What is it about?
Increased expression of α-synuclein protein is central to the evolvement of neuropathology in Parkinson's disease (PD). The potential of ribose-cysteine and levodopa in abating α-synuclein-mediated PD was demonstrated in transgenic Drosophila model.
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Why is it important?
Long-term dopamine replacement therapy insensitivity is a drawback on levodopa. Therefore, there is a need for a product that can be used to manage the disease over a long period of time without side effects. Hence, ribose-cysteine, a glutathione booster, was explored in this study. Our findings show that ribose-cysteine and levodopa, both singly and in combination, potentiated a therapeutic effect on alpha-synuclein transgenic Drosophila melanogaster model of Parkinsonism.
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This page is a summary of: Ribose-cysteine and levodopa abrogate Parkinsonism via the regulation of neurochemical and redox activities in alpha-synuclein transgenic
Drosophila melanogaster
models, Fly, January 2024, Taylor & Francis,
DOI: 10.1080/19336934.2024.2306687.
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