Impaired striatal glutathione–ascorbate metabolism induces transient dopamine increase and motor dysfunction

Identifying initial triggering events in neurodegenerative disorders is critical to developing preventive therapies. In Huntington's disease (HD), hyperdopaminergia-probably triggered by the dysfunction of the most affected neurons, indirect pathway spiny projection neurons (iSPNs)-is believed to induce hyperkinesia, an early stage HD symptom. However, how this change arises and contributes to HD pathogenesis is unclear. Here, we demonstrate that genetic disruption of iSPNs function by Ntrk2/Trkb deletion in mice results in increased striatal dopamine and midbrain dopaminergic neurons, preceding hyperkinetic dysfunction. Transcriptomic analysis of iSPNs at the pre-symptomatic stage showed de-regulation of metabolic pathways, including upregulation of Gsto2, encoding glutathione S-transferase omega-2 (GSTO2). Selectively reducing Gsto2 in iSPNs in vivo effectively prevented dopaminergic dysfunction and halted the onset and progression of hyperkinetic symptoms. This study uncovers a functional link between altered iSPN BDNF-TrkB signalling, glutathione-ascorbate metabolism and hyperdopaminergic state, underscoring the vital role of GSTO2 in maintaining dopamine balance.

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Publication Details

Journal
Nature Metabolism
Published
2024-10-28
DOI
https://doi.org/10.1038/s42255-024-01155-z
Citations
5
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
1.34

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article

Impaired striatal glutathione–ascorbate metabolism induces transient dopamine increase and motor dysfunction

Kerstin N. Timm, Peter J. Magill, Nikolaos Barkas, Aleksandra Wolska et al.
5 citations
Nature Metabolism
Genetic Neurodegenerative Diseases
1.34
article

Impaired striatal glutathione–ascorbate metabolism induces transient dopamine increase and motor dysfunction

Kerstin N. Timm, Peter J. Magill, Nikolaos Barkas, Aleksandra Wolska, Liliana Minichiello, Mark E. Walton, Barbara Zonta, Claus Nerlov, Stephan von Hörsten, Veronika Ratz, E.A. Eliseeva, Vasileios Eftychidis, David A. Bergin, Aman Asif-Malik, Guo Fei, Mohd Yaseen Malik
article en
5 citations

Abstract

Identifying initial triggering events in neurodegenerative disorders is critical to developing preventive therapies. In Huntington's disease (HD), hyperdopaminergia-probably triggered by the dysfunction of the most affected neurons, indirect pathway spiny projection neurons (iSPNs)-is believed to induce hyperkinesia, an early stage HD symptom. However, how this change arises and contributes to HD pathogenesis is unclear. Here, we demonstrate that genetic disruption of iSPNs function by Ntrk2/Trkb deletion in mice results in increased striatal dopamine and midbrain dopaminergic neurons, preceding hyperkinetic dysfunction. Transcriptomic analysis of iSPNs at the pre-symptomatic stage showed de-regulation of metabolic pathways, including upregulation of Gsto2, encoding glutathione S-transferase omega-2 (GSTO2). Selectively reducing Gsto2 in iSPNs in vivo effectively prevented dopaminergic dysfunction and halted the onset and progression of hyperkinetic symptoms. This study uncovers a functional link between altered iSPN BDNF-TrkB signalling, glutathione-ascorbate metabolism and hyperdopaminergic state, underscoring the vital role of GSTO2 in maintaining dopamine balance.

Nature MetabolismVol. 6(11)
Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), John Radcliffe Hospital (GB), University of Oxford (GB), Wellcome Centre for Integrative Neuroimaging (GB), MRC Brain Network Dynamics Unit (GB), MRC Weatherall Institute of Molecular Medicine (GB)
Medical Research Council, Biotechnology and Biological Sciences Research Council
Good health and well-being
Openalex Percentile: Top 20%
Genetic Neurodegenerative Diseases
1.34
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