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Moxibustion influences hippocampal microglia polarization via IL-33/ST2 pathway in Alzheimer's disease mice
Hong-Ying Li1, Yuan Shen2, Lu-Shuang Xie3
1Acupuncture-moxibustion and Tuina College, Chengdu University of Traditional Chinese Medicine, Chengdu 610075, China. 1558494627@qq.com.
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.
Insights
Moxibustion improved spatial memory in Alzheimer's disease (AD) mice by enhancing the interleukin-33 (IL-33)/ST2 pathway, promoting M2 microglia polarization, and reducing amyloid-beta (Aβ) and phosphorylated Tau (p-Tau) pathology.
Area of Science:
- Neuroscience
- Immunology
- Traditional Chinese Medicine
Background:
- Alzheimer's disease (AD) is characterized by neuroinflammation and the accumulation of amyloid-beta (Aβ) and phosphorylated Tau (p-Tau).
- Microglia polarization plays a crucial role in AD pathogenesis, with M2 polarization generally considered neuroprotective.
- The interleukin-33 (IL-33)/ST2 signaling pathway is implicated in regulating microglial polarization.
Purpose of the Study:
- To investigate the effect of moxibustion on M2 microglia polarization in AD mice.
- To explore the role of the IL-33/ST2 signaling pathway in mediating moxibustion's effects on AD.
Main Methods:
- APP/PS1 mice were treated with moxibustion at specific acupoints (GV20, KI1) for 4 weeks.
- Spatial learning and memory were assessed using the Morris water maze test.
- Hippocampal expression of IL-33, ST2, Aβ, p-Tau, and microglial markers (Iba-1) was analyzed via Western blot and immunofluorescence.
Main Results:
- Moxibustion significantly improved spatial learning and memory in AD mice.
- Treatment reduced Aβ and p-Tau deposition and decreased iNOS/Iba-1 expression (M1 microglia marker).
- Moxibustion increased IL-33 and ST2 protein expression, along with IL-33/Iba-1, ST2/Iba-1, and Arg1/Iba-1 (M2 microglia marker) levels.
Conclusions:
- Moxibustion ameliorates cognitive deficits and neuropathology in AD mice.
- The therapeutic effects are associated with the upregulation of the IL-33/ST2 pathway.
- This pathway modulation promotes M2 microglia polarization, suggesting a novel therapeutic strategy for AD.

