Please use this identifier to cite or link to this item: http://buratest.brunel.ac.uk/handle/2438/12095
Title: Targeting lipid peroxidation and mitochondrial imbalance in Friedreich's ataxia
Authors: Abeti, R
Uzun, E
Renganathan, I
Honda, T
Pook, MA
Giunti, P
Keywords: Friedreich's ataxia;Lipid peroxidation;Mitochondria;Oxidative stress;Poly-unsaturated fatty acids;Nuclear factor E2 related factor
Issue Date: 2015
Publisher: Elsevier
Citation: Pharmacological Research, 99: pp. 344 - 350, (2015)
Abstract: Friedreich's ataxia (FRDA) is an autosomal recessive disorder, caused by reduced levels of the protein frataxin. This protein is located in the mitochondria, where it functions in the biogenesis of iron-sulphur clusters (ISCs), which are important for the function of the mitochondrial respiratory chain complexes. Moreover, disruption in iron biogenesis may lead to oxidative stress. Oxidative stress can be the cause and/or the consequence of mitochondrial energy imbalance, leading to cell death. Fibroblasts from two FRDA mouse models, YG8R and KIKO, were used to analyse two different categories of protective compounds: deuterised poly-unsaturated fatty acids (dPUFAs) and Nrf2-inducers. The former have been shown to protect the cell from damage induced by lipid peroxidation and the latter trigger the well-known Nrf2 antioxidant pathway. Our results show that the sensitivity to oxidative stress of YG8R and KIKO mouse fibroblasts, resulting in cell death and lipid peroxidation, can be prevented by d4-PUFA and Nrf2-inducers (SFN and TBE-31). The mitochondrial membrane potential (ΔΨ<inf>m</inf>) of YG8R and KIKO fibroblasts revealed a difference in their mitochondrial pathophysiology, which may be due to the different genetic basis of the two models. This suggests that variable levels of reduced frataxin may act differently on mitochondrial pathophysiology and that these two cell models could be useful in recapitulating the observed differences in the FRDA phenotype. This may reflect a different modulatory effect towards cell death that will need to be investigated further.
URI: http://www.sciencedirect.com/science/article/pii/S1043661815001139
http://bura.brunel.ac.uk/handle/2438/12095
DOI: http://dx.doi.org/10.1016/j.phrs.2015.05.015
ISSN: 1043-6618
1096-1186
Appears in Collections:Dept of Life Sciences Research Papers

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