Xingcai Gao, Bing Zheng, Qing Zhou, Jun Li, Jianhua Xie, Yi Chen, Xiaole Zhao, Xiaobo Hu and Qiang Yu*,
{"title":"黄精多糖靶向肠道微生物抑制nod2驱动的炎症和调节结肠炎胆汁酸代谢。","authors":"Xingcai Gao, Bing Zheng, Qing Zhou, Jun Li, Jianhua Xie, Yi Chen, Xiaole Zhao, Xiaobo Hu and Qiang Yu*, ","doi":"10.1021/acs.jafc.5c04155","DOIUrl":null,"url":null,"abstract":"<p ><i>Polygonatum cyrtonema</i>, a traditional medicinally edible herb, exhibits potent anti-inflammatory activity. Its primary active components are fermentable polysaccharides, which enhance the proliferation of beneficial gut microbiota. However, the role of the gut microbiota in the anti-inflammatory effects of <i>P. cyrtonema</i> polysaccharides (PCPs) has not been adequately explored, and the mechanisms involved remain largely unelucidated. Our results demonstrated that PCP significantly alleviated DSS-induced colitis symptoms and enhanced beneficial gut microbiota abundance and diversity. Notably, gut microbiota modulated by PCP exhibited a similar capacity to mitigate colitis symptoms. Further mechanistic studies revealed that both PCP and the PCP-modulated gut microbiota improved colitis by inhibiting the overactivation of the NOD2-mediated autophagy-inflammation pathway and reducing the synthesis of the bile acid metabolite LTC4. Importantly, LTC4 levels were positively correlated to the NOD2-autophagy-inflammation pathway. Collectively, our findings identified PCP as a novel prebiotic preserving gut health through microbiota-mediated homeostasis regulation, offering new therapeutic strategies for inflammatory disorders.</p>","PeriodicalId":41,"journal":{"name":"Journal of Agricultural and Food Chemistry","volume":"73 32","pages":"20190–20204"},"PeriodicalIF":6.2000,"publicationDate":"2025-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Polygonatum cyrtonema Polysaccharides Target Gut Microbiota to Suppress NOD2-Driven Inflammation and Modulate Bile Acid Metabolism in Colitis\",\"authors\":\"Xingcai Gao, Bing Zheng, Qing Zhou, Jun Li, Jianhua Xie, Yi Chen, Xiaole Zhao, Xiaobo Hu and Qiang Yu*, \",\"doi\":\"10.1021/acs.jafc.5c04155\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p ><i>Polygonatum cyrtonema</i>, a traditional medicinally edible herb, exhibits potent anti-inflammatory activity. Its primary active components are fermentable polysaccharides, which enhance the proliferation of beneficial gut microbiota. However, the role of the gut microbiota in the anti-inflammatory effects of <i>P. cyrtonema</i> polysaccharides (PCPs) has not been adequately explored, and the mechanisms involved remain largely unelucidated. Our results demonstrated that PCP significantly alleviated DSS-induced colitis symptoms and enhanced beneficial gut microbiota abundance and diversity. Notably, gut microbiota modulated by PCP exhibited a similar capacity to mitigate colitis symptoms. Further mechanistic studies revealed that both PCP and the PCP-modulated gut microbiota improved colitis by inhibiting the overactivation of the NOD2-mediated autophagy-inflammation pathway and reducing the synthesis of the bile acid metabolite LTC4. Importantly, LTC4 levels were positively correlated to the NOD2-autophagy-inflammation pathway. Collectively, our findings identified PCP as a novel prebiotic preserving gut health through microbiota-mediated homeostasis regulation, offering new therapeutic strategies for inflammatory disorders.</p>\",\"PeriodicalId\":41,\"journal\":{\"name\":\"Journal of Agricultural and Food Chemistry\",\"volume\":\"73 32\",\"pages\":\"20190–20204\"},\"PeriodicalIF\":6.2000,\"publicationDate\":\"2025-07-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Agricultural and Food Chemistry\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jafc.5c04155\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"AGRICULTURE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Agricultural and Food Chemistry","FirstCategoryId":"97","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jafc.5c04155","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, MULTIDISCIPLINARY","Score":null,"Total":0}
Polygonatum cyrtonema Polysaccharides Target Gut Microbiota to Suppress NOD2-Driven Inflammation and Modulate Bile Acid Metabolism in Colitis
Polygonatum cyrtonema, a traditional medicinally edible herb, exhibits potent anti-inflammatory activity. Its primary active components are fermentable polysaccharides, which enhance the proliferation of beneficial gut microbiota. However, the role of the gut microbiota in the anti-inflammatory effects of P. cyrtonema polysaccharides (PCPs) has not been adequately explored, and the mechanisms involved remain largely unelucidated. Our results demonstrated that PCP significantly alleviated DSS-induced colitis symptoms and enhanced beneficial gut microbiota abundance and diversity. Notably, gut microbiota modulated by PCP exhibited a similar capacity to mitigate colitis symptoms. Further mechanistic studies revealed that both PCP and the PCP-modulated gut microbiota improved colitis by inhibiting the overactivation of the NOD2-mediated autophagy-inflammation pathway and reducing the synthesis of the bile acid metabolite LTC4. Importantly, LTC4 levels were positively correlated to the NOD2-autophagy-inflammation pathway. Collectively, our findings identified PCP as a novel prebiotic preserving gut health through microbiota-mediated homeostasis regulation, offering new therapeutic strategies for inflammatory disorders.
期刊介绍:
The Journal of Agricultural and Food Chemistry publishes high-quality, cutting edge original research representing complete studies and research advances dealing with the chemistry and biochemistry of agriculture and food. The Journal also encourages papers with chemistry and/or biochemistry as a major component combined with biological/sensory/nutritional/toxicological evaluation related to agriculture and/or food.