Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Highland barley has shown potential in regulating blood glucose and may serve as a natural source of dipeptidyl peptidase-IV (DPP-IV) inhibitors. In this study, machine learning (Gradient Boosting Decision Trees) and virtual screening were employed to identify DPP-IV inhibitory peptides from highland barley protein. Three candidate peptides (FPQPQ, FPRPF, and YGGWN) had IC of 675.47, 766.80, and 281.76 μM, respectively. FPQPQ and FPRPF are competitive DPP-IV inhibitors, whereas YGGWN is a non-competitive inhibitor. Their inhibitory mechanisms were investigated through molecular docking, and molecular dynamics simulations. Network pharmacology was applied to reveal their multitarget and multipathway antihyperglycaemic activities in vivo. This integrated approach enabled efficient and precise screening of bioactive peptides and provided mechanistic insights into their inhibitory effects. The findings demonstrate the potential of these peptides in glucose regulation and support the development of functional foods based on highland barley protein.
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http://dx.doi.org/10.1016/j.foodchem.2025.144979 | DOI Listing |