Department of Intensive Care Unit, First Affiliated Hospital of Guizhou University of Chinese Medicine, Guiyang, Guizhou 550001, P.R. China.
Department of Intensive Care Unit, First Affiliated Hospital of Guizhou University of Chinese Medicine, Guiyang, Guizhou 550001, P.R. China.
Mol Med Rep. 2021 Dec;24(6). doi: 10.3892/mmr.2021.12480. Epub 2021 Oct 11.
The aim of the present study was to investigate the therapeutic effects of Tong‑fu‑li‑fei (TFL) decoction on sepsis‑induced injury to the intestinal mucosal barrier and the underlying mechanism. Cecal ligation and puncture (CLP) was used to establish a sepsis model in rats. The post‑surgery death of the rats was recorded to calculate the survival rate. A 4‑kD fluorescein isothiocyanate (FITC)‑dextran assay was used to evaluate the intestinal permeability of the rats. The pathological state of the intestine tissues was detected by hematoxylin and eosin staining and the ultrastructural changes in the endometrium were evaluated by transmission electron microscopy. Enzyme‑linked immunosorbent assay was used to determine the concentrations of interleukin (IL)‑6 and tumor necrosis factor (TNF)‑α in the intestinal tissues and cells. The expression levels of SHP‑2 and PI3K were detected by reverse transcription‑quantitative PCR and western blotting. Sorting by flow cytometry was used to obtain pure dendritic cells (DC), CD8 T cells and natural killer cells. Western blotting was used to evaluate the expression levels of phosphorylated (p)‑AKT and AKT. The results demonstrated that the significantly decreased survival rate caused by CLP surgery was elevated by glutamine (Gln) and TFL treatment. Intestinal permeability was increased by CLP, and greatly suppressed by Gln or TFL treatment. Histopathological changes in the intestinal tissues, such as thinner barrier and atrophied mucosa, and ultrastructure changes such as sharply decreased microvilli and mitochondria dropsy, were observed on sepsis animals; these effects were ameliorated by the introduction of Gln or TFL. The upregulation of SHP‑2, PI3K and p‑AKT induced by CLP was reversed by TFL. The release of IL‑6 and TNF‑α was elevated and the expression of SHP‑2, PI3K and p‑AKT was suppressed in the co‑cultural system of DC cells and CD8 T cells by TFL. Overall, TFL decoction may attenuate immunosuppression to protect intestinal mucosal barrier in sepsis via inhibiting the programmed death1/programmed cell death ligand 1 signal pathway.
本研究旨在探讨通腑利肺汤对脓毒症诱导的肠黏膜屏障损伤的治疗作用及其机制。采用盲肠结扎穿孔术(CLP)建立大鼠脓毒症模型。记录术后大鼠死亡情况,计算生存率。采用 4 kD 荧光素异硫氰酸酯(FITC)-葡聚糖法评估大鼠肠通透性。通过苏木精-伊红(HE)染色检测肠组织病理状态,透射电镜观察肠组织超微结构变化。采用酶联免疫吸附试验(ELISA)法检测肠组织和细胞中白细胞介素(IL)-6和肿瘤坏死因子(TNF)-α的浓度。采用逆转录-定量聚合酶链反应(RT-qPCR)和蛋白质印迹法检测 SHP-2 和 PI3K 的表达水平。采用流式细胞术分选获得纯树突状细胞(DC)、CD8 T 细胞和自然杀伤细胞。蛋白质印迹法检测磷酸化(p)-AKT 和 AKT 的表达水平。结果表明,CLP 手术引起的生存率显著下降,经谷氨酰胺(Gln)和通腑利肺汤(TFL)治疗后升高。CLP 导致肠通透性增加,Gln 或 TFL 治疗可显著抑制其增加。脓毒症动物的肠组织出现明显的组织学变化,如屏障变薄、黏膜萎缩,超微结构变化如微绒毛急剧减少、线粒体水肿等;Gln 或 TFL 治疗可改善这些变化。CLP 诱导的 SHP-2、PI3K 和 p-AKT 上调被 TFL 逆转。TFL 可抑制树突状细胞(DC)和 CD8 T 细胞共培养体系中白细胞介素(IL)-6 和 TNF-α的释放,下调 SHP-2、PI3K 和 p-AKT 的表达。综上所述,通腑利肺汤可能通过抑制程序性死亡 1/程序性死亡配体 1 信号通路,减轻免疫抑制作用,从而保护脓毒症时的肠黏膜屏障。