5-Hydroxymaltol Derived from Beetroot Juice through Lactobacillus Fermentation Suppresses Inflammatory Effect and Oxidant Stress via Regulating NF-kB, MAPKs Pathway and NRF2/HO-1 Expression.
Su-Lim KimHack Sun ChoiYu-Chan KoBong-Sik YunDong-Sun LeePublished in: Antioxidants (Basel, Switzerland) (2021)
Inflammation is the first response of the immune system against bacterial pathogens. This study isolated and examined an antioxidant derived from Lactobacillus fermentation products using cultured media with 1% beet powder. The antioxidant activity of the beet culture media was significantly high. Antioxidant activity-guided purification and repeated sample isolation yielded an isolated compound, which was identified as 5-hydoxymaltol using nuclear magnetic resonance spectrometry. We examined the mechanism of its protective effect on lipopolysaccharide (LPS)-induced inflammation of macrophages. 5-Hydroxymaltol suppressed nitric oxide (NO) production in LPS-stimulated RAW 264.7 cells. It also suppressed tumor necrosis factor α (TNF-α), interleukin (IL)-1β, and inducible nitric oxide synthase (iNOS) in the messenger RNA and protein levels in LPS-treated RAW 264.7 cells. Moreover, it suppressed LPS-induced nuclear translocation of NF-κB (p65) and mitogen-activated protein kinase activation. Furthermore, 5-hydroxymaltol reduced LPS-induced reactive oxygen species (ROS) production as well as increased nuclear factor erythroid 2-related factor 2 and heme oxygenase 1 expression. Overall, this study found that 5-hydroxymaltol has anti-inflammatory activities in LPS-stimulated RAW 264.7 macrophage cells based on its inhibition of pro-inflammatory cytokine production depending on the nuclear factor κB signaling pathway, inhibition of LPS-induced reactive oxygen species production, inhibition of LPS-induced mitogen-activated protein kinase induction, and induction of the nuclear factor erythroid 2-related factor 2/heme oxygenase 1 signaling pathway. Our data showed that 5-hydroxymaltol may be an effective compound for treating inflammation-mediated diseases.
Keyphrases
- lps induced
- inflammatory response
- nuclear factor
- toll like receptor
- induced apoptosis
- oxidative stress
- signaling pathway
- anti inflammatory
- reactive oxygen species
- nitric oxide
- nitric oxide synthase
- cell cycle arrest
- pi k akt
- magnetic resonance
- rheumatoid arthritis
- poor prognosis
- cell death
- endoplasmic reticulum stress
- lactic acid
- epithelial mesenchymal transition
- endothelial cells
- immune response
- computed tomography
- adipose tissue
- dna damage
- magnetic resonance imaging
- tyrosine kinase
- protein kinase
- long non coding rna
- cell proliferation
- machine learning
- amino acid
- saccharomyces cerevisiae
- artificial intelligence
- big data