Naproxen-Derived New Compound Inhibits the NF-κB, MAPK and PI3K/Akt Signaling Pathways Synergistically with Resveratrol in RAW264.7 Cells.
Yi OuZonglin YouMin YaoYingfan CaoXiu XueMin ChenRihui WuLishe GanDong-Li LiPanpan WuXuetao XuWing-Leung WongVincent Kam Wai WongWenfeng LiuJiming YeJing Wei JinPublished in: Molecules (Basel, Switzerland) (2023)
Naproxen is widely used for anti-inflammatory treatment but it can lead to serious side effects. To improve the anti-inflammatory activity and safety, a novel naproxen derivative containing cinnamic acid (NDC) was synthesized and used in combination with resveratrol. The results showed that the combination of NDC and resveratrol at different ratios have a synergistic anti-inflammatory efficacy in RAW264.7 macrophage cells. It was indicated that the combination of NDC and resveratrol at a ratio of 2:1 significantly inhibited the expression of carbon monoxide (NO), tumor necrosis factor α (TNF-α), interleukin 6 (IL-6), induced nitric oxide synthase (iNOS), cyclooxygenase 2 (COX-2) and reactive oxygen species (ROS) without detectable side effects on cell viability. Further studies revealed that these anti-inflammatory effects were mediated by the activation of nuclear factor kappa-B (NF-κB), mitogen-activated protein kinase (MAPK) and phosphoinositide-3 kinase (PI3K)/protein kinase B (Akt) signaling pathways, respectively. Taken together, these results highlighted the synergistic NDC and resveratrol anti-inflammatory activity that could be further explored as a strategy for the treatment of inflammatory disease with an improved safety profile.
Keyphrases
- signaling pathway
- pi k akt
- induced apoptosis
- cell cycle arrest
- nuclear factor
- nitric oxide synthase
- protein kinase
- cell proliferation
- anti inflammatory
- reactive oxygen species
- epithelial mesenchymal transition
- toll like receptor
- nitric oxide
- rheumatoid arthritis
- oxidative stress
- cell death
- poor prognosis
- cancer therapy
- endoplasmic reticulum stress
- high glucose
- inflammatory response
- tyrosine kinase
- diabetic rats
- long non coding rna
- binding protein
- dna damage