Micro-Current Stimulation Suppresses Inflammatory Responses in Peptidoglycan-Treated Raw 264.7 Macrophages and Propionibacterium acnes -Induced Skin Inflammation via TLR2/NF-κB Signaling Pathway.
Hana LeeDonghyun HwangMinjoo LeeJinho LeeSeungkwan ChoTack-Joong KimHan Sung KimPublished in: International journal of molecular sciences (2022)
Acne is a common inflammatory disorder of the human skin and a multifactorial disease caused by the sebaceous gland and Propionibacterium acnes ( P. acnes ). This study aimed to evaluate the anti-inflammatory effect of micro-current stimulation (MC) on peptidoglycan (PGN)-treated raw 264.7 macrophages and P. acnes -induced skin inflammation. To specify the intensity with anti-inflammatory effects, nitric oxide (NO) production was compared according to various levels of MC. As the lowest NO production was shown at an intensity of 50 μA, subsequent experiments used this intensity. The changes of expression of the proteins related to TLR2/NF-κB signaling were examined by immunoblotting. Also, immunofluorescence analysis was performed for observing NF-κB p65 localization. All of the expression levels of proteins regarding TLR2/NF-κB signaling were decreased by the application of MC. Moreover, the application of MC to PGN-treated raw 264.7 cells showed a significant decrease in the amount of nuclear p65-protein. In the case of animal models with P. acnes -induced skin inflammation, various pro-inflammatory cytokines and mediators significantly decreased in MC-applied mice. In particular, the concentration of IL-1β in serum decreased, and the area of acne lesions, decreased from the histological analysis. We suggest for the first time that MC can be a novel treatment for acne.
Keyphrases
- signaling pathway
- oxidative stress
- diabetic rats
- induced apoptosis
- pi k akt
- nuclear factor
- lps induced
- inflammatory response
- high glucose
- toll like receptor
- nitric oxide
- anti inflammatory
- poor prognosis
- immune response
- drug induced
- cell cycle arrest
- epithelial mesenchymal transition
- soft tissue
- hidradenitis suppurativa
- binding protein
- endothelial cells
- wound healing
- metabolic syndrome
- long non coding rna
- smoking cessation
- bacillus subtilis