脂多糖引起的慢性神经炎症导致小鼠行为障碍

M. Ghasemi-Kasman, Nahid Davoodian
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摘要

背景:有证据表明慢性神经炎症参与神经退行性疾病的发病机制,包括阿尔茨海默病和帕金森病。在这方面,动物模型被认为是研究与这些疾病相关的神经炎症的重要工具。在动物模型中,注射脂多糖(LPS)是最常用的诱导神经炎症的方法。然而,关于长期服用LPS对行为参数的影响的研究有限且不一致。因此,本实验研究旨在比较两种不同剂量慢性注射LPS对小鼠空间学习和工作记忆等行为改变的影响。方法:采用雄性BALB/c小鼠36只。适应1周后,随机分为3组。对照组小鼠连续7天腹腔注射生理盐水,第二组小鼠连续1周注射250 μg/kg的LPS (IP)。最后,第三组小鼠给予750 μg/kg LPS (IP)溶解于生理盐水中,持续1周。采用Morris水迷宫和y型迷宫分别评估小鼠空间学习和工作记忆的变化。结果:基于Y-maze和MWM实验结果发现,高剂量(750 μg/kg) LPS可导致大鼠工作记忆障碍(P=0.0024)和认知功能障碍(P=0.0030)。结论:lps诱导的慢性神经炎症模型可作为研究神经退行性疾病的病理机制和开发新的药物治疗方案的重要工具。
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Chronic Neuroinflammation Induced by Systemic Administration of Lipopolysaccharide Leads to Behavioral Impairments in Mice
Background: There is evidence that chronic neuroinflammation is involved in the pathogenesis of neurodegenerative disorders, including Alzheimer’s and Parkinson’s diseases. In this regard, animal models are considered important tools for the study of neuroinflammation associated with these diseases. The injection of lipopolysaccharide (LPS) is the most commonly used approach for inducing neuroinflammation in animal models. However, there are limited and inconsistent studies regarding the effect of the chronic administration of LPS on behavioral parameters. Accordingly, this experimental study aimed to compare the effect of the chronic injection of LPS in two different doses on behavioral alterations, including spatial learning and working memory in mice. Methods: Thirty-six male BALB/c mice were used in this study. After acclimatization for a week, mice were randomly divided into three groups. Control mice were intraperitoneally (IP) injected with saline for seven consecutive days, and mice of the second group received 250 μg/kg LPS (IP) dissolved in saline for a week. Finally, mice of the third group were administered 750 μg/kg LPS (IP) dissolved in saline for a week. Morris water maze (MWM) and Y-maze were performed to assess spatial learning and working memory alterations in treated mice, respectively. Results: It was found that LPS treatment with a high dose (750 μg/kg) results in working memory impairment (P=0.0024) and cognitive dysfunction (P=0.0030) based on Y-maze and MWM test results. Conclusion: Our findings suggest that the LPS-induced model of chronic neuroinflammation can be used as an important tool for the investigation of the pathomechanisms of neurodegenerative disorders and the development of new pharmacotherapeutic options.
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