A derivative of tanshinone IIA and salviadione, 15a, inhibits inflammation and alleviates DSS-induced colitis in mice by direct binding and inhibition of RIPK2.

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Tác giả: Yue Chen, Chun-Yong Ding, Cheng-Hong Hu, Bo Jin, Tian-Yang Jin, Guang Liang, Jing Liao, Fang-Min Ning, Wei-Yang Tang, Yi Wang, Zhe Wang, Xiao-Hong Wei, Lei-Yu Xu, Ao Zhang, Ling-Xi Zhang

Ngôn ngữ: eng

Ký hiệu phân loại: 296.45047 Traditions, rites, public services

Thông tin xuất bản: United States : Acta pharmacologica Sinica , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 251641

Inflammatory bowel diseases (IBDs) are chronic inflammatory conditions primarily affecting the gastrointestinal tract. Previous studies established the role of the NF-κB signaling pathway in the development of IBDs, suggesting that anti-inflammatory therapies might offer a viable treatment strategy. Tanshinone IIA and salviadione, both derived from Salviae Miltiorrhizae Radix et Rhizoma, possess anti-inflammatory and anti-oxidative activities. A series of new compounds were synthesized by hybridizing salviadione with tanshinone. Among these compounds, 15a showed beneficial effects in LPS-induced acute lung injury and diabetes-induced renal injury mouse models. The current study explored the therapeutic efficacy of 15a using both acute and chronic colitis models and elucidated the underlying mechanisms. DSS-induced colitis models were established in mice, where acute colitis was treated with compound 15a (5 or 10 mg·kg
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