瘦素对APP/PS1阿尔茨海默病小鼠模型的神经保护作用:小胶质细胞和神经炎症的作用。

IF 2.1 Q3 CLINICAL NEUROLOGY Degenerative neurological and neuromuscular disease Pub Date : 2023-10-25 eCollection Date: 2023-01-01 DOI:10.2147/DNND.S427781
Jing Ma, Yi-Hui Hou, Zhe-Yan Liao, Zheng Ma, Xiao-Xuan Zhang, Jian-Li Wang, Yun-Bo Zhu, Hai-Lei Shan, Ping-Yue Wang, Cheng-Bo Li, Ying-Lei Lv, Yi-Lan Wei, Jie-Zhi Dou
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引用次数: 0

摘要

背景:多年前,小胶质细胞与阿尔茨海默病(AD)密切相关;然而,AD的病理机制尚不清楚。本研究的目的是确定瘦素是否影响年轻和老年雄性APP/PS1小鼠海马中的小胶质细胞。目的:在AD转基因模型中,我们研究了腹膜内注射瘦素与小胶质细胞之间的关系。方法:每天腹腔注射瘦素(1mg/kg),连续1周,分析成年(6个月)和老年(12个月)APP/PS1小鼠海马小胶质细胞的炎症标志物。结果:瘦素治疗组大鼠脑Aβ水平均明显下降。我们发现成年小鼠海马中IL-1β、IL-6和小胶质细胞活化水平增加。使用老年小鼠作为慢性神经炎症和瘦素抵抗的实验模型,与成年小鼠相比,海马中Iba-1+小胶质细胞的数量和IL-1β/IL-6的水平显著增加。但瘦素治疗组和未治疗组之间无差异。结论:瘦素信号传导可调节小胶质细胞的活化和炎症因子的释放,但它并不是AD发病机制中神经保护作用的唯一潜在机制。
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Neuroprotective Effects of Leptin on the APP/PS1 Alzheimer's Disease Mouse Model: Role of Microglial and Neuroinflammation.

Background: Microglia are closely linked to Alzheimer's disease (AD) many years ago; however, the pathological mechanisms of AD remain unclear. The purpose of this study was to determine whether leptin affected microglia in the hippocampus of young and aged male APP/PS1 mice.

Objective: In a transgenic model of AD, we investigated the association between intraperitoneal injection of leptin and microglia.

Methods: We intraperitoneal injection of leptin (1mg/kg) every day for one week and analyzed inflammatory markers in microglia in the hippocampus of adult (6 months) and aged (12 months) APP/PS1 mice.

Results: In all leptin treatment group, the brain Aβ levels were decrease. We found increased levels of IL-1β, IL-6 and microglial activation in the hippocampus of adult mice. Using aged mice as an experimental model for chronic neuroinflammation and leptin resistance, the number of Iba-1+ microglia and the levels of IL-1β/IL-6 in the hippocampus were greatly increased as compared to the adult. But between the leptin treatment and un-treatment, there were no difference.

Conclusion: Leptin signaling would regulate the activation of microglia and the release of inflammatory factors, but it is not the only underlying mechanism in the neuroprotective effects of AD pathogenesis.

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