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Mitochondrial transplantation strategies as potential therapeutics for central nervous system trauma

Producción científica: Review articlerevisión exhaustiva

56 Citas (Scopus)

Resumen

Mitochondria are essential cellular organelles critical for generating adenosine triphosphate for cellular homeostasis, as well as various mechanisms that can lead to both necrosis and apoptosis. The field of "mitochondrial medicine" is emerging in which injury/disease states are targeted therapeutically at the level of the mitochondrion, including specific antioxidants, bioenergetic substrate additions, and membrane uncoupling agents. Consequently, novel mitochondrial transplantation strategies represent a potentially multifactorial therapy leading to increased adenosine triphosphate production, decreased oxidative stress, mitochondrial DNA replacement, improved bioenergetics and tissue sparing. Herein, we describe briefly the history of mitochondrial transplantation and the various techniques used for both in vitro and in vivo delivery, the benefits associated with successful transference into both peripheral and central nervous system tissues, along with caveats and pitfalls that hinder the advancements of this novel therapeutic.

Idioma originalEnglish
Páginas (desde-hasta)194-197
Número de páginas4
PublicaciónNeural Regeneration Research
Volumen13
N.º2
DOI
EstadoPublished - feb 2018

Nota bibliográfica

Publisher Copyright:
© 2018 Wolters Kluwer Medknow Publications. All rights reserved.

Financiación

Author contributions: JLG, SPP and AGR wrote the paper. Conflicts of interest: None declared. Financial support: This work was funded by NIH R21NS096670 (AGR), University of Kentucky Spinal Cord and Brain Injury Research Center Chair Endowment (AGR), NIH/NINDS 2P30NS051220. Plagiarism check: Checked twice by iThenticate. Peer review: Externally peer reviewed. Open access statement: This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-Shar-eAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under identical terms. Funding: This work was funded by NIH R21NS096670 (AGR), University of Kentucky Spinal Cord and Brain Injury Research Center Chair Endowment (AGR), NIH/NINDS 2P30NS051220.

FinanciadoresNúmero del financiador
NIH/NINDS2P30NS051220
National Institutes of Health (NIH)R21NS096670
University of Kentucky

    ASJC Scopus subject areas

    • Developmental Neuroscience

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