TitleCu(atsm) improves the neurological phenotype and survival of SOD1 mice and selectively increases enzymatically active SOD1 in the spinal cord.
Publication TypeJournal Article
Year of Publication2017
AuthorsHilton JB, Mercer SW, Lim NKH, Faux NG, Buncic G, Beckman JS, Roberts BR, Donnelly PS, White AR, Crouch PJ
JournalSci Rep
Volume7
Pagination42292
Date Published2017 02 13
ISSN2045-2322
KeywordsAdministration, Oral, Animals, Copper, Cytochromes c, Gliosis, Humans, Liver, Mice, Transgenic, Mitochondria, Motor Neurons, Mutation, Organometallic Compounds, Oxidative Stress, Phenotype, Spinal Cord, Superoxide Dismutase, Survival Analysis, Thiosemicarbazones, Tissue Extracts
Abstract

Ubiquitous expression of mutant Cu/Zn-superoxide dismutase (SOD1) selectively affects motor neurons in the central nervous system (CNS), causing the adult-onset degenerative disease amyotrophic lateral sclerosis (ALS). The CNS-specific impact of ubiquitous mutant SOD1 expression is recapitulated in transgenic mouse models of the disease. Here we present outcomes for the metallo-complex Cu(atsm) tested for therapeutic efficacy in mice expressing SOD1 on a mixed genetic background. Oral administration of Cu(atsm) delayed the onset of neurological symptoms, improved locomotive capacity and extended overall survival. Although the ALS-like phenotype of SOD1 mice is instigated by expression of the mutant SOD1, we show the improved phenotype of the Cu(atsm)-treated animals involves an increase in mature mutant SOD1 protein in the disease-affected spinal cord, where concomitant increases in copper and SOD1 activity are also evident. In contrast to these effects in the spinal cord, treating with Cu(atsm) had no effect in liver on either mutant SOD1 protein levels or its activity, indicating a CNS-selective SOD1 response to the drug. These data provide support for Cu(atsm) as a treatment option for ALS as well as insight to the CNS-selective effects of mutant SOD1.

DOI10.1038/srep42292
Alternate JournalSci Rep
PubMed ID28205575
PubMed Central IDPMC5304223