δ-Tocotrienol, Isolated from Rice Bran, Exerts an Anti-Inflammatory Effect via MAPKs and PPARs Signaling Pathways in Lipopolysaccharide-Stimulated Macrophages.
Junjun ShenTao YangYouzhi XuYi LuoXinyue ZhongLimin ShiTao HuTianyi GuoYing NieFei Jun LuoQinlu LinPublished in: International journal of molecular sciences (2018)
δ-Tocotrienol, an important component of vitamin E, has been reported to possess some physiological functions, such as anticancer and anti-inflammation, however their molecular mechanisms are not clear. In this study, δ-tocotrienol was isolated and purified from rice bran. The anti-inflammatory effect and mechanism of δ-tocotrienol against lipopolysaccharides (LPS) activated pro-inflammatory mediator expressions in RAW264.7 cells were investigated. Results showed that δ-tocotrienol significantly inhibited LPS-stimulated nitric oxide (NO) and proinflammatory cytokine (TNF-α, IFN-γ, IL-1β and IL-6) production and blocked the phosphorylation of c-Jun N-terminal kinase (JNK) and extracellular regulated protein kinases 1/2 (ERK1/2). δ-Tocotrienol repressed the transcriptional activations and translocations of nuclear factor-kappa B (NF-κB) and activator protein-1 (AP-1), which were closely related with downregulated cytokine expressions. Meanwhile, δ-tocotrienol also affected the PPAR signal pathway and exerted an anti-inflammatory effect. Taken together, our data showed that δ-tocotrienol inhibited inflammation via mitogen-activated protein kinase (MAPK) and peroxisome proliferator-activated receptor (PPAR) signalings in LPS-stimulated macrophages.
Keyphrases
- anti inflammatory
- nuclear factor
- signaling pathway
- toll like receptor
- induced apoptosis
- inflammatory response
- oxidative stress
- pi k akt
- nitric oxide
- transcription factor
- insulin resistance
- cell cycle arrest
- metabolic syndrome
- immune response
- lps induced
- cell death
- epithelial mesenchymal transition
- adipose tissue
- endoplasmic reticulum stress
- dendritic cells
- machine learning
- binding protein
- fatty acid
- amino acid
- artificial intelligence
- nitric oxide synthase
- drug induced
- single molecule