Abstract

Sepsis results in high morbidity and mortality. Immunomodulation strategies could be an adjunctive therapy to treat sepsis. Acupuncture has also been used widely for many years in China to treat sepsis. However, the underlying mechanisms are not well-defined. We demonstrated here that EA preconditioning at ST36 obviously ameliorated CLP-induced intestinal injury and high permeability and reduced the mortality of CLP-induced sepsis rats. Moreover, electroacupuncture (EA) pretreatment exerted protective effects on intestinal mucosal immune barrier by increasing the concentration of sIgA and the percentage of CD3+, γ/δ, and CD4+ T cells and the ratio of CD4+/CD8+ T cells. Although EA at ST36 treatments immediately after closing the abdomen in the CLP procedure with low-frequency or high-frequency could not reduce the mortality of CLP-induced sepsis in rats, these EA treatments could also significantly improve intestinal injury index in rats with sepsis and obviously protected intestinal mucosal immune barrier. In conclusion, our findings demonstrated that EA at ST36 could improve intestinal mucosal immune barrier in sepsis induced by CLP, while the precise mechanism underlying the effects needs to be further elucidated.

Highlights

  • Sepsis frequently occurs after trauma, burns, hemorrhage, or abdominal surgery

  • The object of this study, based on the rat model of sepsis induced by CLP, was to observe the effects of EA at ST36 on the intestinal mucosal immune barrier

  • EA preconditioning significantly increased the percentage of CD3+, γ/δ, and CD4+ T cells and the ratio of

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Summary

Introduction

Sepsis frequently occurs after trauma, burns, hemorrhage, or abdominal surgery. It can progress to multiorgan failure (MOF). Sepsis is a complex immune syndrome characterized by an imbalance between pro- and anti-inflammatory mediators systemically released in high amounts (cytokine storm) in response to an infection, while the precise pathophysiologic mechanisms underlying the development of multiorgan failure (MOF) remain elusive [5, 6]. The gut is often described as the motor of MOF because the loss of its integrity is a critical comorbidity factor for patients after HS, as well as trauma, surgery, sepsis, and burn injuries [7, 8]. The intestinal mucosal immune system has recently emerged as a potential target in sepsis treatment. The object of this study, based on the rat model of sepsis induced by CLP, was to observe the effects of EA at ST36 on the intestinal mucosal immune barrier

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