Hamad Rafique , Rui Dong , Liu Tianqi , Zhen Ma , Xinzhong Hu , Muhammad Zubair Khalid , Waseem Khalid
{"title":"Oat peptide ameliorates cognitive impairment via mediating gut-brain axis in mice: A multi-omics approach","authors":"Hamad Rafique , Rui Dong , Liu Tianqi , Zhen Ma , Xinzhong Hu , Muhammad Zubair Khalid , Waseem Khalid","doi":"10.1016/j.jafr.2025.102394","DOIUrl":null,"url":null,"abstract":"<div><div>Oat protein-derived bioactive peptide (RW-9) has been reported to exert beneficial effects in memory deficits. However, the mechanisms underline the neuroprotective effects of RW-9 peptide against Alzheimer disease (AD) like symptoms remain unclear. In this study, we found that RW-9 intervention showed various improving effects in cognitive-behavioral tests and alleviated the oxidative stress and inflammation in scopolamine-induced mice model. The H&E staining results demonstrated the protective effects of RW-9 on hippocampal neurons. Proteomic analysis of hippocampus revealed the upregulation of memory related proteins, including Grin3a, Ppp2r1b, Stat6, Pik3cd, Slc5a7, Chrm2 mainly involved in cAMP signaling, PI3K-Akt signaling, and JAK-STAT signaling pathways. The administration of RW-9 significantly upregulated the neurotransmitters including Serotonin (5-HT), Dopamine (DA), and Arginine (Arg) in mice brain. In addition, it modulated the serum metabolic profile and increased the expression levels of ATP-binding cassette (ABC) transporters, biosynthesis of amino acids, and Amino acyl-tRNA biosynthesis among others. Furthermore, 16s-rRNA results illustrated that the RW-9 restored the abundance of Muribaculaceae, <em>Lachnospiraceae</em>, <em>Lactobacillus, Clostridia</em> and <em>Bactericides</em>. Consistently, RW-9 restored the levels of SCFAs. Taken together, our results suggest that the RW-9 may prevent the AD like symptoms via modulation of gut-serum-brain axis.</div></div>","PeriodicalId":34393,"journal":{"name":"Journal of Agriculture and Food Research","volume":"24 ","pages":"Article 102394"},"PeriodicalIF":6.2000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Agriculture and Food Research","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666154325007653","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Oat protein-derived bioactive peptide (RW-9) has been reported to exert beneficial effects in memory deficits. However, the mechanisms underline the neuroprotective effects of RW-9 peptide against Alzheimer disease (AD) like symptoms remain unclear. In this study, we found that RW-9 intervention showed various improving effects in cognitive-behavioral tests and alleviated the oxidative stress and inflammation in scopolamine-induced mice model. The H&E staining results demonstrated the protective effects of RW-9 on hippocampal neurons. Proteomic analysis of hippocampus revealed the upregulation of memory related proteins, including Grin3a, Ppp2r1b, Stat6, Pik3cd, Slc5a7, Chrm2 mainly involved in cAMP signaling, PI3K-Akt signaling, and JAK-STAT signaling pathways. The administration of RW-9 significantly upregulated the neurotransmitters including Serotonin (5-HT), Dopamine (DA), and Arginine (Arg) in mice brain. In addition, it modulated the serum metabolic profile and increased the expression levels of ATP-binding cassette (ABC) transporters, biosynthesis of amino acids, and Amino acyl-tRNA biosynthesis among others. Furthermore, 16s-rRNA results illustrated that the RW-9 restored the abundance of Muribaculaceae, Lachnospiraceae, Lactobacillus, Clostridia and Bactericides. Consistently, RW-9 restored the levels of SCFAs. Taken together, our results suggest that the RW-9 may prevent the AD like symptoms via modulation of gut-serum-brain axis.