Department of Gastroenterology, Affiliated Hospital of Jiangnan University, Wuxi 214122, China.
School of Medicine, Jiangnan University, Wuxi 214122, China.
Nutrients. 2023 Feb 1;15(3):739. doi: 10.3390/nu15030739.
Ulcerative colitis (UC), one of the typical inflammatory bowel diseases caused by dysregulated immunity, still requires novel therapeutic medicine with high efficacy and low toxicity. has been widely used to treat different health problems especially gastrointestinal sickness in China for thousands of years. Here, we isolated, purified, and characterized a novel low weight polysaccharide (HEP10, Mw: 9.9 kDa) from the mycelia of in submerged culture. We explored the therapeutic effect of HEP10 on UC and explored its underlying mechanisms. On one hand, HEP10 suppressed the production of TNF-α, IL-1β, IL-6, inducible iNOS, and COX-2 in LPS challenged murine macrophage RAW264.7 cells, as well as in colons from DSS-induced colitis mice. On the other hand, HEP10 treatment markedly suppressed the activation of NLRP3 inflammasome, NF-κB, AKT, and MAPK pathways. Moreover, HEP10 reversed DSS-induced alternation of the gut community composition and structure by significantly increasing and also promoting functional shifts in gut microbiota. Structural equation modeling also highlighted that HEP10 can change widely through gut microbiota. In conclusion, HEP10 has a better prebiotic effect than the crude polysaccharides of , which can be used as a novel dietary supplement and prebiotic to ameliorate colitis.
溃疡性结肠炎(UC)是一种由免疫失调引起的典型炎症性肠病,仍需要具有高效低毒的新型治疗药物。在中国, 已被广泛用于治疗各种健康问题,尤其是胃肠道疾病,已有数千年的历史。在这里,我们从 的菌丝体中分离、纯化并表征了一种新型低分子量多糖(HEP10,Mw:9.9 kDa)。我们探索了 HEP10 对 UC 的治疗作用及其潜在机制。一方面,HEP10 抑制了 LPS 刺激的巨噬细胞 RAW264.7 细胞和 DSS 诱导的结肠炎小鼠结肠中 TNF-α、IL-1β、IL-6、诱导型 iNOS 和 COX-2 的产生。另一方面,HEP10 治疗显著抑制 NLRP3 炎性小体、NF-κB、AKT 和 MAPK 途径的激活。此外,HEP10 通过显著增加 和促进肠道微生物群的功能转变,逆转了 DSS 诱导的肠道群落组成和结构的改变。结构方程模型也强调了 HEP10 可以通过肠道微生物群发生广泛变化。总之,HEP10 比 的粗多糖具有更好的益生元作用,可作为新型膳食补充剂和益生元用于改善结肠炎。