Ginsenoside Rg1 protects against H2O2‑induced neuronal damage due to inhibition of the NLRP1 inflammasome signalling pathway in hippocampal neurons in�vitro

Autor: Xiao‑Yan Shen, Tan‑Zhen Xu, Ling‑Ling Sun, Bi‑Qiong Zhang, Weizu Li, Da‑Ke Huang, Yali Chen
Rok vydání: 2018
Předmět:
0301 basic medicine
Senescence
Ginsenosides
Inflammasomes
hippocampal neurons
Interleukin-1beta
Apoptosis
NLR Proteins
Nerve Tissue Proteins
Hippocampal formation
medicine.disease_cause
Hippocampus
03 medical and health sciences
0302 clinical medicine
Genetics
medicine
Animals
Cells
Cultured

Neuroinflammation
Neurons
chemistry.chemical_classification
Reactive oxygen species
NADPH oxidase
reactive oxygen species oxidative stress
biology
NADPH oxidase 2
Caspase 1
Interleukin-18
Inflammasome
Articles
Hydrogen Peroxide
General Medicine
beta-Galactosidase
nucleotide-binding oligomerisation domain-like receptor protein 1 inflammasome
Rats
Cell biology
ginsenoside Rg1
Oxidative Stress
030104 developmental biology
chemistry
biology.protein
Reactive Oxygen Species
030217 neurology & neurosurgery
Oxidative stress
Central Nervous System Agents
Drugs
Chinese Herbal

Signal Transduction
medicine.drug
Zdroj: International Journal of Molecular Medicine
ISSN: 1791-244X
1107-3756
Popis: Oxidative stress and neuroinflammation are important in the pathogenesis of ageing and age‑related neurodegenerative diseases, including Alzheimer's disease. NADPH oxidase 2 (NOX2) is a major source of reactive oxygen species (ROS) in the brain. The nucleotide‑binding oligomerisation domain (NOD)‑like receptor protein 1 (NLRP1) inflammasome is responsible for the formation of pro‑inflammatory molecules in neurons. Whether the NOX2‑NLRP1 inflammasome signalling pathway is involved in neuronal ageing and age‑related damage remains to be elucidated. Ginsenoside Rg1 (Rg1) is a steroidal saponin found in ginseng. In the present study, the primary hippocampal neurons were treated with H2O2 (200 µM) and Rg1 (1, 5 and 10 µM) for 24 h to investigate the protective effects and mechanisms of Rg1 on H2O2‑induced hippocampal neuron damage, which mimics age‑related damage. The results showed that H2O2 treatment significantly increased ROS production and upregulated the expression of NOX2 and the NLRP1 inflammasome, and led to neuronal senescence and damage to hippocampal neurons. Rg1 decreased ROS production, reducing the expression of NOX2 and the NLRP1 inflammasome in H2O2‑treated hippocampal neurons. Furthermore, Rg1 and tempol treatment significantly decreased neuronal apoptosis and the expression of β‑galactosidase, and alleviated the neuronal senescence and damage induced by H2O2. The present study indicates that Rg1 may reduce NOX2‑mediated ROS generation, inhibit NLRP1 inflammasome activation, and inhibit neuronal senescence and damage.
Databáze: OpenAIRE