Neuroprotective effects of PRG on Aβ 25-35 -induced cytotoxicity through activation of the ERK1/2 signaling pathway

Phylloporia ribis (Schumach:Fr.)Ryvarden is a genus of needle Phellinus medicinal fungi, parasitic on the living rhizomes of hawthorn and pear trees. As a traditional Chinese medicine, Phylloporia ribis was used in folklore for long-term illness, weakness and memory loss in old age. Previous studies...

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Veröffentlicht in:Journal of ethnopharmacology 2023-09, Vol.313, p.116550
Hauptverfasser: Bian, Zhiying, Cao, Chenzhen, Ding, Jie, Ding, Liang, Yu, Shuai, Zhang, Chuanxiang, Liu, Qian, Zhu, Lihao, Li, Jing, Zhang, Yongqing, Liu, Yuhong
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container_title Journal of ethnopharmacology
container_volume 313
creator Bian, Zhiying
Cao, Chenzhen
Ding, Jie
Ding, Liang
Yu, Shuai
Zhang, Chuanxiang
Liu, Qian
Zhu, Lihao
Li, Jing
Zhang, Yongqing
Liu, Yuhong
description Phylloporia ribis (Schumach:Fr.)Ryvarden is a genus of needle Phellinus medicinal fungi, parasitic on the living rhizomes of hawthorn and pear trees. As a traditional Chinese medicine, Phylloporia ribis was used in folklore for long-term illness, weakness and memory loss in old age. Previous studies have shown that polysaccharides from Phylloporia ribis (PRG) significantly promoted synaptic growth in PC12 cells in a dose-dependent manner, exhibiting "NGF"-like neurotrophic activity. Aβ damage to PC12 cells produced neurotoxicity and decreased cell survival, and PRG reduced the apoptosis rate, suggesting that PRG has neuroprotective effects. The studies confirmed that PRG had the potential to be a neuroprotective agent, but its neuroprotective mechanism remained unclear. We aimed to elucidate the neuroprotective effects of PRG in an Aβ -induced Alzheimer's disease (AD) model. Highly-differentiated PC12 cells were treated with Aβ (AD model) and PRG, and were assessed for cellular apoptosis, inflammatory factors, oxidative stress, and kinase phosphorylation. The results showed that the PRG groups effectively inhibited the neurotoxicity, mainly manifested by inhibiting mitochondrial oxidative stress, attenuating neuroinflammatory responses, and improving mitochondrial energy metabolism, eventually resulting in higher cell survival. The expression of p-ERK, p-CREB and BDNF proteins was increased in the PRG groups compared to the model group, which confirmed that PRG reversed the inhibition of the ERK pathway. We provide evidence for neuroprotection conferred by PRG and its mechanism by inhibiting ERK1/2 hyper-phosphorylation, prevention of mitochondrial stress, and subsequent prevention of apoptosis. The study highlights PRG as a promising candidate with neuroprotective effects, the potential of which can be harnessed for identifying novel therapeutic targets.
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As a traditional Chinese medicine, Phylloporia ribis was used in folklore for long-term illness, weakness and memory loss in old age. Previous studies have shown that polysaccharides from Phylloporia ribis (PRG) significantly promoted synaptic growth in PC12 cells in a dose-dependent manner, exhibiting "NGF"-like neurotrophic activity. Aβ damage to PC12 cells produced neurotoxicity and decreased cell survival, and PRG reduced the apoptosis rate, suggesting that PRG has neuroprotective effects. The studies confirmed that PRG had the potential to be a neuroprotective agent, but its neuroprotective mechanism remained unclear. We aimed to elucidate the neuroprotective effects of PRG in an Aβ -induced Alzheimer's disease (AD) model. Highly-differentiated PC12 cells were treated with Aβ (AD model) and PRG, and were assessed for cellular apoptosis, inflammatory factors, oxidative stress, and kinase phosphorylation. The results showed that the PRG groups effectively inhibited the neurotoxicity, mainly manifested by inhibiting mitochondrial oxidative stress, attenuating neuroinflammatory responses, and improving mitochondrial energy metabolism, eventually resulting in higher cell survival. The expression of p-ERK, p-CREB and BDNF proteins was increased in the PRG groups compared to the model group, which confirmed that PRG reversed the inhibition of the ERK pathway. We provide evidence for neuroprotection conferred by PRG and its mechanism by inhibiting ERK1/2 hyper-phosphorylation, prevention of mitochondrial stress, and subsequent prevention of apoptosis. 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subjects Alzheimer Disease - drug therapy
Amyloid beta-Peptides - metabolism
Amyloid beta-Peptides - toxicity
Animals
Apoptosis
Cell Survival
Humans
MAP Kinase Signaling System
Neuroprotective Agents - pharmacology
Neuroprotective Agents - therapeutic use
Neurotoxicity Syndromes
PC12 Cells
Peptide Fragments - metabolism
Rats
Signal Transduction
title Neuroprotective effects of PRG on Aβ 25-35 -induced cytotoxicity through activation of the ERK1/2 signaling pathway
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