Ethanol Extract of Maclura tricuspidata Fruit Protects SH-SY5Y Neuroblastoma Cells against H2O2-Induced Oxidative Damage via Inhibiting MAPK and NF-κB Signaling.
Weishun TianSuyoung HeoDae-Woon KimIn-Shik KimDongchoon AhnHyun-Jin TaeMyung-Kon KimByung-Yong ParkPublished in: International journal of molecular sciences (2021)
Free radical generation and oxidative stress push forward an immense influence on the pathogenesis of neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. Maclura tricuspidata fruit (MT) contains many biologically active substances, including compounds with antioxidant properties. The current study aimed to investigate the neuroprotective effects of MT fruit on hydrogen peroxide (H2O2)-induced neurotoxicity in SH-SY5Y cells. SH-SY5Y cells were pretreated with MT, and cell damage was induced by H2O2. First, the chemical composition and free radical scavenging properties of MT were analyzed. MT attenuated oxidative stress-induced damage in cells based on the assessment of cell viability. The H2O2-induced toxicity caused by ROS production and lactate dehydrogenase (LDH) release was ameliorated by MT pretreatment. MT also promoted an increase in the expression of genes encoding the antioxidant enzymes superoxide dismutase (SOD) and catalase (CAT). MT pretreatment was associated with an increase in the expression of neuronal genes downregulated by H2O2. Mechanistically, MT dramatically suppressed H2O2-induced Bcl-2 downregulation, Bax upregulation, apoptotic factor caspase-3 activation, Mitogen-activated protein kinase (MAPK) (JNK, ERK, and p38), and Nuclear factor-κB (NF-κB) activation, thereby preventing H2O2-induced neurotoxicity. These results indicate that MT has protective effects against H2O2-induced oxidative damage in SH-SY5Y cells and can be used to prevent and protect against neurodegeneration.
Keyphrases
- induced apoptosis
- oxidative stress
- diabetic rats
- signaling pathway
- high glucose
- hydrogen peroxide
- cell cycle arrest
- endoplasmic reticulum stress
- cell death
- nuclear factor
- dna damage
- poor prognosis
- cell proliferation
- stem cells
- ischemia reperfusion injury
- nitric oxide
- gene expression
- immune response
- dna methylation
- single cell
- brain injury
- genome wide
- inflammatory response
- anti inflammatory
- transcription factor
- tyrosine kinase
- blood brain barrier
- binding protein