کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2068751 | 1078348 | 2013 | 10 صفحه PDF | دانلود رایگان |

Oxidative stress plays a role in a range of human disease entities. Hence, strategies to target antioxidants to mitochondria are an active area of investigation. Triphenylphosphonium cation-based antioxidants and SS-peptides have been described and show significant uptake by mitochondria and effectiveness in animal models of conditions linked to oxidative stress. We tested the hypothesis that the mitochondrial β-oxidation pathway could be exploited to activate the antioxidant phenolic and methimazole prodrugs. Most compounds studied underwent mitochondrial biotransformation to release their antioxidant moieties, and some were cytoprotective in a hypoxia–reoxygenation model in rat cardiomyocytes. These results demonstrate the feasibility of exploiting mitochondrial bioactivation reactions for targeted drug delivery.
► The mitochondrial targeting strategies currently being investigated are reviewed.
► The use of endobiotic metabolic pathways to target antioxidants to mitochondria is described.
► Preclinical and human clinical studies of mitochondria-targeted antioxidants are discussed.
Journal: Mitochondrion - Volume 13, Issue 5, September 2013, Pages 454–463