Fenugreek extract improves diabetes-induced endothelial dysfunction via the arginase 1 pathway
Endothelial dysfunction (ED) is an initiating trigger and key factor in vascular complications, leading to disability and mortality in individuals with diabetes. The research concerning therapeutic interventions for ED has gained considerable interest. Fenugreek, a commonly used edible plant in diet...
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description | Endothelial dysfunction (ED) is an initiating trigger and key factor in vascular complications, leading to disability and mortality in individuals with diabetes. The research concerning therapeutic interventions for ED has gained considerable interest. Fenugreek, a commonly used edible plant in dietary consumption, has attracted significant attention due to its management of diabetes and its associated complications. The research presented in this study examines the potential therapeutic benefits of fenugreek in treating ED and investigates the underlying mechanism associated with its effects. The analysis on fenugreek was performed using 70% ethanol extract, and its chemical composition was analyzed using ultrahigh-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS). In total, we identified 49 compounds present in the fenugreek extract. These compounds encompass flavonoids, saponins, and phospholipids. Then, the models of ED in streptozotocin-induced diabetic mice and high glucose-induced isolated rat aortas were established for research. Through vascular function testing, it was observed that fenugreek extract effectively improved ED induced by diabetes or high glucose. By analyzing the protein expression of arginase 1 (Arg1), Arg activity, Arg1 immunohistochemistry, nitric oxide (NO) level, and the protein expression of endothelial nitric oxide synthase (eNOS), p38 mitogen-activated protein kinase (p38 MAPK), and p-p38 MAPK in aortas, this study revealed that the potential mechanism of fenugreek extract in anti-ED involves the downregulation of Arg1, leading to enhanced NO production. Furthermore, analysis of serum exosomes carrying Arg activity indicates that fenugreek may decrease the activity of Arg transported by serum exosomes, potentially preventing the increase in Arg levels triggered by the uptake of serum exosomes by vascular endothelial cells. In general, this investigation offers valuable observations regarding the curative impact of fenugreek extract on anti-ED in diabetes, revealing the involvement of the Arg1 pathway in its mechanism. |
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The research concerning therapeutic interventions for ED has gained considerable interest. Fenugreek, a commonly used edible plant in dietary consumption, has attracted significant attention due to its management of diabetes and its associated complications. The research presented in this study examines the potential therapeutic benefits of fenugreek in treating ED and investigates the underlying mechanism associated with its effects. The analysis on fenugreek was performed using 70% ethanol extract, and its chemical composition was analyzed using ultrahigh-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS). In total, we identified 49 compounds present in the fenugreek extract. These compounds encompass flavonoids, saponins, and phospholipids. Then, the models of ED in streptozotocin-induced diabetic mice and high glucose-induced isolated rat aortas were established for research. Through vascular function testing, it was observed that fenugreek extract effectively improved ED induced by diabetes or high glucose. By analyzing the protein expression of arginase 1 (Arg1), Arg activity, Arg1 immunohistochemistry, nitric oxide (NO) level, and the protein expression of endothelial nitric oxide synthase (eNOS), p38 mitogen-activated protein kinase (p38 MAPK), and p-p38 MAPK in aortas, this study revealed that the potential mechanism of fenugreek extract in anti-ED involves the downregulation of Arg1, leading to enhanced NO production. Furthermore, analysis of serum exosomes carrying Arg activity indicates that fenugreek may decrease the activity of Arg transported by serum exosomes, potentially preventing the increase in Arg levels triggered by the uptake of serum exosomes by vascular endothelial cells. In general, this investigation offers valuable observations regarding the curative impact of fenugreek extract on anti-ED in diabetes, revealing the involvement of the Arg1 pathway in its mechanism.</description><identifier>ISSN: 2042-6496</identifier><identifier>EISSN: 2042-650X</identifier><identifier>DOI: 10.1039/d3fo04283a</identifier><identifier>PMID: 38450419</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Animals ; Arginase ; Chemical composition ; Chromatography ; Diabetes ; Diabetes mellitus ; Diabetes Mellitus, Experimental - drug therapy ; Diabetes Mellitus, Experimental - metabolism ; Endothelial Cells ; Ethanol ; Exosomes ; Fenugreek ; Flavonoids ; Glucose ; Glucose - metabolism ; Immunohistochemistry ; Kinases ; Liquid chromatography ; MAP kinase ; Mass spectrometry ; Mass spectroscopy ; Mice ; Nitric oxide ; Nitric Oxide Synthase Type III - metabolism ; Nitric-oxide synthase ; p38 Mitogen-Activated Protein Kinases - metabolism ; Phospholipids ; Plant Extracts ; Protein expression ; Proteins ; Quadrupoles ; Rats ; Saponins ; Serum ; Streptozocin ; Therapeutic applications ; Trigonella ; Trigonella foenum-graecum</subject><ispartof>Food & function, 2024-04, Vol.15 (7), p.3446-3462</ispartof><rights>Copyright Royal Society of Chemistry 2024</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c274t-bfe4fda6530661810b7dd76b6354e6a748b93486c641befc8d6bc921051f9bbb3</cites><orcidid>0000-0003-1986-2279</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38450419$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qiu, Dingbang</creatorcontrib><creatorcontrib>Hu, Jinxin</creatorcontrib><creatorcontrib>Zhang, Shaoying</creatorcontrib><creatorcontrib>Cai, Wanjun</creatorcontrib><creatorcontrib>Miao, Jingwei</creatorcontrib><creatorcontrib>Li, Pengdong</creatorcontrib><creatorcontrib>Jiang, Wenyue</creatorcontrib><title>Fenugreek extract improves diabetes-induced endothelial dysfunction via the arginase 1 pathway</title><title>Food & function</title><addtitle>Food Funct</addtitle><description>Endothelial dysfunction (ED) is an initiating trigger and key factor in vascular complications, leading to disability and mortality in individuals with diabetes. The research concerning therapeutic interventions for ED has gained considerable interest. Fenugreek, a commonly used edible plant in dietary consumption, has attracted significant attention due to its management of diabetes and its associated complications. The research presented in this study examines the potential therapeutic benefits of fenugreek in treating ED and investigates the underlying mechanism associated with its effects. The analysis on fenugreek was performed using 70% ethanol extract, and its chemical composition was analyzed using ultrahigh-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS). In total, we identified 49 compounds present in the fenugreek extract. These compounds encompass flavonoids, saponins, and phospholipids. Then, the models of ED in streptozotocin-induced diabetic mice and high glucose-induced isolated rat aortas were established for research. Through vascular function testing, it was observed that fenugreek extract effectively improved ED induced by diabetes or high glucose. By analyzing the protein expression of arginase 1 (Arg1), Arg activity, Arg1 immunohistochemistry, nitric oxide (NO) level, and the protein expression of endothelial nitric oxide synthase (eNOS), p38 mitogen-activated protein kinase (p38 MAPK), and p-p38 MAPK in aortas, this study revealed that the potential mechanism of fenugreek extract in anti-ED involves the downregulation of Arg1, leading to enhanced NO production. Furthermore, analysis of serum exosomes carrying Arg activity indicates that fenugreek may decrease the activity of Arg transported by serum exosomes, potentially preventing the increase in Arg levels triggered by the uptake of serum exosomes by vascular endothelial cells. In general, this investigation offers valuable observations regarding the curative impact of fenugreek extract on anti-ED in diabetes, revealing the involvement of the Arg1 pathway in its mechanism.</description><subject>Animals</subject><subject>Arginase</subject><subject>Chemical composition</subject><subject>Chromatography</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus, Experimental - drug therapy</subject><subject>Diabetes Mellitus, Experimental - metabolism</subject><subject>Endothelial Cells</subject><subject>Ethanol</subject><subject>Exosomes</subject><subject>Fenugreek</subject><subject>Flavonoids</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>Immunohistochemistry</subject><subject>Kinases</subject><subject>Liquid chromatography</subject><subject>MAP kinase</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Mice</subject><subject>Nitric oxide</subject><subject>Nitric Oxide Synthase Type III - metabolism</subject><subject>Nitric-oxide synthase</subject><subject>p38 Mitogen-Activated Protein Kinases - metabolism</subject><subject>Phospholipids</subject><subject>Plant Extracts</subject><subject>Protein expression</subject><subject>Proteins</subject><subject>Quadrupoles</subject><subject>Rats</subject><subject>Saponins</subject><subject>Serum</subject><subject>Streptozocin</subject><subject>Therapeutic applications</subject><subject>Trigonella</subject><subject>Trigonella foenum-graecum</subject><issn>2042-6496</issn><issn>2042-650X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkE9LxDAQxYMo7qJ78QNIwIsI1aRJ0-S4qKuCsBcFT5b8mWq0265Ju7rf3qirB-cyj-HHm8dD6ICSU0qYOnOs7gjPJdNbaJwnlYmCPGz_aq7ECE1ifCFpmFJSyV00YpIXhFM1Ro8zaIenAPCK4aMP2vbYL5ahW0HEzmsDPcTMt26w4DC0ruufofG6wW4d66G1ve9avPIapzvW4cm3OgKmeKn753e93kc7tW4iTDZ7D93PLu_Or7Pb-dXN-fQ2s3nJ-8zUwGunRcGIEFRSYkrnSmEEKzgIXXJpFONSWMGpgdpKJ4xVOSUFrZUxhu2h4x_fFP1tgNhXCx8tNI1uoRtilSueUykplwk9-oe-dENoU7qKkfRf5iVjiTr5oWzoYgxQV8vgFzqsK0qqr-KrCzabfxc_TfDhxnIwC3B_6G_N7BMyRH4e</recordid><startdate>20240402</startdate><enddate>20240402</enddate><creator>Qiu, Dingbang</creator><creator>Hu, Jinxin</creator><creator>Zhang, Shaoying</creator><creator>Cai, Wanjun</creator><creator>Miao, Jingwei</creator><creator>Li, Pengdong</creator><creator>Jiang, Wenyue</creator><general>Royal Society of Chemistry</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7T7</scope><scope>7TO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1986-2279</orcidid></search><sort><creationdate>20240402</creationdate><title>Fenugreek extract improves diabetes-induced endothelial dysfunction via the arginase 1 pathway</title><author>Qiu, Dingbang ; Hu, Jinxin ; Zhang, Shaoying ; Cai, Wanjun ; Miao, Jingwei ; Li, Pengdong ; Jiang, Wenyue</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c274t-bfe4fda6530661810b7dd76b6354e6a748b93486c641befc8d6bc921051f9bbb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Arginase</topic><topic>Chemical composition</topic><topic>Chromatography</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus, Experimental - drug therapy</topic><topic>Diabetes Mellitus, Experimental - metabolism</topic><topic>Endothelial Cells</topic><topic>Ethanol</topic><topic>Exosomes</topic><topic>Fenugreek</topic><topic>Flavonoids</topic><topic>Glucose</topic><topic>Glucose - metabolism</topic><topic>Immunohistochemistry</topic><topic>Kinases</topic><topic>Liquid chromatography</topic><topic>MAP kinase</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Mice</topic><topic>Nitric oxide</topic><topic>Nitric Oxide Synthase Type III - metabolism</topic><topic>Nitric-oxide synthase</topic><topic>p38 Mitogen-Activated Protein Kinases - metabolism</topic><topic>Phospholipids</topic><topic>Plant Extracts</topic><topic>Protein expression</topic><topic>Proteins</topic><topic>Quadrupoles</topic><topic>Rats</topic><topic>Saponins</topic><topic>Serum</topic><topic>Streptozocin</topic><topic>Therapeutic applications</topic><topic>Trigonella</topic><topic>Trigonella foenum-graecum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qiu, Dingbang</creatorcontrib><creatorcontrib>Hu, Jinxin</creatorcontrib><creatorcontrib>Zhang, Shaoying</creatorcontrib><creatorcontrib>Cai, Wanjun</creatorcontrib><creatorcontrib>Miao, Jingwei</creatorcontrib><creatorcontrib>Li, Pengdong</creatorcontrib><creatorcontrib>Jiang, Wenyue</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Food & function</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qiu, Dingbang</au><au>Hu, Jinxin</au><au>Zhang, Shaoying</au><au>Cai, Wanjun</au><au>Miao, Jingwei</au><au>Li, Pengdong</au><au>Jiang, Wenyue</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fenugreek extract improves diabetes-induced endothelial dysfunction via the arginase 1 pathway</atitle><jtitle>Food & function</jtitle><addtitle>Food Funct</addtitle><date>2024-04-02</date><risdate>2024</risdate><volume>15</volume><issue>7</issue><spage>3446</spage><epage>3462</epage><pages>3446-3462</pages><issn>2042-6496</issn><eissn>2042-650X</eissn><abstract>Endothelial dysfunction (ED) is an initiating trigger and key factor in vascular complications, leading to disability and mortality in individuals with diabetes. The research concerning therapeutic interventions for ED has gained considerable interest. Fenugreek, a commonly used edible plant in dietary consumption, has attracted significant attention due to its management of diabetes and its associated complications. The research presented in this study examines the potential therapeutic benefits of fenugreek in treating ED and investigates the underlying mechanism associated with its effects. The analysis on fenugreek was performed using 70% ethanol extract, and its chemical composition was analyzed using ultrahigh-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS). In total, we identified 49 compounds present in the fenugreek extract. These compounds encompass flavonoids, saponins, and phospholipids. Then, the models of ED in streptozotocin-induced diabetic mice and high glucose-induced isolated rat aortas were established for research. Through vascular function testing, it was observed that fenugreek extract effectively improved ED induced by diabetes or high glucose. By analyzing the protein expression of arginase 1 (Arg1), Arg activity, Arg1 immunohistochemistry, nitric oxide (NO) level, and the protein expression of endothelial nitric oxide synthase (eNOS), p38 mitogen-activated protein kinase (p38 MAPK), and p-p38 MAPK in aortas, this study revealed that the potential mechanism of fenugreek extract in anti-ED involves the downregulation of Arg1, leading to enhanced NO production. Furthermore, analysis of serum exosomes carrying Arg activity indicates that fenugreek may decrease the activity of Arg transported by serum exosomes, potentially preventing the increase in Arg levels triggered by the uptake of serum exosomes by vascular endothelial cells. In general, this investigation offers valuable observations regarding the curative impact of fenugreek extract on anti-ED in diabetes, revealing the involvement of the Arg1 pathway in its mechanism.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>38450419</pmid><doi>10.1039/d3fo04283a</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0003-1986-2279</orcidid></addata></record> |
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subjects | Animals Arginase Chemical composition Chromatography Diabetes Diabetes mellitus Diabetes Mellitus, Experimental - drug therapy Diabetes Mellitus, Experimental - metabolism Endothelial Cells Ethanol Exosomes Fenugreek Flavonoids Glucose Glucose - metabolism Immunohistochemistry Kinases Liquid chromatography MAP kinase Mass spectrometry Mass spectroscopy Mice Nitric oxide Nitric Oxide Synthase Type III - metabolism Nitric-oxide synthase p38 Mitogen-Activated Protein Kinases - metabolism Phospholipids Plant Extracts Protein expression Proteins Quadrupoles Rats Saponins Serum Streptozocin Therapeutic applications Trigonella Trigonella foenum-graecum |
title | Fenugreek extract improves diabetes-induced endothelial dysfunction via the arginase 1 pathway |
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