Inhibitory Effects of a Sargassum miyabei Yendo on Cutibacterium acnes-Induced Skin Inflammation.
Mi-Jin YimJeong Min LeeHyun-Soo KimGrace ChoiYoung-Mog KimDae-Sung LeeIl-Whan ChoiPublished in: Nutrients (2020)
Acne vulgaris is a chronic inflammatory condition of skin sebaceous follicles. To explore its effects on acne vulgaris, we investigated the antibacterial and anti-inflammatory activities of Sargassum miyabei Yendo (a brown alga) ethanolic extract (SMYEE) on Cutibacterium acnes (C. acnes)-stimulated inflammatory responses, both in vivo and in vitro. To induce inflammation in vivo, C. acnes was intradermally injected into the dorsal skin of mice, to which SMYEE was applied. The antimicrobial activity of SMYEE was evaluated by the determination of minimum inhibitory concentrations (MICs). To explore in vitro anti-inflammatory effects, HaCaT cells were stimulated with C. acnes after treatment with SMYEE. The levels of IL-8 and the underlying molecular effects in C. acnes-stimulated HaCaT cells were assessed by enzyme-linked immunosorbent assay, Western blotting, and an electrophoretic mobility shift assay. Mouse skin lesions improved after treatment with SMYEE (50 μg/mouse). Neutrophil infiltration was significantly reduced in SMYEE-treated compared to SMYEE-untreated skin lesions. SMYEE reversed the C. acnes-induced increase in IL-8 levels in HaCaT cells and suppressed dHL-60 cell migration. SMYEE also inhibited C. acnes-induced phosphorylation of the extracellular signal-regulated kinase and inhibited activator protein-1 signaling. SMYEE may be a useful treatment for C. acnes-induced acne vulgaris.
Keyphrases
- induced apoptosis
- oxidative stress
- diabetic rats
- high glucose
- soft tissue
- cell cycle arrest
- wound healing
- anti inflammatory
- cell migration
- drug induced
- spinal cord injury
- adipose tissue
- signaling pathway
- mass spectrometry
- type diabetes
- endothelial cells
- single cell
- neuropathic pain
- endoplasmic reticulum stress
- south africa
- small molecule
- skeletal muscle
- hidradenitis suppurativa
- insulin resistance
- nuclear factor
- protein protein
- newly diagnosed
- liquid chromatography