<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16</volume><submitter>Niu Y</submitter><pubmed_abstract>&lt;h4>Objectives&lt;/h4>&lt;i>Trigonella foenum-graecum&lt;/i> L. (HLB) exhibits promising pharmacological properties for the treatment of type 2 diabetic nephropathy (DN). This study aims to enhance the understanding of HLB's pharmacodynamic effects and elucidate the mechanisms underlying its therapeutic potential in DN.&lt;h4>Methods&lt;/h4>The pharmacodynamic effects of HLB were initially evaluated in a murine DN model through the oral administration of an aqueous extract of HLB. The primary bioactive constituents were subsequently identified using ultra-high-performance liquid chromatography coupled with high-resolution mass spectrometry (UHPLC-HRMS). Network pharmacology analysis was integrated with these data to uncover potential molecular targets of HLB in DN. Key renal metabolites were profiled usi</pubmed_abstract><journal>Frontiers in pharmacology</journal><pagination>1566723</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11959092</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&amp;lt;i&amp;gt;Trigonella foenum-graecum&amp;lt;/i&amp;gt; L. protects against renal function decline in a mouse model of type 2 diabetic nephropathy by modulating the PI3K-Akt-ERK signaling pathway.</pubmed_title><pmcid>PMC11959092</pmcid><pubmed_authors>Chi L</pubmed_authors><pubmed_authors>He X</pubmed_authors><pubmed_authors>Li P</pubmed_authors><pubmed_authors>Pang Z</pubmed_authors><pubmed_authors>Du J</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Niu H</pubmed_authors><pubmed_authors>Niu Y</pubmed_authors><pubmed_authors>Lu B</pubmed_authors></additional><is_claimable>false</is_claimable><name>&amp;lt;i&amp;gt;Trigonella foenum-graecum&amp;lt;/i&amp;gt; L. protects against renal function decline in a mouse model of type 2 diabetic nephropathy by modulating the PI3K-Akt-ERK signaling pathway.</name><description>&lt;h4>Objectives&lt;/h4>&lt;i>Trigonella foenum-graecum&lt;/i> L. (HLB) exhibits promising pharmacological properties for the treatment of type 2 diabetic nephropathy (DN). This study aims to enhance the understanding of HLB's pharmacodynamic effects and elucidate the mechanisms underlying its therapeutic potential in DN.&lt;h4>Methods&lt;/h4>The pharmacodynamic effects of HLB were initially evaluated in a murine DN model through the oral administration of an aqueous extract of HLB. The primary bioactive constituents were subsequently identified using ultra-high-performance liquid chromatography coupled with high-resolution mass spectrometry (UHPLC-HRMS). Network pharmacology analysis was integrated with these data to uncover potential molecular targets of HLB in DN. Key renal metabolites were profiled usi</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2025-07-11T03:04:03.998Z</modification><creation>2025-07-11T03:04:03.998Z</creation></dates><accession>S-EPMC11959092</accession><cross_references><pubmed>40170727</pubmed><doi>10.3389/fphar.2025.1566723</doi></cross_references></HashMap>