Lipids Alterations Associated with Metformin in Healthy Subjects: An Investigation Using Mass Spectrometry Shotgun Approach
Metformin is an orally effective insulin-sensitizing drug widely prescribed for treating type 2 diabetes mellitus (T2DM). Metformin has been reported to alter lipid metabolism. However, the molecular mechanisms behind its impact on lipid metabolism remain partially explored and understood. In the cu...
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Veröffentlicht in: | International journal of molecular sciences 2022-09, Vol.23 (19), p.11478 |
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creator | Dahabiyeh, Lina A. Mujammami, Muhammad AlMalki, Reem H. Arafat, Tawfiq Benabdelkamel, Hicham Alfadda, Assim A. Abdel Rahman, Anas M. |
description | Metformin is an orally effective insulin-sensitizing drug widely prescribed for treating type 2 diabetes mellitus (T2DM). Metformin has been reported to alter lipid metabolism. However, the molecular mechanisms behind its impact on lipid metabolism remain partially explored and understood. In the current study, mass spectrometry-based lipid profiling was used to investigate the lipidomic changes in the serum of 26 healthy individuals after a single-dose intake of metformin. Samples were analyzed at five-time points: preadministration, before the maximum concentration of metformin (Cmax), Cmax, after Cmax, and 36 h post-administration. A total of 762 molecules were significantly altered between the five-time points. Based on a comparison between baseline level and Cmax, metformin significantly increased and decreased the level of 33 and 192 lipids, respectively (FDR ≤ 0.05 and fold change cutoff of 1.5). The altered lipids are mainly involved in arachidonic acid metabolism, steroid hormone biosynthesis, and glycerophospholipid metabolism. Furthermore, several lipids acted in an opposed or similar manner to metformin levels and included fatty acyls, sterol lipids, glycerolipids, and glycerophospholipids. The significantly altered lipid species pointed to fundamental lipid signaling pathways that could be linked to the pleiotropic effects of metformin in T2DM, insulin resistance, polycystic ovary syndrome, cancer, and cardiovascular diseases. |
doi_str_mv | 10.3390/ijms231911478 |
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Metformin has been reported to alter lipid metabolism. However, the molecular mechanisms behind its impact on lipid metabolism remain partially explored and understood. In the current study, mass spectrometry-based lipid profiling was used to investigate the lipidomic changes in the serum of 26 healthy individuals after a single-dose intake of metformin. Samples were analyzed at five-time points: preadministration, before the maximum concentration of metformin (Cmax), Cmax, after Cmax, and 36 h post-administration. A total of 762 molecules were significantly altered between the five-time points. Based on a comparison between baseline level and Cmax, metformin significantly increased and decreased the level of 33 and 192 lipids, respectively (FDR ≤ 0.05 and fold change cutoff of 1.5). The altered lipids are mainly involved in arachidonic acid metabolism, steroid hormone biosynthesis, and glycerophospholipid metabolism. Furthermore, several lipids acted in an opposed or similar manner to metformin levels and included fatty acyls, sterol lipids, glycerolipids, and glycerophospholipids. The significantly altered lipid species pointed to fundamental lipid signaling pathways that could be linked to the pleiotropic effects of metformin in T2DM, insulin resistance, polycystic ovary syndrome, cancer, and cardiovascular diseases.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms231911478</identifier><identifier>PMID: 36232780</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Antidiabetics ; Arachidonic acid ; Biosynthesis ; Cardiovascular diseases ; Diabetes ; Diabetes mellitus ; Diabetes mellitus (non-insulin dependent) ; Glucose ; Insulin ; Insulin resistance ; Kinases ; Lipid metabolism ; Lipids ; Mass spectrometry ; Mass spectroscopy ; Metabolism ; Metabolites ; Metformin ; Molecular modelling ; Multivariate analysis ; Ovarian cancer ; Polycystic ovary syndrome ; Scientific imaging ; Shotguns ; Spectroscopy</subject><ispartof>International journal of molecular sciences, 2022-09, Vol.23 (19), p.11478</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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Metformin has been reported to alter lipid metabolism. However, the molecular mechanisms behind its impact on lipid metabolism remain partially explored and understood. In the current study, mass spectrometry-based lipid profiling was used to investigate the lipidomic changes in the serum of 26 healthy individuals after a single-dose intake of metformin. Samples were analyzed at five-time points: preadministration, before the maximum concentration of metformin (Cmax), Cmax, after Cmax, and 36 h post-administration. A total of 762 molecules were significantly altered between the five-time points. Based on a comparison between baseline level and Cmax, metformin significantly increased and decreased the level of 33 and 192 lipids, respectively (FDR ≤ 0.05 and fold change cutoff of 1.5). The altered lipids are mainly involved in arachidonic acid metabolism, steroid hormone biosynthesis, and glycerophospholipid metabolism. Furthermore, several lipids acted in an opposed or similar manner to metformin levels and included fatty acyls, sterol lipids, glycerolipids, and glycerophospholipids. The significantly altered lipid species pointed to fundamental lipid signaling pathways that could be linked to the pleiotropic effects of metformin in T2DM, insulin resistance, polycystic ovary syndrome, cancer, and cardiovascular diseases.</description><subject>Antidiabetics</subject><subject>Arachidonic acid</subject><subject>Biosynthesis</subject><subject>Cardiovascular diseases</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Glucose</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Kinases</subject><subject>Lipid metabolism</subject><subject>Lipids</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Metformin</subject><subject>Molecular modelling</subject><subject>Multivariate analysis</subject><subject>Ovarian cancer</subject><subject>Polycystic ovary syndrome</subject><subject>Scientific imaging</subject><subject>Shotguns</subject><subject>Spectroscopy</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkc1LHTEUxUOxVGu77D7gxs3YfE4SF8JD6gc86cK6DnmZzJs8ZpIxySjSf95YpdTChXvg_u7hHi4A3zA6oVSh7343ZUKxwpgJ-QEcYEZIg1Ar9v7R--BzzjuECCVcfQL7tK1KSHQAfq_97LsMV2NxyRQfQ9U5R-tNcR189GWAN670MU0-wFpXzoxleIK3y2bnbMmncBXgdXhwufjtHwN4l33YwhuTM7ydK5Pi5EqqK0Ms2yXA1TynaOzwBXzszZjd17d-CO4ufvw6v2rWPy-vz1frxlJCSiNx2zODsSSsR6KtQradk4gzRWUnsESOWkVZxwmxVFhqpSG9xNhwseGM0ENw9uo7L5vJddaFksyo5-Qnk550NF6_nwQ_6G180Iq3SkhZDY7fDFK8X2pSPfls3Tia4OKSNRGEY6U4YRU9-g_dxSWFGu-FYkRSzkWlmlfKpphzcv3fYzDSL2_V795KnwHBkJV5</recordid><startdate>20220929</startdate><enddate>20220929</enddate><creator>Dahabiyeh, Lina A.</creator><creator>Mujammami, Muhammad</creator><creator>AlMalki, Reem H.</creator><creator>Arafat, Tawfiq</creator><creator>Benabdelkamel, Hicham</creator><creator>Alfadda, Assim A.</creator><creator>Abdel Rahman, Anas M.</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5221-5634</orcidid><orcidid>https://orcid.org/0000-0002-4688-7052</orcidid><orcidid>https://orcid.org/0000-0002-9527-9424</orcidid><orcidid>https://orcid.org/0000-0001-9745-2959</orcidid><orcidid>https://orcid.org/0000-0002-4792-5188</orcidid></search><sort><creationdate>20220929</creationdate><title>Lipids Alterations Associated with Metformin in Healthy Subjects: An Investigation Using Mass Spectrometry Shotgun Approach</title><author>Dahabiyeh, Lina A. ; 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Metformin has been reported to alter lipid metabolism. However, the molecular mechanisms behind its impact on lipid metabolism remain partially explored and understood. In the current study, mass spectrometry-based lipid profiling was used to investigate the lipidomic changes in the serum of 26 healthy individuals after a single-dose intake of metformin. Samples were analyzed at five-time points: preadministration, before the maximum concentration of metformin (Cmax), Cmax, after Cmax, and 36 h post-administration. A total of 762 molecules were significantly altered between the five-time points. Based on a comparison between baseline level and Cmax, metformin significantly increased and decreased the level of 33 and 192 lipids, respectively (FDR ≤ 0.05 and fold change cutoff of 1.5). The altered lipids are mainly involved in arachidonic acid metabolism, steroid hormone biosynthesis, and glycerophospholipid metabolism. Furthermore, several lipids acted in an opposed or similar manner to metformin levels and included fatty acyls, sterol lipids, glycerolipids, and glycerophospholipids. The significantly altered lipid species pointed to fundamental lipid signaling pathways that could be linked to the pleiotropic effects of metformin in T2DM, insulin resistance, polycystic ovary syndrome, cancer, and cardiovascular diseases.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>36232780</pmid><doi>10.3390/ijms231911478</doi><orcidid>https://orcid.org/0000-0001-5221-5634</orcidid><orcidid>https://orcid.org/0000-0002-4688-7052</orcidid><orcidid>https://orcid.org/0000-0002-9527-9424</orcidid><orcidid>https://orcid.org/0000-0001-9745-2959</orcidid><orcidid>https://orcid.org/0000-0002-4792-5188</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antidiabetics Arachidonic acid Biosynthesis Cardiovascular diseases Diabetes Diabetes mellitus Diabetes mellitus (non-insulin dependent) Glucose Insulin Insulin resistance Kinases Lipid metabolism Lipids Mass spectrometry Mass spectroscopy Metabolism Metabolites Metformin Molecular modelling Multivariate analysis Ovarian cancer Polycystic ovary syndrome Scientific imaging Shotguns Spectroscopy |
title | Lipids Alterations Associated with Metformin in Healthy Subjects: An Investigation Using Mass Spectrometry Shotgun Approach |
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