A Localized Aldara (5% Imiquimod)–Induced Psoriasiform Dermatitis Model in Mice Using Finn Chambers

Q2 Pharmacology, Toxicology and Pharmaceutics
Szabina Horváth, Ágnes Kemény, Erika Pintér, Rolland Gyulai
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引用次数: 6

Abstract

The expanding number of research studies utilizing the imiquimod-induced psoriasiform dermatitis model attests to the usefulness of this procedure. Advantages of this model include rapid development of the skin response and cost-effectiveness. A major limitation is that application of imiquimod cream over large areas of skin, as well as licking and ingestion of the cream, may lead to severe systemic inflammation, which can cause a general decline in health, splenomegaly, and death. In this protocol, Finn chambers are used to localize the imiquimod cream to a small area of the skin. This results in production of severe and reproducible psoriatic skin reactions with significantly less imiquimod, greatly reducing the possibility of untoward systemic effects. Moreover, having psoriasiform and control skin areas on the same mice decreases inter-animal differences. The protocol can be readily adapted for other skin disease models involving topical application of test agents. This article also details functional measurements performed during assays, including skin thickness, blood perfusion, semiquantitative histopathological evaluation, determination of scaling score to monitor psoriatic symptoms, and collection of spleen and body weight data to identify systemic effects. © 2020 The Authors.

Basic Protocol: Use of Finn chambers to induce psoriasiform skin reactions with imiquimod

Support Protocol 1: Measurement of double-fold dorsal skin thickness

Support Protocol 2: Measurement of blood perfusion

Support Protocol 3: Determination of scaling score

Support Protocol 4: Semiquantitative histopathological scoring

Support Protocol 5: Assessment of systemic side effects in response to imiquimod application

Abstract Image

局部Aldara(5%咪喹莫特)诱导小鼠银屑病样皮炎Finn Chambers模型
越来越多的研究利用吡喹莫德诱导的银屑病样皮炎模型证明了这一程序的有效性。这种模式的优点包括皮肤反应的快速发展和成本效益。一个主要的限制是咪喹莫特乳膏大面积涂抹皮肤,以及舔舐和摄入乳膏,可能导致严重的全身炎症,这可能导致健康状况普遍下降、脾肿大和死亡。在本方案中,芬氏腔用于将咪喹莫特乳膏定位到皮肤的一小块区域。这导致产生严重和可重复的银屑病皮肤反应,显著减少咪喹莫特,大大降低了不良全身效应的可能性。此外,在同一只小鼠身上具有牛皮癣状和对照皮肤区域可以减少动物间的差异。该方案可以很容易地适用于涉及局部应用试验剂的其他皮肤病模型。本文还详细介绍了在检测过程中进行的功能测量,包括皮肤厚度、血液灌注、半定量组织病理学评估、测定评分以监测银屑病症状,以及收集脾脏和体重数据以确定全身效应。©2020作者。基本方案:使用芬氏腔诱导咪喹莫特银屑病样皮肤反应支持方案1:测量双背皮肤厚度支持方案2:测量血液灌注支持方案3:测定评分支持方案4:半定量组织病理学评分支持方案5:评估咪喹莫特应用后的全身副作用
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来源期刊
Current Protocols in Pharmacology
Current Protocols in Pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
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