Rapamycin administration is not a valid therapeutic strategy for every case of mitochondrial disease
Author(s) -
Eliana BarriocanalCasado,
Agustín HidalgoGutiérrez,
Nuno Raimundo,
Pilar González-García,
Darío AcuñaCastroviejo,
Germaine Escames,
Luís C. López
Publication year - 2019
Publication title -
ebiomedicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.596
H-Index - 63
ISSN - 2352-3964
DOI - 10.1016/j.ebiom.2019.03.025
Subject(s) - administration (probate law) , disease , medicine , mitochondrial disease , medline , bioinformatics , pharmacology , mitochondrial dna , intensive care medicine , biology , pathology , genetics , political science , gene , biochemistry , law
The vast majority of mitochondrial disorders have limited the clinical management to palliative care. Rapamycin has emerged as a potential therapeutic drug for mitochondrial diseases since it has shown therapeutic benefits in a few mouse models of mitochondrial disorders. However, the underlying therapeutic mechanism is unclear, the minimal effective dose needs to be defined and whether this therapy can be generally used is unknown.
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