Walnut Protein Peptides Ameliorate DSS-Induced Ulcerative Colitis Damage in Mice: An in Silico Analysis and in Vivo Investigation

被引:17
作者
Hong, Zishan [1 ,2 ]
Shi, Chongying [1 ,2 ]
Hu, Xia [2 ,3 ]
Chen, Jinlian [2 ]
Li, Tingting [2 ]
Zhang, Li [2 ]
Bai, Yuying [2 ]
Dai, Jingjing [4 ]
Sheng, Jun [2 ]
Xie, Jing [1 ,2 ]
Tian, Yang [1 ,2 ,4 ]
机构
[1] Yunnan Agr Univ, Coll Food Sci & Technol, Engn Res Ctr Dev & Utilizat Food & Drug Homologou, Minist Educ, Kunming 650201, Yunnan, Peoples R China
[2] Yunnan Agr Univ, Yunnan Prov Key Lab Precis Nutr & Personalized Fo, Kunming 650201, Yunnan, Peoples R China
[3] Yunnan Agr Univ, Coll Food Sci & Technol, Kunming 650201, Yunnan, Peoples R China
[4] Puer Univ, Sch Tea & Coffee, Puer 665000, Peoples R China
关键词
walnut protein peptides; network pharmacology; ulcerative colitis; TLR4-MAPK signaling pathway; gut microbiota; INHIBITORY PEPTIDES; MICROBIOTA; MECHANISMS; INDUCTION; BARRIER; STRESS; TLR4;
D O I
10.1021/acs.jafc.3c04220
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Walnut (Juglans regia L.) is a food with food-medicine homology, whose derived protein peptides have been shown to have anti-inflammatory activity in vitro. However, the effects and mechanisms of walnut protein peptides on ulcerative colitis (UC) in vivo have not been systematically and thoroughly investigated. In this study, we applied virtual screening and network pharmacology screening of bioactive peptides to obtain three novel WPPs (SHTLP, HYNLN, and LGTYP) that may alleviate UC through TLR4-MAPK signaling. In vivo studies have shown that WPPs improve intestinal mucosal barrier dysfunction and reduce inflammation by inhibiting activation of the TLR4-MAPK pathway. In addition, WPPs restore intestinal microbial homeostasis by reducing harmful bacteria (Helicobacter and Bacteroides) and increasing the relative abundance of beneficial bacteria (Candidatus_Saccharimonas). Our study showed that the WPPs obtained by virtual screening were effective in ameliorating colitis, which has important implications for future screening of bioactive peptides from medicinal food homologues as drugs or dietary supplements.
引用
收藏
页码:15604 / 15619
页数:16
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