영문 초록 원문 (PubMed Abstract) 펼쳐보기 ↓
BACKGROUND: Psoriasis is a chronic inflammatory skin disease often referred to as the "incurable cancer," characterized by a long disease course, high recurrence rate, and inability to achieve complete cure. It not only severely impacts patients' quality of life but also faces challenges such as high treatment costs and side effects with current therapeutic approaches. The primary active component of pine pollen (PP) extract (PPE) is dihydroquercetin (DHQ), which possesses various pharmacological activities, including anti-inflammatory, antioxidant, and immune-modulating effects. To date, however, the pharmacological properties and mechanism of action of DHQ remain uncharacterised, and further evidence is required to substantiate its efficacy in treating psoriasis. OBJECTIVE: This study sought to examine the anti-psoriatic properties of PPE, determine its principal active component, and clarify its mechanisms of action along with its therapeutic prospects. METHOD: This study elucidated the anti-psoriatic mechanism of PPE. Bioactivity-directed purification afforded a PPE enriched with DHQ. Subsequent phytochemical analysis employing UPLC-Q-Orbitrap/MS and HPLC identified DHQ and 17 additional active constituents. The mechanism of action was predicted through an integration of network pharmacology and molecular docking, with predictions subsequently validated by RT-qPCR. In LPS-induced RAW 264.7 macrophages, a 24-hour intervention with PPE modulated levels of ROS, apoptosis, mitochondrial membrane potential, cell migration, and inflammatory responses. In a 5 % IMQ-induced murine psoriasis model, seven-day oral administration of PPE conferred therapeutic efficacy, as assessed by PASI scoring, histological and immunohistochemical examination, ELISA, and Western blot analysis. RESULTS: PPE treatment significantly reduced PASI scores, skin thickness, splenic index, and inflammatory cell infiltration. It also reversed intestinal barrier damage, ameliorated small intestinal villus atrophy, and suppressed serum levels of inflammatory cytokines. PPE alleviated psoriasis by inhibiting macrophage-driven inflammation. Integrated UPLC-Q-Orbitrap/MS and HPLC analyses, combined