Fermented Lettuce Extract Containing Nitric Oxide Metabolites Attenuates Inflammatory Parameters in Model Mice and in Human Fibroblast-Like Synoviocytes.
Jisu ParkJi Hyeon RyuBo-Young KimHyun Soo ChunMin Sun KimYong Il ShinPublished in: Nutrients (2023)
Lettuce ( Lactuca sativa L.) contains various bioactive compounds that can reduce the severity of inflammatory diseases. This study aimed to identify therapeutic effects and underlying mechanisms of fermented lettuce extract (FLE) containing stable nitric oxide (NO) on collagen-induced arthritis (CIA) in mice and fibroblast-like synoviocytes (MH7A line) from patients with rheumatoid arthritis (RA). DBA/1 mice were immunized with bovine type II collagen and orally administered FLE for 14 days. On day 36, mouse sera and ankle joints were collected for serological and histological analysis, respectively. Consuming FLE inhibited RA development, suppressing pro-inflammatory cytokine productions, synovial inflammation, and cartilage degradation. The therapeutic effects of FLE in CIA mice were similar to those of methotrexate (MTX), which is typically used to treat RA. In vitro, FLE suppressed the transforming growth factor-β (TGF-β)/Smad signaling pathway in MH7A cells. We also demonstrated that FLE inhibited TGF-β-induced cell migration, suppressed MMP-2/9 expression, inhibited MH7A cell proliferation, and increased the expression of autophagy markers LC3B and p62 in a dose-dependent manner. Our data suggest that FLE could induce autophagosome formations in the early of stages of autophagy while inhibiting their degradation in the later stages. In conclusion, FLE is a potential therapeutic agent for RA.
Keyphrases
- transforming growth factor
- signaling pathway
- oxidative stress
- nitric oxide
- epithelial mesenchymal transition
- rheumatoid arthritis
- cell migration
- induced apoptosis
- high fat diet induced
- diabetic rats
- cell proliferation
- poor prognosis
- pi k akt
- disease activity
- cell death
- ankylosing spondylitis
- high glucose
- wound healing
- cell cycle arrest
- interstitial lung disease
- nitric oxide synthase
- hydrogen peroxide
- wild type
- systemic lupus erythematosus
- drug induced
- ms ms
- systemic sclerosis
- skeletal muscle
- long non coding rna
- insulin resistance
- deep learning
- idiopathic pulmonary fibrosis
- anti inflammatory
- extracellular matrix
- artificial intelligence
- data analysis