[电针通过调节NLRP3/Caspase-1/GSDMD信号通路,抑制溃疡性结肠炎小鼠焦亡,改善结肠黏膜屏障损伤]。

Q3 Medicine
Xi-Han Wang, Ji-Dong Liu, Yi Qu, Jia-Zi Dong, Jian-Bo Wang, Ya-Nan Xue, Yang Li, Jia-Hao Zhang, Lu Jin, Tian-Lang Wang, Xi-Ning Wang
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引用次数: 0

摘要

目的:观察电针“天术”(ST25)和“足三里”(ST36)对溃疡性结肠炎(UC)小鼠nod样受体蛋白3(NLRP3)/半胱氨酸天冬氨酸特异性蛋白酶1 (Caspase-1)/气皮蛋白D (GSDMD)焦亡信号通路的影响,探讨其通过保护肠道屏障改善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、EA组、假针刺组和给药组,每组10只。采用3% DSS溶液连续无饮7 d建立UC小鼠模型。EA组小鼠在双侧ST25和ST36处进行2 Hz/10 Hz, 0.2 mA的电刺激,持续20 min,而假针组小鼠仅在ST25和ST36处进行轻、浅针刺。给药组小鼠口服美沙拉嗪溶液(33.4 g/kg)。所有干预措施每天进行一次,共7天。记录小鼠体重、粪便形态、便血、疾病活动指数(DAI)评分、结肠长度的变化。采用活体小动物显像系统观察肠粘膜通透性。采用HE染色观察大鼠结肠组织病理变化。TUNEL染色观察结肠细胞凋亡情况。采用ELISA法检测血清白细胞介素(IL)-18、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。免疫组化法检测结肠组织中IL-18、IL-1β的阳性表达。Western blot检测结肠组织中zonula occludens-1 (ZO-1)、Occludin、NLRP3、Caspase-1、GSDMD的相对表达量。采用qPCR检测结肠组织中NLRP3、Caspase-1、GSDMD mRNA的表达。结果:造模后,大鼠DAI、炎性浸润、凋亡细胞数、TNF-α、IL-6、FITC荧光强度、IL-18、IL-1β阳性表达率、NLRP3、Caspase-1、GSDMD mRNA及蛋白表达水平、血清IL-18、IL-1β含量均显著升高(ppppp)。EA具有保护UC小鼠肠黏膜通透性的作用,这可能与其调节NLRP3/Caspase-1/GSDMD轴,抑制焦亡的功能有关,从而减轻肠黏膜的炎症损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Electroacupuncture improves colonic mucosal barrier damage by regulating NLRP3/Caspase-1/GSDMD signaling pathway and inhibiting pyroptosis in ulcerative colitis mice].

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 in vivo 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 (P<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 (P<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 (P<0.01, P<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.

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来源期刊
针刺研究
针刺研究 Medicine-Medicine (all)
CiteScore
1.30
自引率
0.00%
发文量
0
期刊介绍: Acupuncture Research was founded in 1976. It is an acupuncture academic journal supervised by the State Administration of Traditional Chinese Medicine, co-sponsored by the Institute of Acupuncture of the China Academy of Chinese Medical Sciences and the Chinese Acupuncture Association. This journal is characterized by "basic experimental research as the main focus, taking into account clinical research and reporting". It is the only journal in my country that focuses on reporting the mechanism of action of acupuncture. The journal has been changed to a monthly journal since 2018, published on the 25th of each month, and printed in full color. The manuscript acceptance rate is about 10%, and provincial and above funded projects account for about 80% of the total published papers, reflecting the latest scientific research results in the acupuncture field and has a high academic level. Main columns: mechanism discussion, clinical research, acupuncture anesthesia, meridians and acupoints, theoretical discussion, ideas and methods, literature research, etc.
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