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本文引用的文献

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Deficiency of histone deacetylases 3 in macrophage alleviates monosodium urate crystals-induced gouty inflammation in mice.组蛋白去乙酰化酶 3 在巨噬细胞中的缺乏可减轻尿酸单钠晶体诱导的小鼠痛风性炎症。
Arthritis Res Ther. 2024 May 6;26(1):96. doi: 10.1186/s13075-024-03335-4.
2
Protocol to create a murine subcutaneous air pouch for the study of monosodium urate crystal-induced gout.建立用于研究单钠尿酸盐晶体诱导痛风的小鼠皮下气囊的方案。
STAR Protoc. 2024 Mar 15;5(1):102888. doi: 10.1016/j.xpro.2024.102888. Epub 2024 Feb 13.
3
Neutrophil autophagy induced by monosodium urate crystals facilitates neutrophil extracellular traps formation and inflammation remission in gouty arthritis.尿酸单钠晶体诱导中性粒细胞自噬促进痛风性关节炎中性粒细胞胞外诱捕网形成和炎症缓解。
Front Endocrinol (Lausanne). 2023 Sep 22;14:1071630. doi: 10.3389/fendo.2023.1071630. eCollection 2023.
4
Comparison of the different monosodium urate crystals in the preparation process and pro-inflammation.比较不同单钠尿酸盐晶体在制备过程中的差异及促炎作用。
Adv Rheumatol. 2023 Aug 8;63(1):39. doi: 10.1186/s42358-023-00307-1.
5
Improved polarized light microscopic detection of gouty crystals via dissolution with formalin and ethylenediamine tetraacetic acid.通过甲醛和乙二胺四乙酸溶解提高痛风晶体的偏光显微镜检测。
Sci Rep. 2023 May 9;13(1):7505. doi: 10.1038/s41598-023-34570-5.
6
Biomineralized Nanoscavenger Abrogates Proinflammatory Macrophage Polarization and Induces Neutrophil Clearance through Reverse Migration during Gouty Arthritis.生物矿化纳米清除剂通过痛风性关节炎中的反向迁移来消除促炎型巨噬细胞极化并诱导中性粒细胞清除
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7
Potential anti-gout properties of Wuwei Shexiang pills based on network pharmacology and pharmacological verification.基于网络药理学和药效学验证的五味麝香丸潜在抗痛风作用研究
J Ethnopharmacol. 2023 Apr 6;305:116147. doi: 10.1016/j.jep.2023.116147. Epub 2023 Jan 3.
8
The Burden of Gout and Its Attributable Risk Factors in the Middle East and North Africa Region, 1990 to 2019.1990年至2019年中东和北非地区痛风负担及其可归因风险因素
J Rheumatol. 2023 Jan;50(1):107-116. doi: 10.3899/jrheum.220425. Epub 2022 Sep 1.
9
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10
Models of Inflammation: Carrageenan Air Pouch.炎症模型:角叉菜胶气囊。
Curr Protoc. 2021 Aug;1(8):e183. doi: 10.1002/cpz1.183.

使用尿酸钠和焦磷酸钙的皮下气囊模型的系统评价及研究晶体相关性关节病的建议

Systematic review of the subcutaneous air pouch model using monosodium urate and calcium pyrophosphate and recommendations for studying crystal-related arthropathies.

作者信息

Hewage Wenu, Vidimce Josif, Shiels Ryan G, Morgan Michael, Bulmer Andrew C

机构信息

School of Pharmacy and Medical Science, Griffith University, Gold Coast, Queensland, Australia.

School of Medicine and Dentistry, Griffith University, Gold Coast, Queensland, Australia.

出版信息

Animal Model Exp Med. 2025 Sep;8(9):1611-1627. doi: 10.1002/ame2.70058. Epub 2025 Jul 11.

DOI:10.1002/ame2.70058
PMID:40641359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12531122/
Abstract

The subcutaneous air pouch model has been used extensively to study the pathophysiology of inflammatory conditions such as joint diseases and the potential efficacy of pharmacological treatments in vivo. Delivery of air between the subcutaneous and dermal layer of the intra-scapular zone of the rodent generates an environment analogous to the synovial joint space. Introduction of monosodium urate crystals or calcium pyrophosphate crystals into the air space produces a sterile acute inflammatory response mimicking clinical gout and pseudogout, respectively. The inflammatory response can be quantitatively and robustly evaluated by measuring leukocyte infiltration, inflammatory cytokine production, eicosanoid release, complement activation and reactive oxygen species generation. Despite the utility of this model, great variation exists within the literature regarding the design, sampling time points, and endpoints measured. This systematic review summarizes the current literature on the subcutaneous air pouch model studying monosodium urate or calcium pyrophosphate crystals and provides recommendations for standardizing and improving the reliability and validity of this model. Standardizing the experimental approach would improve inter-study comparability, increase the internal validity of studies and reproducibility of results, and ultimately improve the understanding of gout and pseudogout and accelerate the discovery of new pharmacological therapies.

摘要

皮下气囊模型已被广泛用于研究诸如关节疾病等炎症性疾病的病理生理学以及体内药物治疗的潜在疗效。在啮齿动物肩胛区内的皮下层和真皮层之间注入空气,可产生类似于滑膜关节腔的环境。向气囊内注入尿酸单钠晶体或焦磷酸钙晶体,分别产生模拟临床痛风和假性痛风的无菌性急性炎症反应。通过测量白细胞浸润、炎症细胞因子产生、类花生酸释放、补体激活和活性氧生成,可对炎症反应进行定量且有力的评估。尽管该模型具有实用性,但文献中在设计、采样时间点和测量终点方面存在很大差异。本系统评价总结了目前关于皮下气囊模型研究尿酸单钠或焦磷酸钙晶体的文献,并为规范和提高该模型的可靠性和有效性提供建议。标准化实验方法将提高研究间的可比性,增加研究的内部效度和结果的可重复性,并最终增进对痛风和假性痛风的理解,加速新药理学疗法的发现。