Zhan Lianghui, Liu Hao, Zheng Jingru, Meng Jianbiao, Fu Danting, Pang Lisha, Ji Chunlian
Tongde Hospital of Zhejiang Province, Hangzhou, Zhejiang 310014, China.
Zhejiang Academy of Traditional Chinese Medicine, Hangzhou, Zhejiang 310014, China.
Evid Based Complement Alternat Med. 2022 Jun 10;2022:6706622. doi: 10.1155/2022/6706622. eCollection 2022.
Electroacupuncture (EA) at the Zusanli acupoint (ST36) has shown therapeutic potential for sepsis due to its ability to limit inflammation and to regulate gastrointestinal tract symptoms. However, the mechanisms contributing to the effects of EA at ST36 on sepsis and connections with the intestinal flora remain unclear. This study was designed to explore the effects of EA at ST36 on Toll-like receptor 4 signaling and the intestinal flora.
ICR mice were randomly divided into 4 groups: control group, model group, EA group, and sham EA group. EA at ST36 was performed at 2.5 mA and 2 to 100 Hz, and the 30 min of dense wave was achieved over 5 days. A sepsis model was built by intraperitoneal injection of lipopolysaccharide (LPS, 10 mg/mL). The levels of expression of interleukin-1 (IL-1), IL-6, tumor necrosis factor- (TNF-), and IL-10 were detected by enzyme-linked immunosorbent assays, and lactate dehydrogenase (LDH) levels in serum were measured by biochemical tests. Expression levels of Bax, Bcl2, cleaved caspase-3, Toll-like receptor (TLR4), nuclear factor-kappa B (NF-B), and myeloid differentiation factor 88 (MyD88) were assessed by the Western blotting. Terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) staining was used to evaluate apoptosis. The intestinal microecology was assessed via 16S rRNA gene sequencing.
EA at ST36 reduced the expression of IL-1, IL-6, and TNF- and increased the expression of IL-10 to inhibit the inflammatory response. EA at ST36 also inhibited apoptosis, as measured by TUNEL staining, and decreased the Bax/Bcl2 ratio and levels of caspase-3 and cleaved caspase-3, as well as LDH release. Our results suggest that alleviation of sepsis may correlate with the downregulation of levels of TLR4, NF-B, and MyD88. Importantly, EA at ST36 improved the diversity of the intestinal flora and increased the abundance of Firmicutes and Actinobacteria. Conclusion. EA at ST36 prevented sepsis from worsening by inhibiting inflammation and apoptosis, which correlated with the regulation of the TLR4/NF-B/MyD88 signaling axis and modulation of the intestinal flora.
电针足三里穴(ST36)已显示出对脓毒症的治疗潜力,因其能够限制炎症并调节胃肠道症状。然而,电针ST36对脓毒症影响的机制以及与肠道菌群的联系仍不清楚。本研究旨在探讨电针ST36对Toll样受体4信号通路和肠道菌群的影响。
将ICR小鼠随机分为4组:对照组、模型组、电针组和假电针组。电针ST36采用2.5 mA、2至100 Hz,在5天内进行30分钟的密波刺激。通过腹腔注射脂多糖(LPS,10 mg/mL)建立脓毒症模型。采用酶联免疫吸附测定法检测白细胞介素-1(IL-1)、IL-6、肿瘤坏死因子-α(TNF-α)和IL-10的表达水平,通过生化检测测定血清中乳酸脱氢酶(LDH)水平。通过蛋白质免疫印迹法评估Bax、Bcl2、裂解的半胱天冬酶-3、Toll样受体(TLR4)、核因子-κB(NF-κB)和髓样分化因子88(MyD88)的表达水平。采用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)染色评估细胞凋亡。通过16S rRNA基因测序评估肠道微生态。
电针ST36可降低IL-1、IL-6和TNF-α的表达,并增加IL-10的表达以抑制炎症反应。电针ST36还可抑制细胞凋亡,通过TUNEL染色测定,并降低Bax/Bcl2比值以及半胱天冬酶-3和裂解的半胱天冬酶-3水平,以及LDH释放。我们的结果表明,脓毒症的减轻可能与TLR4、NF-κB和MyD88水平的下调有关。重要的是,电针ST36改善了肠道菌群的多样性,并增加了厚壁菌门和放线菌门的丰度。结论:电针ST36通过抑制炎症和细胞凋亡预防脓毒症恶化,这与TLR4/NF-κB/MyD88信号轴的调节和肠道菌群的调节有关。