Therapeutic Effect of Padina arborescens Extract on a Cell System Model for Parkinson’s Disease

Leucine-rich repeat kinase 2 (LRRK2) and α-synuclein are involved in the pathogenesis of Parkinson's disease. The activity of LRRK2 in microglial cells is associated with neuroinflammation, and LRRK2 inhibitors are crucial for alleviating this neuroinflammatory response. α-synuclein contributes to oxidative stress in the dopaminergic neuron and neuroinflammation through Toll-like receptors in microglia. In this study, we investigated the effect of the marine alga <i>Padina arborescens</i> on neuroinflammation by examining LRRK2 activation and the aggregation of α-synuclein. <i>P. arborescens</i> extract inhibits LRRK2 activity in vitro and decreases lipopolysaccharide (LPS)-induced LRRK2 upregulation in BV2, a mouse microglial cell line. Treatment with <i>P. arborescens</i> extract decreased tumor necrosis factor-α (TNF-α) gene expression by LPS through LRRK2 inhibition in BV2. It also attenuated TNF-α gene expression, inducible nitric oxide synthase, and the release of TNF-α and cellular nitric oxide in rat primary microglia. Furthermore, <i>P. arborescens</i> extract prevented rotenone (RTN)-induced oxidative stress in primary rat astrocytes and inhibited α-synuclein fibrilization in an in vitro assay using recombinant α-synuclein and in the differentiated human dopaminergic neuronal cell line SH-SY5Y (dSH). The extract increased lysosomal activity in dSH cells. In addition, <i>P. arborescens</i> extract slightly prolonged the lifespan of <i>Caenorhabditis elegans</i>, which was reduced by RTN treatment.

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Journal
NeuroSci
Published
2024-08-30
DOI
https://doi.org/10.3390/neurosci5030024
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
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0.00

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article

Therapeutic Effect of Padina arborescens Extract on a Cell System Model for Parkinson’s Disease

Dong Hwan Ho, Daleum Nam, Ilhong Son, Sung Woo Park et al.
NeuroSci
Neuroinflammation and Neurodegeneration Mechanisms
article

Therapeutic Effect of Padina arborescens Extract on a Cell System Model for Parkinson’s Disease

Dong Hwan Ho, Daleum Nam, Ilhong Son, Sung Woo Park, Dong‐Kyu Kim, Hye‐Jung Kim, Mi Kyoung Seo
article en

Abstract

Leucine-rich repeat kinase 2 (LRRK2) and α-synuclein are involved in the pathogenesis of Parkinson's disease. The activity of LRRK2 in microglial cells is associated with neuroinflammation, and LRRK2 inhibitors are crucial for alleviating this neuroinflammatory response. α-synuclein contributes to oxidative stress in the dopaminergic neuron and neuroinflammation through Toll-like receptors in microglia. In this study, we investigated the effect of the marine alga <i>Padina arborescens</i> on neuroinflammation by examining LRRK2 activation and the aggregation of α-synuclein. <i>P. arborescens</i> extract inhibits LRRK2 activity in vitro and decreases lipopolysaccharide (LPS)-induced LRRK2 upregulation in BV2, a mouse microglial cell line. Treatment with <i>P. arborescens</i> extract decreased tumor necrosis factor-α (TNF-α) gene expression by LPS through LRRK2 inhibition in BV2. It also attenuated TNF-α gene expression, inducible nitric oxide synthase, and the release of TNF-α and cellular nitric oxide in rat primary microglia. Furthermore, <i>P. arborescens</i> extract prevented rotenone (RTN)-induced oxidative stress in primary rat astrocytes and inhibited α-synuclein fibrilization in an in vitro assay using recombinant α-synuclein and in the differentiated human dopaminergic neuronal cell line SH-SY5Y (dSH). The extract increased lysosomal activity in dSH cells. In addition, <i>P. arborescens</i> extract slightly prolonged the lifespan of <i>Caenorhabditis elegans</i>, which was reduced by RTN treatment.

NeuroSciVol. 5(3)
Inje University (KR), The Catholic University of Korea Yeouido St. Mary's Hospital (KR), Inje University Busan Paik Hospital (KR), Wonkwang University (KR), Catholic University of Korea (KR)
Wonkwang University, National Marine Biodiversity Institute of Korea
Life below water
Openalex Percentile: Top 84%
Neuroinflammation and Neurodegeneration Mechanisms
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