Anti-Inflammatory Effects of Licania macrocarpa Cuatrec Methanol Extract Target Src- and TAK1-Mediated Pathways.
Kon Kuk ShinJae Gwang ParkYo Han HongNur AzizSang Hee ParkSunggyu KimEunji KimYoung-Jin SonPublished in: Evidence-based complementary and alternative medicine : eCAM (2019)
In this study, we investigated the anti-inflammatory effects of Licania macrocarpa Cuatrec methanol extract (Lm-ME) in vitro and in vivo and found pharmacological target proteins of Lm-ME in TLR4-mediated inflammatory signaling. This extract reduced NO production and mRNA expression of inflammatory cytokines such as iNOS, COX-2, IL-6, and IL-1β. In the NF-κB- and AP-1-mediated luciferase reporter gene assay, transcription factor activities decreased under cotransfection with MyD88 or TRIF. Phosphorylated protein levels of Src, PI3K, IKKα/β, and IκBα as well as p50 and p65 in the NF-κB signal pathway were downregulated, and phosphorylation of TAK1, MEK1/2, MKK4/7, and MKK3/6 as well as ERK, JNK, and p38 was decreased in the AP-1 signal pathway. Through overexpression of HA-Src and HA-TAK1, respectively, Lm-ME inhibited autophosphorylation of overexpressed proteins and thereby activated fewer downstream signaling molecules. Lm-ME also attenuated stomach ulcers in an HCl/EtOH-induced acute gastritis model mice, and COX-2 mRNA expression and phosphorylated TAK1 levels in gastric tissues were diminished. The flavonoids kaempferol and quercetin were identified in the HPLC analysis of Lm-ME; both are actively anti-inflammatory. Therefore, these results suggest that Lm-ME can be used for anti-inflammatory remedy by targeting Src and TAK1.
Keyphrases
- anti inflammatory
- transcription factor
- signaling pathway
- tyrosine kinase
- oxidative stress
- pi k akt
- toll like receptor
- cell proliferation
- inflammatory response
- lps induced
- helicobacter pylori
- gene expression
- nuclear factor
- crispr cas
- genome wide identification
- metabolic syndrome
- immune response
- mass spectrometry
- type diabetes
- small molecule
- simultaneous determination
- copy number
- high performance liquid chromatography
- high fat diet induced
- protein kinase
- dna methylation
- skeletal muscle
- wound healing
- binding protein
- insulin resistance
- tandem mass spectrometry