Multi-target mechanisms of Bojungikki-tang in psoriasis-like dermatitis: Integrative network and transcriptomic analysis
Year: 2025
Type: article
Abstract: BACKGROUND: Psoriasis is a chronic and complex disease characterized by itching, burning, and soreness with scaly plaques and erythematous lesions. It is associated with various comorbidities, such as rheumatoid arthritis, cardiovascular disease, and psychiatric complications. Psoriasis is a systemic inflammatory disease that increases the release of pro-inflammatory cytokines from chronically-activated innate and adaptive immune systems. To treat multifactorial and complex diseases, system-oriented drug design and drug combinations for synergistic effects are highly effective and advantageous. Previous studies have revealed the immunomodulatory effects of Bojungikki-tang (BJT, Buzhong-Yiqi-Tang in traditional Chinese medicine and Hochu-ekki-to in Kampo medicine) in complex diseases; however, the effect of BJT on psoriasis, a chronic autoimmune disease, has not been evaluated. PURPOSE: We evaluated the effect of BJT against psoriasis and the underlying mechanisms. METHODS: The anti-psoriatic effects of BJT were evaluated in vivo, and the underlying mechanisms were elucidated through network analysis, transcriptomics, UPLC-ESI-MS/MS, and molecular docking. RESULTS: production, and keratinocyte proliferation. Moreover, BJT regulated the expression of PLA2G4D, an enzyme of the arachidonic acid (AA) pathway, as well as other enzymes involved in this pathway, including COX-2. CONCLUSION: This study demonstrated that BJT ameliorated psoriasis-like inflammation by concurrently regulating pivotal pro-inflammatory cytokines and two distinct steps of the AA pathway, which may be related to its multi-component composition. These findings indicate the therapeutic potential of the multi-component drug BJT on multiple targets for psoriasis-like inflammation.
Source: Phytomedicine
Authors: Yun Hee Kim, Hye Jin Kim, Hyun-Kyung Song, Youn-Hwan Hwang, Yu Jin Kim, Seol Jang, Bu-Yeo Kim, Taesoo Kim
Language: English
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $3,630
Award: G7693124976
OpenAlex ID: W4416757687
