Extract from Black Soybean Cultivar A63 Extract Ameliorates Atopic Dermatitis-like Skin Inflammation in an Oxazolone-Induced Murine Model.
Banzragch DorjsembeChu Won NhoYongsoo ChoiJin-Chul KimPublished in: Molecules (Basel, Switzerland) (2022)
Black soybean has been used in traditional medicine to treat inflammatory diseases, cancer, and diabetes and as a nutritional source since ancient times. We found that Korean black soybean cultivar A63 has more cyanidin-3- O -glucoside, (C3G), procyanidin B2 (PB2), and epicatechin (EPC) contents than other cultivars and has beneficial effects on cell viability and anti-oxidation. Given the higher concentration of anthocyanidins and their strong anti-oxidant activity, we predicted that A63 extract could relieve inflammatory disease symptoms, including those of atopic dermatitis (AD). Here, we evaluated the anti-AD activity of A63 extract in an oxazolone (OXA)-induced mouse model. A63 extract treatment significantly reduced epidermal thickness and inflammatory cell infiltration, downregulated the expression of AD gene markers, including Interleukin (IL)-4 and IL-5, and restored damaged skin barrier tissues. Furthermore, A63 extract influenced the activation of the signal transducer and activator of transcription (STAT) 3 and STAT6, extracellular regulatory kinase (ERK), and c-Jun N-terminal kinase (JNK) signaling pathways, which play a crucial role in the development of AD. Altogether, our results suggest that A63 can ameliorate AD-like skin inflammation by inhibiting inflammatory cytokine production and STAT3/6 and Mitogen-activated protein kinase (MAPK) signaling and restoring skin barrier function.
Keyphrases
- oxidative stress
- diabetic rats
- signaling pathway
- induced apoptosis
- atopic dermatitis
- mouse model
- anti inflammatory
- wound healing
- cell proliferation
- soft tissue
- poor prognosis
- pi k akt
- type diabetes
- gene expression
- high glucose
- protein kinase
- single cell
- stem cells
- transcription factor
- physical activity
- tyrosine kinase
- cell therapy
- metabolic syndrome
- drug induced
- risk assessment
- klebsiella pneumoniae
- epithelial mesenchymal transition
- papillary thyroid
- cell death
- multidrug resistant
- toll like receptor
- nuclear factor
- mesenchymal stem cells
- hydrogen peroxide
- endoplasmic reticulum stress
- stress induced
- insulin resistance
- drug resistant
- combination therapy
- adipose tissue