinda L, Gooch, Jennifer L, Cloud, Amber L, Vekaria, Hemendra J, Burden, Shawn, Powell, David K, Berkowitz, Bruce A, Geldenhuys, Werner J, Harris, Neil G, Sullivan, Patrick G |
| المساهمون: | BLR&D Department of Veterans Affairs Merit, Kentucky Spinal Cord and Head Injury Research Trust, NIH, BLR&D Career Development Award, Department of Veterans Affairs, National Institutes of Health, U.S. Department of Veterans Affairs, United States Government |
| المصدر: | Brain ; volume 144, issue 12, page 3788-3807 ; ISSN 0006-8950 1460-2156 |
| بيانات النشر: | Oxford University Press (OUP) |
| سنة النشر: | 2021 |
| الوصف: | Pioglitazone, an FDA-approved compound, has been shown to target the novel mitochondrial protein mitoNEET and produce short-term neuroprotection and functional benefits following traumatic brain injury. To expand on these findings, we now investigate the dose- and time-dependent effects of pioglitazone administration on mitochondrial function after experimental traumatic brain injury. We then hypothesize that optimal pioglitazone dosing will lead to ongoing neuroprotection and cognitive benefits that are dependent on pioglitazone-mitoNEET signalling pathways. We show that delayed intervention is significantly more effective than early intervention at improving acute mitochondrial bioenergetics in the brain after traumatic brain injury. In corroboration, we demonstrate that mitoNEET is more heavily expressed, especially near the cortical contusion, in the 18 h following traumatic brain injury. To explore whether these findings relate to ongoing pathological and behavioural outcomes, mice received controlled cortical impact followed by initiation of pioglitazone treatment at either 3 or 18 h post-injury. Mice with treatment initiation at 18 h post-injury exhibited significantly improved behaviour and tissue sparing compared to mice with pioglitazone initiated at 3 h post-injury. Further using mitoNEET knockout mice, we show that this therapeutic effect is dependent on mitoNEET. Finally, we demonstrate that delayed pioglitazone treatment improves serial motor and cognitive performance in conjunction with attenuated brain atrophy after traumatic brain injury. This study illustrates that mitoNEET is the critical target for delayed pioglitazone intervention after traumatic brain injury, mitochondrial-targeting is highly time-dependent after injury and there is an extended therapeutic window to effectively treat mitochondrial dysfunction after brain injury. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| DOI: | 10.1093/brain/awab341 |
| الإتاحة: | https://doi.org/10.1093/brain/awab341Test https://academic.oup.com/brain/article-pdf/144/12/3788/42004653/awab341.pdfTest |
| حقوق: | https://creativecommons.org/licenses/by-nc/4.0Test/ |
| رقم الانضمام: | edsbas.66FABCE3 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1093/brain/awab341 |
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