Protective Effects of Ferulic Acid on Deoxynivalenol-Induced Toxicity in IPEC-J2 Cells.
Xiangyi MengWenyan YuNuo DuanZhouping WangYing-Bin ShenShijia WuPublished in: Toxins (2022)
Deoxynivalenol (DON), a mycotoxin that contaminates crops such as wheat and corn, can cause severe acute or chronic injury when ingested by animals or humans. This study investigated the protective effect of ferulic acid (FA), a polyphenolic substance, on alleviating the toxicity induced by DON (40 μM) in IPEC-J2 cells. The experiments results showed that FA not only alleviated the decrease in cell viability caused by DON ( p < 0.05), but increased the level of superoxide dismutase (SOD) ( p < 0.01), glutathione peroxidase (GSH-Px), (catalase) CAT and glutathione (GSH) ( p < 0.05) through the nuclear factor erythroid 2-related factor 2 (Nrf2)-epoxy chloropropane Kelch sample related protein-1 (keap1) pathway, and then decreased the levels of intracellular oxidative stress. Additionally, FA could alleviate DON-induced inflammation through mitogen-activated protein kinases (MAPKs) and nuclear factor kappa-B (NF-κB) pathways, down-regulated the secretion of interleukin-6 (IL-6) ( p < 0.0001), interleukin-8 (IL-8) ( p < 0.05), interleukin-1β (IL-1β), interferon-γ (IFN-γ) and further attenuated the DON-induced intracellular apoptosis (10.7% to 6.84%) by regulating the expression of Bcl2-associated X protein (Bax) ( p < 0.0001), B-cell lymphoma-2 (Bcl-2) ( p < 0.0001), and caspase-3 ( p < 0.0001). All these results indicate that FA exhibits a significantly protective effect against DON-induced toxicity.
Keyphrases
- oxidative stress
- nuclear factor
- diabetic rats
- induced apoptosis
- toll like receptor
- high glucose
- cell cycle arrest
- endoplasmic reticulum stress
- drug induced
- dna damage
- signaling pathway
- cell death
- ischemia reperfusion injury
- immune response
- poor prognosis
- dendritic cells
- endothelial cells
- transcription factor
- nitric oxide
- pi k akt
- cell proliferation
- protein protein
- reactive oxygen species
- long non coding rna
- mass spectrometry
- amyotrophic lateral sclerosis