优化脓毒症相关脑病小鼠模型:基于改进的SHIRPA评分和小鼠神经行为的合理标准

IF 4.8 1区 医学 Q1 NEUROSCIENCES
Yuewen Xin, Mi Tian, Xu Pei, Shuixiang Deng, Yao Wang, Feng Zhao, Thomas Behnisch, Yanqin Gao, Ye Gong
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引用次数: 0

摘要

脓毒症相关脑病(SAE)是一种严重的神经系统疾病,以广泛的脑功能障碍为特征。目前,动物模型中SAE的诊断还没有统一的标准。本研究提出了一种标准化的小鼠SAE评估方法,解决了目前研究中的不一致之处。方法采用盲肠结扎和穿刺(CLP)模型诱导脓毒症,我们用改进的SHIRPA评分来评估小鼠的生理状态,以区分SAE和非SAE,通过各种行为测试和神经炎症和神经元损伤评估来验证我们的发现。结果我们的研究结果表明,传统的轻度-中度-重度SHIRPA分类不足以区分SAE和非SAE。为了增强分化,我们根据修正SHIRPA评分中值对小鼠进行分类,并通过y迷宫、三室社会测试和开放场测试等行为测试验证了该方法。该方法有效地鉴定了脓毒症小鼠的神经损伤。进一步的验证包括评估神经元损伤、神经炎症、Morris水迷宫和海马CA1区的长期增强(LTP)。结果表明,与下median组相比,上median组小鼠表现出更大的神经炎症、神经元损伤和认知缺陷。结论本研究建立了一种可靠的SAE小鼠模型评估方法,有助于更好地区分SAE与非SAE。这些进展将增强我们对SAE发病机制的理解,并指导更有效的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Optimized Mouse Model of Sepsis-Associated Encephalopathy: A Rational Standard Based on Modified SHIRPA Score and Neurobehaviors in Mice

Optimized Mouse Model of Sepsis-Associated Encephalopathy: A Rational Standard Based on Modified SHIRPA Score and Neurobehaviors in Mice

Background

Sepsis-associated encephalopathy (SAE), a severe neurological disorder, is marked by widespread brain dysfunction. At present, there is no universally accepted criterion for diagnosing SAE in animal models. This study proposes a standardized evaluation method for SAE in mice, addressing inconsistencies in current research.

Method

Using a cecal ligation and puncture (CLP) model to induce sepsis, we assessed the physiological status of mice with a modified SHIRPA score to differentiate SAE from non-SAE, validating our findings through various behavioral tests and evaluations of neuroinflammation and neuronal damage.

Results

Our findings revealed that the conventional mild–moderate–severe categorization of SHIRPA was insufficient for distinguishing between SAE and non-SAE. To enhance differentiation, we classified mice based on the median modified SHIRPA score, validating this approach through behavioral tests including the Y-maze, three-chamber social test, and open field test. This method effectively identified neurological impairments in septic mice. Further validation involved assessing neuronal damage, neuroinflammation, the Morris water maze, and long-term potentiation (LTP) in the hippocampal CA1 region. Results indicated that mice in the up-Median group exhibited greater neuroinflammation, neuronal injury, and cognitive deficits compared to the down-Median group.

Conclusions

This study establishes a reliable evaluation method for SAE in murine models, facilitating improved differentiation between SAE and non-SAE. Such advancements will enhance our understanding of the pathogenesis of SAE and guide more effective treatment strategies.

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来源期刊
CNS Neuroscience & Therapeutics
CNS Neuroscience & Therapeutics 医学-神经科学
CiteScore
7.30
自引率
12.70%
发文量
240
审稿时长
2 months
期刊介绍: CNS Neuroscience & Therapeutics provides a medium for rapid publication of original clinical, experimental, and translational research papers, timely reviews and reports of novel findings of therapeutic relevance to the central nervous system, as well as papers related to clinical pharmacology, drug development and novel methodologies for drug evaluation. The journal focuses on neurological and psychiatric diseases such as stroke, Parkinson’s disease, Alzheimer’s disease, depression, schizophrenia, epilepsy, and drug abuse.
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