[电针通过调节NLRP3/半胱天冬酶-1/ Gasdermin D信号通路改善溃疡性结肠炎小鼠结肠黏膜屏障损伤并抑制细胞焦亡]

[Electroacupuncture improves colonic mucosal barrier damage by regulating NLRP3/Caspase-1/GSDMD signaling pathway and inhibiting pyroptosis in ulcerative colitis mice].

作者信息

Wang Xi-Han, Liu Ji-Dong, Qu Yi, Dong Jia-Zi, Wang Jian-Bo, Xue Ya-Nan, Li Yang, Zhang Jia-Hao, Jin Lu, Wang Tian-Lang, Wang Xi-Ning

机构信息

College of Acupuncture and Tuina, Shenyang 110847, China.

Key Laboratory of Chinese Ministry of Education for Chinese Medical Viscera-State Theory and Applications, Liaoning University of Traditional Chinese Medicine, Shenyang 110847.

出版信息

Zhen Ci Yan Jiu. 2025 Mar 25;50(3):277-286. doi: 10.13702/j.1000-0607.20240402.

Abstract

OBJECTIVES

To observe the effect of electroacupuncture (EA) at "Tianshu" (ST25) and "Zusanli" (ST36) on NOD-like receptor protein 3(NLRP3)/cysteine aspartate specific protease 1 (Caspase-1)/gasdermin D (GSDMD) pyroptosis signaling pathway in ulcerative colitis (UC) mice, so as to explore its mechanism in improving UC by protecting intestinal barrier.

METHODS

Fifty male C57BL/6 mice were randomly divided into normal, model, EA, sham acupuncture and medication groups, with 10 mice in each group. The UC mouse model was established by 3% DSS solution free drinking for 7 consecutive days. The mice in the EA group received EA (2 Hz/10 Hz, 0.2 mA) at bilateral ST25 and ST36 for 20 min, while the mice in the sham acupuncture group received only sham acupuncture (light and shallow acupunture at ST25 and ST36). Mice in the medication group were orally administered mesalazine (33.4 g/kg) solution. All the interventions were performed once daily for a total of 7 days. The changes of body weight, stool shape and hematochezia of mice, the disease activity index (DAI) score, and the length of colon were recorded. The intestinal mucosal permeability was observed by small animal imaging system. HE staining was used to observe the pathological changes of colon tissue. TUNEL staining was used to observe the apoptosis of colon cells. The contents of interleukin (IL)-18 and IL-1β in serum were detected by ELISA. The average fluorescence intensity of tumor necrosis factor-α (TNF-α) and IL-6 in colon tissue was detected by immunofluorescence. The positive expression of IL-18 and IL-1β in colon tissue was detected by immunohistochemistry. The relative expression levels of zonula occludens-1 (ZO-1), Occludin, NLRP3, Caspase-1 and GSDMD in colon tissue were detected by Western blot. The mRNA expressions of NLRP3, Caspase-1 and GSDMD in colon tissue were detected by qPCR.

RESULTS

After modeling, the DAI, inflammatory infiltration, number of apoptotic cells, fluorescence intensity of TNF-α, IL-6 and FITC, positive expression rate of IL-18 and IL-1β, mRNA and protein expression levels of NLRP3, Caspase-1 and GSDMD, serum IL-18 and IL-1β contents were significantly increased (<0.01) in the model group relevant to the normal group. At the same time, the colon length, ZO-1 and Occludin protein expression were significantly reduced (<0.01). The increased DAI, inflammatory infiltration, number of apoptotic cells, fluorescence intensity of TNF-α, IL-6 and FITC, positive rate of IL-18 and IL-1β, mRNA and protein expression levels of NLRP3, Caspase-1 and GSDMD, serum IL-18 and IL-1β contents, and the decreased colon length, ZO-1 and Occludin protein expression were all reversed after the EA and medication interventions compared with the model group and in the EA group than in the sham acupuncture group (<0.01, <0.05).

CONCLUSIONS

EA can protect the intestinal mucosal permeability in UC mice, which may be related to its functions in regulating the NLRP3/Caspase-1/GSDMD axis and inhibiting pyroptosis, thereby alleviating the inflammatory injury of intestinal mucosa.

摘要

目的

观察电针“天枢”(ST25)和“足三里”(ST36)对溃疡性结肠炎(UC)小鼠NOD样受体蛋白3(NLRP3)/半胱天冬酶-1(Caspase-1)/gasdermin D(GSDMD)焦亡信号通路的影响,以探讨其通过保护肠屏障改善UC的机制。

方法

将50只雄性C57BL/6小鼠随机分为正常组、模型组、电针组、假针刺组和药物组,每组10只。采用3% DSS溶液自由饮用连续7天建立UC小鼠模型。电针组小鼠于双侧ST25和ST36接受电针治疗(2 Hz/10 Hz,0.2 mA)20分钟,假针刺组小鼠仅接受假针刺(在ST25和ST36轻度浅刺)。药物组小鼠口服美沙拉嗪(33.4 g/kg)溶液。所有干预均每日进行1次,共7天。记录小鼠体重、粪便形状和便血情况、疾病活动指数(DAI)评分及结肠长度。采用小动物成像系统观察肠黏膜通透性。苏木精-伊红(HE)染色观察结肠组织病理变化。TUNEL染色观察结肠细胞凋亡情况。采用酶联免疫吸附测定(ELISA)法检测血清白细胞介素(IL)-18和IL-1β含量。采用免疫荧光法检测结肠组织中肿瘤坏死因子-α(TNF-α)和IL-6的平均荧光强度。采用免疫组织化学法检测结肠组织中IL-18和IL-1β的阳性表达。采用蛋白质免疫印迹法检测结肠组织中紧密连接蛋白-1(ZO-1)、闭合蛋白、NLRP3、Caspase-1和GSDMD的相对表达水平。采用实时荧光定量聚合酶链反应(qPCR)法检测结肠组织中NLRP3、Caspase-1和GSDMD的mRNA表达。

结果

造模后,模型组与正常组相比,DAI、炎症浸润、凋亡细胞数、TNF-α、IL-6和异硫氰酸荧光素(FITC)荧光强度、IL-18和IL-1β阳性表达率、NLRP3、Caspase-1和GSDMD的mRNA和蛋白表达水平、血清IL-18和IL-1β含量均显著升高(<0.01)。同时,结肠长度、ZO-1和闭合蛋白蛋白表达显著降低(<0.01)。与模型组相比,电针和药物干预后,DAI升高、炎症浸润、凋亡细胞数、TNF-α、IL-6和FITC荧光强度、IL-18和IL-1β阳性率、NLRP3、Caspase-1和GSDMD的mRNA和蛋白表达水平、血清IL-18和IL-1β含量升高以及结肠长度、ZO-1和闭合蛋白蛋白表达降低的情况均得到逆转,且电针组与假针刺组相比差异有统计学意义(<0.01,<0.05)。

结论

电针可保护UC小鼠的肠黏膜通透性,这可能与其调节NLRP3/Caspase-1/GSDMD轴及抑制焦亡的作用有关,从而减轻肠黏膜的炎症损伤。

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