Fermented Taiwanofungus camphoratus Extract Ameliorates Psoriasis-Associated Response in HaCaT Cells via Modulating NF-𝜅B and mTOR Pathways.
Jia-Wei ShenPo-Yuan WuYueh-Hsiung KuoQiao-Xin ChangKuo-Ching WenHsiu-Mei ChiangPublished in: International journal of molecular sciences (2022)
Psoriasis is a chronic autoimmune disease, and until now, it remains an incurable disease. Therefore, the development of new drugs or agents that ameliorate the disease will have marketing potential. Taiwanofungus camphoratus (TC) is a specific fungus in Taiwan. It is demonstrated to have anticancer, anti-inflammation, and hepatoprotective effects. However, the effects of TC fermented extract on psoriasis are under investigation. In this research, we studied the ability of TC on antioxidative activity and the efficacy of TC on interleukin-17 (IL-17A)-induced intracellular oxidative stress, inflammation-relative, and proliferation-relative protein expression in human keratinocytes. The results of a DPPH radical scavenging assay, reducing power assay, and hydroxyl peroxide inhibition assay indicated that TC has a potent antioxidant ability. Furthermore, TC could reduce IL-17A-induced intracellular ROS generation and restore the NADPH level. In the investigation of pathogenesis, we discovered TC could regulate inflammatory and cell proliferation pathways via p -IKKα/ p -p65 and p -mTOR/ p -p70S6k signaling pathways in human keratinocytes. In conclusion, TC showed characteristics such as antioxidant, anti-inflammatory, and anti-psoriatic-associated responses. It is expected to be developed as a candidate for oxidative-stress-induced skin disorders or psoriasis treatment.
Keyphrases
- oxidative stress
- anti inflammatory
- diabetic rats
- induced apoptosis
- signaling pathway
- cell proliferation
- endothelial cells
- dna damage
- high throughput
- drug induced
- reactive oxygen species
- ischemia reperfusion injury
- high glucose
- pi k akt
- multiple sclerosis
- rheumatoid arthritis
- immune response
- systemic lupus erythematosus
- heat shock
- soft tissue
- endoplasmic reticulum stress
- disease activity
- epithelial mesenchymal transition
- climate change
- stress induced
- replacement therapy