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Antioxidants can inhibit basal autophagy and enhance neurodegeneration in models of polyglutamine disease.

Published version
Peer-reviewed

Type

Article

Change log

Authors

Underwood, Benjamin R 
Imarisio, Sara 
Rose, Claudia 
Krishna, Gauri 

Abstract

Many neurodegenerative diseases exhibit protein accumulation and increased oxidative stress. Therapeutic strategies include clearing aggregate-prone proteins by enhancing autophagy or decreasing oxidative stress with antioxidants. Many autophagy-inducing stimuli increase reactive oxygen species (ROS), raising concerns that the benefits of autophagy up-regulation may be counterbalanced by ROS toxicity. Here we show that not all autophagy inducers significantly increase ROS. However, many antioxidants inhibit both basal and induced autophagy. By blocking autophagy, antioxidant drugs can increase the levels of aggregate-prone proteins associated with neurodegenerative disease. In fly and zebrafish models of Huntington's disease, antioxidants exacerbate the disease phenotype and abrogate the rescue seen with autophagy-inducing agents. Thus, the potential benefits in neurodegenerative diseases of some classes of antioxidants may be compromised by their autophagy-blocking properties.

Description

Keywords

Animals, Antioxidants, Autophagy, COS Cells, Chlorocebus aethiops, Disease Models, Animal, Drosophila, HeLa Cells, Humans, Mice, Mice, Inbred C57BL, Neurodegenerative Diseases, Oxidative Stress, Peptides, Reactive Oxygen Species, Zebrafish

Journal Title

Hum Mol Genet

Conference Name

Journal ISSN

0964-6906
1460-2083

Volume Title

19

Publisher

Oxford University Press (OUP)
Sponsorship
Medical Research Council (G0600194)
Medical Research Council (G0901339)
Medical Research Council (MC_U105663142)