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大鼠Ⅰ型复杂性区域疼痛综合征的慢性缺血后疼痛模型

Chronic Post-Ischemia Pain Model for Complex Regional Pain Syndrome Type-I in Rats.

作者信息

Hu Qimiao, Zheng Xiaoli, Chen Ruixiang, Liu Boyu, Tai Yan, Shao Xiaomei, Fang Jianqiao, Liu Boyi

机构信息

Department of Neurobiology and Acupuncture Research, The Third Clinical Medical College, Zhejiang Chinese Medical University, Key Laboratory of Acupuncture and Neurology of Zhejiang Province.

Academy of Chinese Medical Sciences, Zhejiang Chinese Medical University.

出版信息

J Vis Exp. 2020 Jan 21(155). doi: 10.3791/60562.

Abstract

Complex regional pain syndrome type-I (CRPS-I) is a neurological disease that causes severe pain among patients and remains an unresolved medical condition. However, the underlying mechanisms of CRPS-I have yet to be revealed. It is known that ischemia/reperfusion is one of the leading factors that causes CRPS-I. By means of prolonged ischemia and reperfusion of the hind limb, the rat chronic post-ischemia pain (CPIP) model has been established to mimic CRPS-I. The CPIP model has become a well-recognized animal model for studying the mechanisms of CRPS-I. This protocol describes the detailed procedures involved in the establishment of the rat model of CPIP, including anesthesia, followed by ischemia/reperfusion of the hind limb. Characteristics of the rat CPIP model are further evaluated by measuring the mechanical and thermal hypersensitivities of the hind limb as well as the nocifensive responses to acute capsaicin injection. The rat CPIP model exhibits several CRPS-I-like manifestations, including hind limb edema and hyperemia in the early stage after establishment, persistent thermal and mechanical hypersensitivities, and increased nocifensive responses to acute capsaicin injection. These characteristics render it a suitable animal model for further investigation of the mechanisms involved in CRPS-I.

摘要

I型复杂性区域疼痛综合征(CRPS-I)是一种导致患者严重疼痛的神经系统疾病,至今仍是一个尚未解决的医学问题。然而,CRPS-I的潜在机制尚未明确。已知缺血/再灌注是导致CRPS-I的主要因素之一。通过对后肢进行长时间的缺血和再灌注,建立了大鼠慢性缺血后疼痛(CPIP)模型来模拟CRPS-I。CPIP模型已成为研究CRPS-I机制的公认动物模型。本方案描述了建立大鼠CPIP模型所涉及的详细步骤,包括麻醉,随后进行后肢的缺血/再灌注。通过测量后肢的机械和热超敏反应以及对急性辣椒素注射的伤害性反应,进一步评估大鼠CPIP模型的特征。大鼠CPIP模型表现出几种类似CRPS-I的表现,包括建立模型后早期的后肢水肿和充血、持续的热和机械超敏反应以及对急性辣椒素注射的伤害性反应增加。这些特征使其成为进一步研究CRPS-I相关机制的合适动物模型。

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