Developing Monosodium Urate Monohydrate Crystals–Induced Gout Model in Rodents and Rabbits
Yufang Wang, Ya Zhang, Zhengrong Yu, Yige Bai, Mengxing Zhu, Yan Lei, Baoli Dong, Qiyao Zhang, Qingyang Gu, Jian Xiang
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引用次数: 0
Abstract
Gout is a chronic disease caused by the deposition of monosodium urate monohydrate (MSU) crystals within the body, particularly in one or more joints, which can lead to sudden severe attacks of pain, swelling, redness, and tenderness, known as gout flares. Historically termed the “disease of kings,” gout is one of the oldest joint diseases and remains the most common form of inflammatory arthritis haunting humans in the 21st century. It is associated with cardiovascular, metabolic, and renal comorbidities and can lead to reduced mobility and impaired physical function and contributing to work absenteeism. Given its increasing global incidence, novel therapies for gouty arthritis disease are urgently needed. Experimental gout models are indispensable tools for deciphering disease pathogenesis and evaluating the efficacy and side effect of newly developed therapeutics at preclinical stage. Herein, we described a series of highly reproducible acute gout flare and air pouch models in rodents and rabbits that can be used to address various scientific questions relevant to pathological changes and immune responses during and after a gout attack. Animal gout flare models, elicited by MSU crystals, mimic the main histopathological features of human gouty arthritis, including damage to cartilage and joint swelling. Meanwhile, air pouch models serve as a tool to evaluate robust inflammatory cytokine secretion and neutrophil infiltration. This article provides a detailed description of procedures and troubleshooting tips required to reproducibly induce gout flare and air pouch models in animals and critically evaluate the pathogenesis of the disease. © 2025 Wiley Periodicals LLC.
Basic Protocol 1: Preparation of monosodium urate crystalline
Basic Protocol 2: Development of MSU-induced gout flare model in mice
Support Protocol 1: Histological assessment of mouse ankle tissues
Basic Protocol 3: Development of MSU-induced gout flare model in rats
Basic Protocol 4: Development of MSU-induced gout flare model in rabbits
Basic Protocol 5: Development and validation of reference articles in MSU-induced air pouch model in rats
Basic Protocol 6: Development and validation of reference articles in MSU-induced air pouch model in mice
Support Protocol 2: Flow cytometry of mouse neutrophils in air pouch lavage samples
一水合尿酸钠晶体致鼠兔痛风模型的建立
痛风是一种慢性疾病,由一水尿酸单钠(MSU)结晶在体内沉积引起,尤其是在一个或多个关节中,可导致疼痛、肿胀、发红和触痛的突然剧烈发作,即痛风发作。痛风在历史上被称为 "王者之病",是最古老的关节疾病之一,在 21 世纪仍然是困扰人类最常见的炎症性关节炎。痛风与心血管、代谢和肾脏等并发症有关,可导致行动不便和身体功能受损,并造成缺勤。鉴于痛风性关节炎在全球的发病率越来越高,因此迫切需要新型疗法来治疗痛风性关节炎疾病。痛风实验模型是破译疾病发病机制以及在临床前阶段评估新开发疗法的疗效和副作用不可或缺的工具。在这里,我们描述了一系列在啮齿类动物和兔子身上建立的可高度重复的急性痛风发作和气囊模型,这些模型可用于解决痛风发作期间和之后的病理变化和免疫反应方面的各种科学问题。动物痛风发作模型由MSU晶体诱发,可模拟人类痛风性关节炎的主要组织病理学特征,包括软骨损伤和关节肿胀。同时,气囊模型可作为评估炎症细胞因子分泌和中性粒细胞浸润情况的工具。本文详细介绍了在动物中重复诱导痛风发作和气囊模型所需的程序和故障排除技巧,并对该病的发病机制进行了批判性评估。© 2025 Wiley Periodicals LLC.基本方案 1:制备尿酸单钠结晶基本方案 2:建立 MSU 诱导的小鼠痛风发作模型支持方案 1:小鼠踝关节组织的组织学评估基本方案 3:建立 MSU 诱导的大鼠痛风发作模型基本方案 4:建立 MSU 诱导的大鼠痛风发作模型支持性实验 2:气囊灌洗样本中小鼠中性粒细胞的流式细胞仪测定
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