艾灸通过IL-33/ST2途径影响阿尔茨海默病小鼠海马小胶质细胞的极化

Hong-Ying Li, Yuan Shen, Lu-Shuang Xie, Qiao-Feng Wu, Shu-Guang Yu
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The positive expression of amyloid-β (Aβ), phosphorylated Tau (p-Tau), IL-33/ionized calcium binding adapter molecule 1(Iba-1), ST2/Iba-1, arginase 1 (Arg1)/Iba-1 and indu-cible nitric oxide synthase (iNOS)/Iba-1 in hippocampal CA1 region were detected by immunofluorescence.</p><p><strong>Results: </strong>Compared with the control group, the escape latency of the mice in the model group was prolonged (<i>P</i><0.001, <i>P</i><0.01), the number of times to enter the effective area and the percentage of target quadrant swimming time were reduced (<i>P</i><0.001), the positive expression of both Aβ and p-Tau, the positive expression of iNOS/Iba-1 in the hippocampal CA1 region was increased (<i>P</i><0.001), while the expression of IL-33 and ST2 protein in hippocampal tissue, the positive expression levels of IL-33/Iba-1, ST2/Iba-1 and Arg1/Iba-1 in hippocampal CA1 region were all decreased (<i>P</i><0.05, <i>P</i><0.001). 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引用次数: 0

摘要

目的观察艾灸通过白细胞介素-33(IL-33)/生长刺激基因2蛋白(ST2)信号通路对阿尔茨海默病(AD)小鼠小胶质细胞向M2方向极化的影响:将5月龄APP/PS1雄性小鼠随机分为模型组和艾灸组,同龄C57BL/6J小鼠为对照组,每组9只。在灸组中,艾灸 "百会"(GV20)和 "涌泉"(KI1),每次30分钟,每天1次,每周5天,连续4周。通过莫里斯水迷宫试验观察小鼠的空间学习记忆能力。用 Western 印迹法检测海马中 IL-33 和 ST2 的相对表达。免疫荧光法检测海马CA1区淀粉样β(Aβ)、磷酸化Tau(p-Tau)、IL-33/电离钙结合适配分子1(Iba-1)、ST2/Iba-1、精氨酸酶1(Arg1)/Iba-1和诱导型一氧化氮合酶(iNOS)/Iba-1的阳性表达:结果:与对照组相比,模型组小鼠的逃逸潜伏期延长(PPPPPPPPPPPPP结论:艾灸可以改善小鼠的逃逸潜伏期:艾灸可以改善APP/PS1小鼠的空间学习和记忆能力,减少Aβ和p-Tau的病理沉积,这可能与其上调IL-33/ST2信号通路以调节小胶质细胞向M2方向极化的功能有关。
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Moxibustion influences hippocampal microglia polarization via IL-33/ST2 pathway in Alzheimer's disease mice.

Objectives: To observe the effect of moxibustion on the polarization of microglia towards M2 direction in Alzheimer's disease (AD) mice through the interleukin-33 (IL-33)/growth stimulating gene 2 protein (ST2) signaling pathway.

Methods: Five-month-old APP/PS1 male mice were randomly divided into model and moxibustion (Moxi) groups, and C57BL/6J mice of the same age were as the control group, with 9 mice in each group. In the Moxi group, moxibustion was applied at "Baihui" (GV20) and "Yongquan" (KI1) for 30 min, once a day, 5 days a week for 4 weeks. The spatial learning memory ability was observed by the Morris water maze test. The relative expressions of IL-33 and ST2 in hippocampus were detected by Western blot. The positive expression of amyloid-β (Aβ), phosphorylated Tau (p-Tau), IL-33/ionized calcium binding adapter molecule 1(Iba-1), ST2/Iba-1, arginase 1 (Arg1)/Iba-1 and indu-cible nitric oxide synthase (iNOS)/Iba-1 in hippocampal CA1 region were detected by immunofluorescence.

Results: Compared with the control group, the escape latency of the mice in the model group was prolonged (P<0.001, P<0.01), the number of times to enter the effective area and the percentage of target quadrant swimming time were reduced (P<0.001), the positive expression of both Aβ and p-Tau, the positive expression of iNOS/Iba-1 in the hippocampal CA1 region was increased (P<0.001), while the expression of IL-33 and ST2 protein in hippocampal tissue, the positive expression levels of IL-33/Iba-1, ST2/Iba-1 and Arg1/Iba-1 in hippocampal CA1 region were all decreased (P<0.05, P<0.001). After treatment, compared with the model group, the escape latency of the mice in the moxibustion group was shortened (P<0.001, P<0.01), the number of entries into the effective area and the percentage of target quadrant swimming time were increased (P<0.001), the positive expression of Aβ and p-Tau in the hippocampal CA1 region, and the positive expression of iNOS/Iba-1 were decreased (P<0.001), while the expression of IL-33 and ST2 protein in the hippocampal tissue, the positive expression of IL-33/Iba-1, ST2/Iba-1 and Arg1/Iba-1 in hippocampal CA1 region were all increased (P<0.05, P<0.01, P<0.001).

Conclusions: Moxibustion can improve the spatial learning and memory abilities, reduce the pathological deposition of Aβ and p-Tau in APP/PS1 mice, which may be related to its function in up-regulating the IL-33/ST2 signaling pathway to regulate the polarization of microglia towards M2 direction.

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