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无锡市第二中医医院针灸科,江苏无锡 214121
安徽中医药大学第二附属医院康复二科,合肥 230061
安徽中医药大学第一附属医院针灸康复科
无锡市第二人民医院针灸科
✉李飞,主任医师。E-mail:316029622@qq.com
收稿:2024-11-25,
网络首发:2025-07-04,
纸质出版:2025-11-12
移动端阅览
邱帅辉, 杨琪琪, 杨骏, 等. 基于NLRP3/Caspase-1/GSDMD信号通路探讨化瘀通络灸对血管性痴呆大鼠学习记忆能力及海马CA1区神经损伤的影响[J]. 中国针灸, 2025,45(11):1591-1599.
QIU Shuaihui, YANG Qiqi, YANG Jun, et al. Effects of
邱帅辉, 杨琪琪, 杨骏, 等. 基于NLRP3/Caspase-1/GSDMD信号通路探讨化瘀通络灸对血管性痴呆大鼠学习记忆能力及海马CA1区神经损伤的影响[J]. 中国针灸, 2025,45(11):1591-1599. DOI: 10.13703/j.0255-2930.20241125-0001.
QIU Shuaihui, YANG Qiqi, YANG Jun, et al. Effects of
目的:
2
观察化瘀通络灸对血管性痴呆(VD)大鼠NOD样受体热蛋白结构域相关蛋白3(NLRP3)/半胱氨酸天冬氨酸蛋白酶-1(Caspase-1)/消皮素D(GSDMD)信号通路的影响,探讨化瘀通络灸对学习记忆能力及海马CA1区神经损伤改善的机制。
方法:
2
80只SPF级雄性Wistar大鼠,通过水迷宫实验剔除3只,从剩余大鼠中随机选取12只作为假手术组,剩余大鼠采用改良双侧颈总动脉结扎法制备VD模型,将造模成功的36只大鼠随机分为模型组、西药组和艾灸组,每组12只。西药组予尼莫地平溶液(12 mg/kg)灌胃干预;艾灸组予以化瘀通络灸干预,予“神庭”“大椎”悬灸,予“百会”隔附子饼灸,每穴每次灸20 min。均每日1次,连续干预21 d。造模前后及干预后,采用Morris水迷宫实验评估大鼠认知功能。干预后,采用免疫荧光法观察大鼠海马CA1区小胶质细胞活化及形态,透射电镜观察大鼠海马CA1区神经元超微结构,Western blot法检测大鼠海马CA1区NLRP3、凋亡相关斑点样蛋白(ASC)、Caspase-1、GSDMD及白细胞介素-1β(IL-1β)蛋白表达,ELISA法检测大鼠海马CA1区白细胞介素-6(IL-6)、白细胞介素-8(IL-8)及肿瘤坏死因子-α(TNF-α)含量。
结果:
2
与假手术组比较,模型组大鼠平均逃避潜伏期延长(
P
<
0.01),穿越平台次数减少(
P
<
0.01);海马CA1区小胶质细胞突起增厚,胞质肥大,离子钙结合衔接分子1(IBA-1)相对荧光强度增强(
P
<
0.05);海马CA1区神经元超微结构严重损害,粗面内质网肿胀,线粒体畸形、肿胀,甚至部分线粒体嵴断裂溶解,呈空泡样变化;海马CA1区NLRP3、ASC、Caspase-1、GSDMD、IL-1β蛋白表达升高(
P
<
0.001),IL-6、IL-8及TNF-α含量增加(
P
<
0.001)。与模型组比较,西药组与艾灸组大鼠平均逃避潜伏期缩短(
P
<
0.01),穿越平台次数增加(
P
<
0.01);海马CA1区小胶质细胞突起较细小,IBA-1相对荧光强度降低(
P
<
0.05);海马CA1区神经元超微结构损伤均有不同程度改善;海马CA1区NLRP3、ASC、Caspase-1、GSDMD、IL-1β蛋白表达降低(
P
<
0.001),IL-6、IL-8及TNF-α含量降低(
P
<
0.001)。与西药组比较,艾灸组大鼠平均逃避潜伏期缩短(
P
<
0.05),穿越平台次数增加(
P
<
0.05);海马CA1区IBA-1相对荧光强度降低(
P
<
0.05);海马CA1区神经元超微结构损伤改善;海马CA1区NLRP3、ASC、Caspase-1、GSDMD、IL-1β蛋白表达降低(
P
<
0.001),IL-6、IL-8及TNF-α含量降低(
P
<
0.001)。
结论:
2
化瘀通络灸能提高VD大鼠学习记忆能力,抑制小胶质细胞过度活化,改善海马CA1区神经损伤,其机制可能与调控NLRP3/Caspase-1/GSDMD信号通路,减轻炎症反应有关。
Objective
2
To observe the effect of
Huayu Tongluo
moxibustion on the NOD-like receptor protein 3 (NLRP3)/cysteine-aspartic acid protease-1 (Caspase-1)/gasdermin D (GSDMD) signaling pathway in rats with vascular dementia (VD)
and to explore its mechanism in improving learning and memory ability and alleviating neuronal injury in the hippocampal CA1 region.
Methods
2
A total of 80 SPF-grade male Wistar rats were included. Three rats were excluded based on the Morris water maze test. From the remaining rats
12 were randomly selected as the sham operation group. The rest were used to establish VD models via modified bilateral common carotid artery ligation. Thirty-six successfully modeled rats were randomly divided into a model group
a medication group
and a moxibustion group
with 12 rats in each group. The medication group was treated with nimodipine solution (12 mg/kg) via gavage. The moxibustion group was treated with
Huayu Tongluo
moxibustion. The suspended moxibustion was applied at Shenting (GV24) and Dazhui (GV14)
and aconite cake-separated moxibustion was applied at Baihui (GV20)
with each acupoint treated for 20 min. All treatments were administered once daily for 21 consecutive days. Before and after modeling
and after intervention
the Morris water maze test was used to assess cognitive function. After intervention
the activation and morphology of microglia in the hippocampal CA1 region were observed by immunofluorescence. Ultrastructure of hippocampal CA1 neurons was examined by transmission electron microscopy. Western blot was used to detect protein expression of NLRP3
apoptosis-associated speck-like protein (ASC)
Caspase-1
GSDMD
and interleukin-1β (IL-1β) in the hippocampal CA1 region. ELISA was used to detect the content of IL-6
IL-8
and tumor necrosis factor-α (TNF-α) in the hippocampal CA1 region.
Results
2
Compared with the sham ope
ration group
the model group showed longer mean escape latency (
P
<
0.01) and fewer platform crossings (
P
<
0.01); the microglial processes in the hippocampal CA1 region were thickened
cytoplasm was hypertrophic
and relative fluorescence intensity of ionized calcium-binding adapter molecule 1 (IBA-1) was increased (
P
<
0.05); the neuronal ultrastructure in the CA1 region was severely damaged
rough endoplasmic reticulum was swollen
mitochondria were deformed and swollen
some cristae were ruptured or dissolved
showing vacuolar changes; the protein expression of NLRP3
ASC
Caspase-1
GSDMD
and IL-1β
as well as levels of IL-6
IL-8
and TNF-α were significantly elevated (
P
<
0.001). Compared with the model group
both the medication group and the moxibustion group showed shortened mean escape latency (
P
<
0.01) and increased platform crossings (
P
<
0.01); the microglial processes were thinner
and IBA-1 fluorescence intensity was decreased (
P
<
0.05); the neuronal ultrastructure in the CA1 region was partially improved; the protein expression of NLRP3
ASC
Caspase-1
GSDMD
and IL-1β
and levels of IL-6
IL-8
and TNF-α were significantly reduced (
P
<
0.001). Compared with the medication group
the moxibustion group showed shortened mean escape latency (
P
<
0.05) and more platform crossings (
P
<
0.05); the IBA-1 fluorescence intensity was decreased (
P
<
0.05); the neuronal ultrastructure in the CA1 region was improved; the protein expression of NLRP3
ASC
Caspase-1
GSDMD
and IL-1β
as well as levels of IL-6
IL-8
and TNF-α
were significantly lower (
P
<
0.001).
Conclusion
2
The
Huayu Tongluo
moxibustion could enhance learning and memory abilities in VD rats
inhibit excessive activation of microglia
and alleviate neuronal injury in the hippocam
pal CA1 region. Its mechanism may involve modulation of the NLRP3/Caspase-1/GSDMD signaling pathway
reduction of inflammatory responses.
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