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朝着更好的治疗类风湿关节炎的盐酸青藤碱类药物发展:分子机制与结构修饰。

Towards Better Sinomenine-Type Drugs to Treat Rheumatoid Arthritis: Molecular Mechanisms and Structural Modification.

机构信息

School of Medicine, Huanghe Science and Technology College, Zhengzhou 450006, China.

Artemisinin Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China.

出版信息

Molecules. 2022 Dec 7;27(24):8645. doi: 10.3390/molecules27248645.

DOI:10.3390/molecules27248645
PMID:36557779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9781648/
Abstract

Sinomenine is the main component of the vine . It was first isolated in the early 1920s and has since attracted special interest as a potential anti-rheumatoid arthritis (RA) agent, owing to its successful application in traditional Chinese medicine for the treatment of neuralgia and rheumatoid diseases. In the past few decades, significant advances have broadened our understanding of the molecular mechanisms through which sinomenine treats RA, as well as the structural modifications necessary for improved pharmacological activity. In this review, we summarize up-to-date reports on the pharmacological properties of sinomenine in RA treatment, document their underlying mechanisms, and provide an overview of promising sinomenine derivatives as potential RA drug therapies.

摘要

青藤碱是青藤属植物的主要成分。它于 20 世纪 20 年代初首次被分离出来,由于在传统中医中成功地应用于治疗神经痛和类风湿病,青藤碱作为一种潜在的抗类风湿关节炎 (RA) 药物引起了人们的特别关注。在过去的几十年中,重大进展拓宽了我们对青藤碱治疗 RA 的分子机制的理解,以及对改善药理活性所需的结构修饰。在这篇综述中,我们总结了青藤碱在 RA 治疗中的药理学特性的最新报告,记录了它们的潜在机制,并概述了有前途的青藤碱衍生物作为潜在的 RA 药物治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0d3/9781648/7a77bd32c9fd/molecules-27-08645-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0d3/9781648/b9cf61b4315a/molecules-27-08645-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0d3/9781648/a27ce61acf68/molecules-27-08645-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0d3/9781648/7a77bd32c9fd/molecules-27-08645-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0d3/9781648/b9cf61b4315a/molecules-27-08645-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0d3/9781648/a27ce61acf68/molecules-27-08645-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0d3/9781648/7a77bd32c9fd/molecules-27-08645-g003.jpg

相似文献

1
Towards Better Sinomenine-Type Drugs to Treat Rheumatoid Arthritis: Molecular Mechanisms and Structural Modification.朝着更好的治疗类风湿关节炎的盐酸青藤碱类药物发展:分子机制与结构修饰。
Molecules. 2022 Dec 7;27(24):8645. doi: 10.3390/molecules27248645.
2
Anti-inflammatory activities of Chinese herbal medicine sinomenine and Liang Miao San on tumor necrosis factor-α-activated human fibroblast-like synoviocytes in rheumatoid arthritis.中药青藤碱和梁丘散对肿瘤坏死因子-α激活的类风湿关节炎成纤维样滑膜细胞的抗炎作用。
J Ethnopharmacol. 2011 Sep 1;137(1):457-68. doi: 10.1016/j.jep.2011.05.048. Epub 2011 Jun 6.
3
Sinomenine inhibits the inflammatory responses of human fibroblast-like synoviocytes the TLR4/MyD88/NF-κB signaling pathway in rheumatoid arthritis.青藤碱抑制类风湿关节炎中人类成纤维样滑膜细胞的炎症反应及TLR4/MyD88/NF-κB信号通路。
Pharmazie. 2017 Jun 1;72(6):355-360. doi: 10.1691/ph.2017.6946.
4
Sinomenine alleviates mechanical hypersensitivity in mice with experimentally induced rheumatoid arthritis.青藤碱可减轻实验性诱导的类风湿性关节炎小鼠的机械性超敏反应。
Scand J Pain. 2015 Apr 1;7(1):9-14. doi: 10.1016/j.sjpain.2014.12.003.
5
The anti-angiogenic effect of sinomenine.青藤碱的抗血管生成作用。
Angiogenesis. 2005;8(1):3-12. doi: 10.1007/s10456-005-2892-z.
6
Pharmacology of sinomenine, an anti-rheumatic alkaloid from Sinomenium acutum.青藤碱的药理学,一种来自青风藤的抗风湿生物碱。
Acta Med Okayama. 1976 Feb;30(1):1-20.
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Sinomenine ameliorates arthritis via MMPs, TIMPs, and cytokines in rats.青藤碱通过基质金属蛋白酶、基质金属蛋白酶组织抑制剂和细胞因子改善大鼠关节炎。
Biochem Biophys Res Commun. 2008 Nov 14;376(2):352-7. doi: 10.1016/j.bbrc.2008.08.153. Epub 2008 Sep 7.
8
Pharmacological mechanisms of sinomenine in anti-inflammatory immunity and osteoprotection in rheumatoid arthritis: A systematic review.盐酸青藤碱在类风湿关节炎抗炎免疫及护骨中的作用机制:系统评价。
Phytomedicine. 2023 Dec;121:155114. doi: 10.1016/j.phymed.2023.155114. Epub 2023 Sep 27.
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Sinomenine Inhibits the Progression of Rheumatoid Arthritis by Regulating the Secretion of Inflammatory Cytokines and Monocyte/Macrophage Subsets.青藤碱通过调节炎症细胞因子和单核细胞/巨噬细胞亚群的分泌抑制类风湿关节炎的进展。
Front Immunol. 2018 Sep 26;9:2228. doi: 10.3389/fimmu.2018.02228. eCollection 2018.
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Multifunctional nanoparticles of sinomenine hydrochloride for treat-to-target therapy of rheumatoid arthritis via modulation of proinflammatory cytokines.盐酸青藤碱多功能纳米粒通过调节促炎细胞因子实现类风湿关节炎的靶向治疗。
J Control Release. 2022 Aug;348:42-56. doi: 10.1016/j.jconrel.2022.05.016. Epub 2022 Jun 2.

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Research progress in treatment of rheumatoid arthritis with Sinomenine and related formulations based on different administration routes.青藤碱及其不同给药途径相关制剂治疗类风湿关节炎的研究进展
Front Pharmacol. 2025 Aug 6;16:1613679. doi: 10.3389/fphar.2025.1613679. eCollection 2025.
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Overview of mechanisms and novel therapies on rheumatoid arthritis from a cellular perspective.从细胞角度概述类风湿关节炎的发病机制和新型治疗方法。
Front Immunol. 2024 Sep 23;15:1461756. doi: 10.3389/fimmu.2024.1461756. eCollection 2024.
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Revolutionizing rheumatoid arthritis therapy: harnessing cytomembrane biomimetic nanoparticles for novel treatment strategies.

本文引用的文献

1
Synthesis and biological evaluation of novel sinomenine derivatives as anti-inflammatory and analgesic agent.新型青藤碱衍生物作为抗炎和镇痛剂的合成及生物学评价
RSC Adv. 2022 Oct 20;12(46):30001-30007. doi: 10.1039/d2ra05558a. eCollection 2022 Oct 17.
2
Sinomenine increases the methylation level at specific GCG site in mPGES-1 promoter to facilitate its specific inhibitory effect on mPGES-1.青藤碱通过增加 mPGES-1 启动子中特定 GCG 位点的甲基化水平来促进其对 mPGES-1 的特异性抑制作用。
Biochim Biophys Acta Gene Regul Mech. 2022 Apr;1865(3):194813. doi: 10.1016/j.bbagrm.2022.194813. Epub 2022 Apr 10.
3
革新类风湿性关节炎治疗:利用细胞膜仿生纳米颗粒实现新型治疗策略
Drug Deliv Transl Res. 2025 Jan;15(1):66-83. doi: 10.1007/s13346-024-01605-x. Epub 2024 May 17.
4
Lineage-Specific CYP80 Expansion and Benzylisoquinoline Alkaloid Diversity in Early-Diverging Eudicots.早期分化的真双子叶植物中特异性 CYP80 扩张和苄基异喹啉生物碱多样性。
Adv Sci (Weinh). 2024 May;11(19):e2309990. doi: 10.1002/advs.202309990. Epub 2024 Mar 13.
5
Bioactivities and Mechanisms of Action of Sinomenine and Its Derivatives: A Comprehensive Review.青藤碱及其衍生物的生物活性与作用机制:综述
Molecules. 2024 Jan 22;29(2):540. doi: 10.3390/molecules29020540.
6
Akuammiline alkaloid derivatives: divergent synthesis and effect on the proliferation of rheumatoid arthritis fibroblast-like synoviocytes.阿枯米灵生物碱衍生物:发散合成及其对类风湿性关节炎成纤维细胞样滑膜细胞增殖的影响。
Front Chem. 2023 Apr 28;11:1179948. doi: 10.3389/fchem.2023.1179948. eCollection 2023.
Sinomenine inhibits macrophage M1 polarization by downregulating α7nAChR via a feedback pathway of α7nAChR/ERK/Egr-1.
青藤碱通过α7nAChR/ERK/Egr-1的反馈途径下调α7nAChR,从而抑制巨噬细胞M1极化。
Phytomedicine. 2022 Jun;100:154050. doi: 10.1016/j.phymed.2022.154050. Epub 2022 Mar 21.
4
Novel synovial targeting peptide-sinomenine conjugates as a potential strategy for the treatment of rheumatoid arthritis.新型滑膜靶向肽-青藤碱缀合物治疗类风湿关节炎的潜在策略。
Int J Pharm. 2022 Apr 5;617:121628. doi: 10.1016/j.ijpharm.2022.121628. Epub 2022 Mar 1.
5
Targeting MyD88 Downregulates Inflammatory Mediators and Pathogenic Processes in PBMC From DMARDs-Naïve Rheumatoid Arthritis Patients.靶向髓样分化因子88可下调初治类风湿关节炎患者外周血单核细胞中的炎症介质和致病过程。
Front Pharmacol. 2021 Dec 23;12:800220. doi: 10.3389/fphar.2021.800220. eCollection 2021.
6
Understanding the Role and Uses of Alternative Therapies for the Management of Rheumatoid Arthritis.了解替代疗法在类风湿性关节炎管理中的作用和用途。
Curr Rheumatol Rev. 2022;18(2):89-100. doi: 10.2174/1573397117666211116102454.
7
Sinomenine in Cardio-Cerebrovascular Diseases: Potential Therapeutic Effects and Pharmacological Evidences.青藤碱在心血管疾病中的潜在治疗作用及药理学证据
Front Cardiovasc Med. 2021 Oct 1;8:749113. doi: 10.3389/fcvm.2021.749113. eCollection 2021.
8
Sinomenine increases adenosine A receptor and inhibits NF-κB to inhibit arthritis in adjuvant-induced-arthritis rats and fibroblast-like synoviocytes through α7nAChR.青藤碱通过α7烟碱型乙酰胆碱受体增加腺苷A受体并抑制核因子κB,从而抑制佐剂诱导性关节炎大鼠和滑膜成纤维样细胞的关节炎。
J Leukoc Biol. 2021 Dec;110(6):1113-1120. doi: 10.1002/JLB.3MA0121-024RRRR. Epub 2021 Aug 23.
9
C16, a novel sinomenine derivatives, promoted macrophage reprogramming toward M2-like phenotype and protected mice from endotoxemia.C16,一种新型的盐酸青藤碱衍生物,促进巨噬细胞向 M2 样表型重编程,并保护小鼠免受内毒素血症的影响。
Int J Immunopathol Pharmacol. 2021 Jan-Dec;35:20587384211026786. doi: 10.1177/20587384211026786.
10
Chemoproteomics-based target profiling of sinomenine reveals multiple protein regulators of inflammation.基于化学蛋白质组学的青藤碱作用靶点分析揭示了多种炎症相关蛋白调控因子。
Chem Commun (Camb). 2021 Jun 15;57(48):5981-5984. doi: 10.1039/d1cc01522b.