Chlorogenic Acid Isomers Isolated from Artemisia lavandulaefolia Exhibit Anti-Rosacea Effects In Vitro

• Published in: Biomedicines 2022-02, Vol.10 (2), p.463
• Main Authors: Roh, Kyung-Baeg, Jang, Youngsu, Cho, Eunae, Park, Deokhoon, Kweon, Dae-Hyuk, Jung, Eunsun
• Format: Article
• Language: English
• Subjects: Acids; Angiogenesis; Artemisia lavandulaefolia; Bioactive compounds; cathelicidin; Cell culture; Cell proliferation; Chemokines; Chlorogenic acid; chlorogenic acid isomers; Cytokines; Endothelial cells; Erythema; Immune response; Inflammation; Inflammatory diseases; Isomers; Kallikrein; kallikrein 5; Leukocyte migration; Macrophages; Mast cells; Metabolites; Molecular modelling; Pathophysiology; Peptides; Proteins; Rosacea; Serine proteinase; Skin; Skin diseases; Stratum corneum
• ISSN: 2227-9059; 2227-9059
• DOI: 10.3390/biomedicines10020463

Rosacea is a chronic inflammatory disease affecting facial skin. It is associated with immune and vascular dysfunction mediated via increased expression and activity of cathelicidin and kallikrein 5 (KLK5), a serine protease of stratum corneum. Therefore, KLK5 inhibitors are considered as therapeutic agents for improving the underlying pathophysiology and clinical manifestation of rosacea. Here, we isolated the active constituents of ( ) and investigated their inhibitory effect on KLK5 protease activity. Using bioassay-guided isolation, two bioactive compounds including chlorogenic acid isomers, 3,5-dicaffeoylquinic acid (isochlorogenic acid A) (1), and 4,5-dicaffeoylquinic acid (isochlorogenic acid C) (2) were isolated from . In this study, we evaluated the effects of isochlorogenic acids A and C on dysregulation of vascular and immune responses to rosacea, and elucidated their molecular mechanisms of action. The two chlorogenic acid isomers inhibit KLK5 protease activity, leading to reduced conversion of inactive cathelicidin into active LL-37. This inhibition of LL-37 production by isochlorogenic acids A and C reveals the efficacy of suppressing the expression of inflammatory mediators induced by LL-37 in immune cells such as macrophages and mast cells. In addition, both isomers of chlorogenic acid directly inhibited the proliferation and migration of vascular endothelial cells induced by LL-37.