4.6 Article

Neurorescue Effects of Frondoside A and Ginsenoside Rg3 in C. elegans Model of Parkinson's Disease

Journal

MOLECULES
Volume 26, Issue 16, Pages -

Publisher

MDPI
DOI: 10.3390/molecules26164843

Keywords

Parkinson's disease; dopaminergic neurons; neurodegeneration; alpha-Synuclein; frondoside A; ginsenoside Rg3; Caenorhabditis elegans

Funding

  1. Mahidol University [2021-BRF2-NDFR27/2564]
  2. CIF grant, Faculty of Science, Mahidol University
  3. NIH Office of Research Infrastructure Programs [P40 OD010440]

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The study demonstrates that saponins from sea cucumber and ginseng have beneficial effects in rescuing dopaminergic neurodegeneration in C. elegans by suppressing apoptosis mediators and stimulating antioxidant enzymes. Additionally, frondoside A from sea cucumber can attenuate alpha-synuclein aggregation through the protein degradation process.
Parkinson's disease (PD) is a currently incurable neurodegenerative disorder characterized by the loss of dopaminergic (DAergic) neurons in the substantia nigra pars compacta and alpha-synuclein aggregation. Accumulated evidence indicates that the saponins, especially from ginseng, have neuroprotective effects against neurodegenerative disorders. Interestingly, saponin can also be found in marine organisms such as the sea cucumber, but little is known about its effect in neurodegenerative disease, including PD. In this study, we investigated the anti-Parkinson effects of frondoside A (FA) from Cucumaria frondosa and ginsenoside Rg3 (Rg3) from Panax notoginseng in C. elegans PD model. Both saponins were tested for toxicity and optimal concentration by food clearance assay and used to treat 6-OHDA-induced BZ555 and transgenic alpha-synuclein NL5901 strains in C. elegans. Treatment with FA and Rg3 significantly attenuated DAergic neurodegeneration induced by 6-OHDA in BZ555 strain, improved basal slowing rate, and prolonged lifespan in the 6-OHDA-induced wild-type strain with downregulation of the apoptosis mediators, egl-1 and ced-3, and upregulation of sod-3 and cat-2. Interestingly, only FA reduced alpha-synuclein aggregation, rescued lifespan in NL5901, and upregulated the protein degradation regulators, including ubh-4, hsf-1, hsp-16.1 and hsp-16.2. This study indicates that both FA and Rg3 possess beneficial effects in rescuing DAergic neurodegeneration in the 6-OHDA-induced C. elegans model through suppressing apoptosis mediators and stimulating antioxidant enzymes. In addition, FA could attenuate alpha-synuclein aggregation through the protein degradation process.

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