Electroacupuncture reduces blood glucose by regulating intestinal flora in type 2 diabetic mice

The development of diabetes is closely related to the gut microbiota in recent studies, which can be influenced by intestinal motility. A few studies report that electroacupuncture (EA) can lower blood glucose. EA can promote colonic motility and influence gut microbes. In this study, we explored the effect of the EA on blood glucose level in mice with type 2 diabetes (T2D) and its mechanism.The T2D mice model, fecal microbiota transplantation mice model, and KitW/Wv mice model （Point mutation of mouse W locus encoding kit gene）were used to investigate the effect of EA on blood glucose as well as the mechanism; The blood glucose and insulin resistance level and the intestinal flora were evaluated. The level of intestinal junction protein, inflammatory cytokines in the serum, interstitial cells of Cajal content, and colonic motility were detected. Lastly, the IKKβ/NF-κB-JNK-IRS-1-AKT pathway was explored.EA lowered the blood glucose level, altered the gut microbiota, and promoted colonic motility in T2D mice. EA-altered microbiota decreased the blood glucose level and insulin resistance in the antibiotics-treated diabetic mice. EA increased tight junction protein, lowered inflammatory factors, and regulated the IKKβ/NF-κB-JNK-IRS-1-AKT pathway in the liver and muscles. EA could not reduce the blood glucose and regulated gut microbiota in the KitW/Wv mice model.EA promoted intestinal motility to regulate the intestinal flora, thereby reducing the level of systemic inflammation, and ultimately lowering the blood glucose by the IKKβ/NF-κB-JNK-IRS-1-AKT signal pathway.背景: 最近的研究表明, 糖尿病的发展与肠道菌群密切相关, 肠道菌群可能会受到肠道运动的影响。一些文献报道电针(EA)可以降低血糖。 EA可以促进结肠运动并影响肠道微生物。在这项研究中, 我们探讨了 EA 对 2 型糖尿病 (T2D) 小鼠血糖水平的影响及其机制。 方法: 采用T2D小鼠模型、FMT(粪菌移植)小鼠模型和KitW/Wv 小鼠模型, 研究电针对血糖的影响及其作用机制, 评估血糖和胰岛素抵抗水平以及肠道菌群。检测肠连接蛋白水平、血清和结肠炎性细胞因子水平、ICC(Cajal间质细胞)含量及结肠运动性。最后, 探索了 IKKβ/NF-κB-JNK-IRS-1-AKT 通路。 结果: 1. EA降低了T2D小鼠的血糖水平, 改变了肠道菌群, 促进了结肠运动。 2. EA 改变的微生物群降低了 ABX(抗生素)治疗的糖尿病小鼠的血糖水平和胰岛素抵抗。 3. EA增加紧密连接蛋白, 降低炎症因子, 并调节肝脏和肌肉中的IKKβ/NF-κB-JNK-IRS-1-AKT通路。 4. EA不能降低KitW/Wv 小鼠模型中的血糖和调节肠道菌群。 结论: 电针通过IKKβ/NF-κBJNK-IRS-1-AKT信号通路促进肠道运动, 调节肠道菌群, 从而降低全身炎症水平, 最终降低血糖。.