Department of Gastroenterology, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Cancer Research Laboratory, Binzhou Medical University Hospital, Binzhou, Shandong, China.
Neuromodulation. 2024 Feb;27(2):302-311. doi: 10.1016/j.neurom.2023.01.005. Epub 2023 Feb 3.
Inflammatory bowel disease (IBD) is characterized by chronic progressive intestinal inflammation. Sacral nerve stimulation (SNS) ameliorates colon inflammation caused by IBD. The aim of this study was to investigate the antiinflammatory benefits of SNS in colitis rats and explore the roles of the cholinergic antiinflammatory pathway, macrophage autophagy, and nucleotide oligomerization domain-like receptor thermal protein domain associated protein 3 (NLRP3) inflammatory bodies.
Rats were divided into four groups: healthy control, dextran sulfate sodium (DSS), DSS + sham-SNS, and DSS + SNS groups. An electrode was surgically placed in the right sacral nerve (S3) for stimulation. The disease activity index (DAI) score was recorded each day, and the degree of inflammatory injury was evaluated using hematoxylin and eosin staining. The alpha7 nicotinic acetylcholine receptor (α7nAChR) and autophagy- and NLRP3-related factors were assessed using immunofluorescence staining and Western blotting.
The DSS group showed a higher DAI score, colon shortening, upregulated proinflammatory action, and colon damage, and the DSS + SNS group showed significantly improved symptoms. The number of α7nAChR+ cells and the expression level of autophagy decreased in the DSS group but increased in the DSS + SNS group. Conversely, the DSS group showed increased activation of NLRP3 inflammatory bodies, whereas the DSS + SNS group showed decreased activation of NLRP3 inflammatory bodies.
In this study, SNS ameliorated colon inflammation by enhancing macrophage autophagy and inhibiting the activation of NLRP3 inflammatory bodies, which may be related to the opening of the cholinergic antiinflammatory pathway.
炎症性肠病(IBD)的特征是慢性进行性肠道炎症。骶神经刺激(SNS)可改善 IBD 引起的结肠炎症。本研究旨在探讨 SNS 对结肠炎大鼠的抗炎作用,并探讨胆碱能抗炎途径、巨噬细胞自噬和核苷酸寡聚化结构域样受体热蛋白结构域相关蛋白 3(NLRP3)炎症小体的作用。
大鼠分为四组:健康对照组、葡聚糖硫酸钠(DSS)组、DSS+假刺激 SNS 组和 DSS+SNS 组。手术将电极放置在右侧骶神经(S3)处以进行刺激。每天记录疾病活动指数(DAI)评分,并通过苏木精和伊红染色评估炎症损伤程度。使用免疫荧光染色和 Western blot 评估α7 烟碱型乙酰胆碱受体(α7nAChR)和自噬及 NLRP3 相关因子。
DSS 组的 DAI 评分、结肠缩短、促炎作用增强和结肠损伤加重,DSS+SNS 组的症状明显改善。DSS 组的α7nAChR+细胞数量和自噬表达水平降低,而 DSS+SNS 组则增加。相反,DSS 组的 NLRP3 炎症小体激活增加,而 DSS+SNS 组的 NLRP3 炎症小体激活减少。
在本研究中,SNS 通过增强巨噬细胞自噬和抑制 NLRP3 炎症小体的激活来改善结肠炎症,这可能与胆碱能抗炎途径的开放有关。