Li Chenyang, Qi Xinxin, Xu Lei, Sun Yuan, Chen Yan, Yao Yuhan, Zhao Jun
School of Public Health, Xinjiang Medical University, Urumqi 830011, China.
Xinjiang Key Laboratory for Uighur Medicine, Institute of Materia Medica of Xinjiang, Urumqi 830004, China.
Int J Mol Sci. 2024 Apr 12;25(8):4276. doi: 10.3390/ijms25084276.
This study aimed to investigate the preventive effects of the total polyphenols from (NCTP) on LPS-induced septic acute lung injury (ALI) in mice and its mechanisms. NCTP could significantly ameliorate LPS-induced lung tissue pathological injury in mice as well as lung wet/dry ratio and MPO activities ( < 0.05). NCTP could significantly decrease the blood leukocyte, neutrophil, monocyte, basophil, and eosinophil amounts and LPS contents in ALI mice compared with the model group ( < 0.05), improving lymphocyte amounts ( < 0.05). Moreover, compared with the model group, NCTP could decrease lung tissue TNF-α, IL-6, and IL-1β levels ( < 0.05) and downregulate the protein expression of TLR4, MyD88, TRAF6, IKKβ, IκB-α, p-IκB-α, NF-κB p65, p-NF-κB p65, NLRP3, ASC, and Caspase1 in lung tissues ( < 0.05). Furthermore, NCTP could inhibit ileum histopathological injuries, restoring the ileum tight junctions by increasing the expression of ZO-1 and occludin. Simultaneously, NCTP could reverse the gut microbiota disorder, restore the diversity of gut microbiota, increase the relative abundance of Clostridiales and Lachnospiraceae, and enhance the content of SCFAs (acetic acid, propionic acid, and butyric acid) in feces. These results suggested that NCTP has preventive effects on septic ALI, and its mechanism is related to the regulation of gut microbiota, SCFA metabolism, and the TLR-4/NF-κB and NLRP3 pathways.
本研究旨在探讨[具体来源]总多酚(NCTP)对脂多糖(LPS)诱导的小鼠脓毒症急性肺损伤(ALI)的预防作用及其机制。NCTP可显著改善LPS诱导的小鼠肺组织病理损伤以及肺湿/干比值和髓过氧化物酶(MPO)活性(P<0.05)。与模型组相比,NCTP可显著降低ALI小鼠的血液白细胞、中性粒细胞、单核细胞、嗜碱性粒细胞和嗜酸性粒细胞数量以及LPS含量(P<0.05),并提高淋巴细胞数量(P<0.05)。此外,与模型组相比,NCTP可降低肺组织肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和白细胞介素-1β(IL-1β)水平(P<0.05),并下调肺组织中Toll样受体4(TLR4)、髓样分化因子88(MyD88)、肿瘤坏死因子受体相关因子6(TRAF6)、IκB激酶β(IKKβ)、IκB-α、磷酸化IκB-α(p-IκB-α)、核因子κB p65(NF-κB p65)、磷酸化NF-κB p65(p-NF-κB p65)、NOD样受体蛋白3(NLRP3)、凋亡相关斑点样蛋白(ASC)和半胱天冬酶1(Caspase1)的蛋白表达(P<0.05)。此外,NCTP可抑制回肠组织病理损伤,通过增加紧密连接蛋白1(ZO-1)和闭合蛋白的表达来恢复回肠紧密连接。同时,NCTP可逆转肠道微生物群紊乱,恢复肠道微生物群的多样性,增加梭菌目和毛螺菌科的相对丰度,并提高粪便中短链脂肪酸(乙酸、丙酸和丁酸)的含量。这些结果表明,NCTP对脓毒症ALI具有预防作用,其机制与肠道微生物群、短链脂肪酸代谢以及TLR-4/NF-κB和NLRP3通路的调节有关。