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本文引用的文献

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The NF-κB signaling system in the immunopathogenesis of inflammatory bowel disease.炎症性肠病免疫发病机制中的核因子κB信号系统
Sci Signal. 2024 Jan 9;17(818):eadh1641. doi: 10.1126/scisignal.adh1641.
2
Receptor-interacting protein kinase 2 (RIPK2) profoundly contributes to post-stroke neuroinflammation and behavioral deficits with microglia as unique perpetrators.受体相互作用蛋白激酶 2(RIPK2)通过小胶质细胞作为独特的执行者,对卒中后神经炎症和行为缺陷有深远影响。
J Neuroinflammation. 2023 Sep 30;20(1):221. doi: 10.1186/s12974-023-02907-6.
3
Discovery of a novel RIPK2 inhibitor for the treatment of inflammatory bowel disease.发现一种新型 RIPK2 抑制剂,可用于治疗炎症性肠病。
Biochem Pharmacol. 2023 Aug;214:115647. doi: 10.1016/j.bcp.2023.115647. Epub 2023 Jun 12.
4
Recent advances in the development of RIPK2 modulators for the treatment of inflammatory diseases.用于治疗炎症性疾病的RIPK2调节剂开发的最新进展。
Front Pharmacol. 2023 Mar 7;14:1127722. doi: 10.3389/fphar.2023.1127722. eCollection 2023.
5
Pathophysiology of Inflammatory Bowel Disease: Innate Immune System.炎症性肠病的病理生理学:固有免疫系统。
Int J Mol Sci. 2023 Jan 12;24(2):1526. doi: 10.3390/ijms24021526.
6
Inflammatory Bowel Disease: A Review of Pre-Clinical Murine Models of Human Disease.炎症性肠病:人类疾病的临床前小鼠模型综述。
Int J Mol Sci. 2022 Aug 19;23(16):9344. doi: 10.3390/ijms23169344.
7
Melatonin mitigates aflatoxin B1-induced liver injury via modulation of gut microbiota/intestinal FXR/liver TLR4 signaling axis in mice.褪黑素通过调节肠道微生物群/肠道 FXR/肝脏 TLR4 信号轴减轻黄曲霉毒素 B1 诱导的小鼠肝损伤。
J Pineal Res. 2022 Sep;73(2):e12812. doi: 10.1111/jpi.12812. Epub 2022 Jun 12.
8
The Gut Microbiota in Inflammatory Bowel Disease.肠道微生物群与炎症性肠病。
Front Cell Infect Microbiol. 2022 Feb 22;12:733992. doi: 10.3389/fcimb.2022.733992. eCollection 2022.
9
The influence of cytokines on the complex pathology of ulcerative colitis.细胞因子对溃疡性结肠炎复杂病理学的影响。
Autoimmun Rev. 2022 Mar;21(3):103017. doi: 10.1016/j.autrev.2021.103017. Epub 2021 Dec 10.
10
RIPK2 as a New Therapeutic Target in Inflammatory Bowel Diseases.RIPK2作为炎症性肠病的新治疗靶点
Front Pharmacol. 2021 Apr 14;12:650403. doi: 10.3389/fphar.2021.650403. eCollection 2021.

丹参酮IIA和丹参二酮的衍生物15a通过直接结合并抑制RIPK2来抑制炎症并减轻小鼠的右旋糖酐硫酸钠诱导的结肠炎。

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

作者信息

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

机构信息

School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, China.

Chemical Biology Research Center, Wenzhou Medical University, School of Pharmaceutical Sciences, Wenzhou, 325035, China.

出版信息

Acta Pharmacol Sin. 2025 Mar;46(3):672-686. doi: 10.1038/s41401-024-01399-1. Epub 2024 Oct 23.

DOI:10.1038/s41401-024-01399-1
PMID:39443729
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11845706/
Abstract

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·d) for 8 days, while chronic colitis mice received compound 15a (5 or 10 mg·kg·d, i.g.) during 2.5% DSS administration. The 15a treatment significantly alleviated DSS-induced pathological and inflammatory damages in both acute and chronic colitis mouse models. In mouse intestinal epithelial cell line MODE-K, pretreatment with compound 15a (5 or 10 μM) significantly suppressed LPS + L18-MDP-induced inflammatory responses. The receptor-interacting serine/threonine kinase 2 (RIPK2) was identified as a direct binding target of compound 15a using microarrays and recombinant human proteins. Moreover, 15a could directly bind to and inhibit the phosphorylation of RIPK2, leading to the suppression of the NF-κB and MAPK signaling pathways. Furthermore, LEU153 and VAL32 were identified within the KD domain of RIPK2 as critical amino residues for the binding of 15a. Briefly, the current findings demonstrate that compound 15a holds promise as a therapeutic agent for managing acute and chronic colitis.

摘要

炎症性肠病(IBDs)是主要影响胃肠道的慢性炎症性疾病。先前的研究确定了NF-κB信号通路在IBDs发病中的作用,提示抗炎治疗可能是一种可行的治疗策略。丹参酮IIA和丹参二酮均来源于丹参,具有抗炎和抗氧化活性。通过将丹参二酮与丹参酮杂交合成了一系列新化合物。在这些化合物中,15a在脂多糖诱导的急性肺损伤和糖尿病诱导的肾损伤小鼠模型中显示出有益作用。本研究使用急性和慢性结肠炎模型探索了15a的治疗效果,并阐明了其潜在机制。在小鼠中建立了葡聚糖硫酸钠(DSS)诱导的结肠炎模型,急性结肠炎用化合物15a(5或10mg·kg·d)治疗8天,而慢性结肠炎小鼠在给予2.5% DSS期间接受化合物15a(5或10mg·kg·d,腹腔注射)。15a治疗显著减轻了急性和慢性结肠炎小鼠模型中DSS诱导的病理和炎症损伤。在小鼠肠上皮细胞系MODE-K中,用化合物15a(5或10μM)预处理可显著抑制脂多糖+L18-MDP诱导的炎症反应。使用微阵列和重组人蛋白鉴定出受体相互作用丝氨酸/苏氨酸激酶2(RIPK2)是化合物15a的直接结合靶点。此外,15a可直接结合并抑制RIPK2的磷酸化,导致NF-κB和丝裂原活化蛋白激酶(MAPK)信号通路的抑制。此外,在RIPK2的KD结构域内鉴定出亮氨酸153和缬氨酸32是15a结合的关键氨基酸残基。简而言之,目前的研究结果表明化合物15a有望成为治疗急性和慢性结肠炎的药物。