Plasma 3-hydroxyisobutyrate (3-HIB) and methylmalonic acid (MMA) are markers of hepatic mitochondrial fatty acid oxidation in male Wistar rats
Discovery of specific markers that reflect altered hepatic fatty acid oxidation could help to detect an individual's risk of fatty liver, type 2 diabetes and cardiovascular disease at an early stage. Lipid and protein metabolism are intimately linked, but our understanding of this crosstalk rem...
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creator | Bjune, Mona Synnøve Lindquist, Carine Hallvardsdotter Stafsnes, Marit Bjørndal, Bodil Bruheim, Per Aloysius, Thomas A. Nygård, Ottar Skorve, Jon Madsen, Lise Dankel, Simon N. Berge, Rolf Kristian |
description | Discovery of specific markers that reflect altered hepatic fatty acid oxidation could help to detect an individual's risk of fatty liver, type 2 diabetes and cardiovascular disease at an early stage. Lipid and protein metabolism are intimately linked, but our understanding of this crosstalk remains limited.
In male Wistar rats, we used synthetic fatty acid analogues (3-thia fatty acids) as a tool to induce hepatic fatty acid oxidation and mitochondrial biogenesis, to gain new insight into the link between fatty acid oxidation, amino acid metabolism and TCA cycle-related intermediate metabolites in liver and plasma.
Rats treated with 3-thia fatty acids had 3-fold higher hepatic, but not adipose and skeletal muscle, expression of the thioesterase 3-hydroxyisobutyryl-CoA hydrolase (Hibch), which controls the formation of 3-hydroxyisobutyrate (3-HIB) in the valine degradation pathway. Consequently, 3-thia fatty acid-stimulated hepatic fatty acid oxidation and ketogenesis was accompanied by decreased plasma 3-HIB and increased methylmalonic acid (MMA) concentrations further downstream in BCAA catabolism. The higher plasma MMA corresponded to higher MMA-CoA hydrolase activity and hepatic expression of GTP-specific succinyl-CoA synthase (Suclg2) and succinate dehydrogenase (Sdhb), and lower MMA-CoA mutase activity. Plasma 3-HIB correlated positively to plasma and hepatic concentrations of TAG, plasma total fatty acids, plasma NEFA and insulin/glucose ratio, while the reverse correlations were seen for MMA.
Our study provides new insight into TCA cycle-related metabolic changes associated with altered hepatic fatty acid flux, and identifies 3-HIB and MMA as novel circulating markers reflective of mitochondrial β-oxidation in male Wistar rats.
•3-Thia fatty acids (FA) promote mitochondrial β-oxidation and insulin sensitivity.•3-Thia FA upregulate Hibch expression in liver but not in adipose and muscle tissue.•3-Thia FA decrease 3-HIB and increase MMA and succinate levels in plasma.•Plasma 3-HIB and MMA are markers of hepatic mitochondrial fatty acid β-oxidation. |
doi_str_mv | 10.1016/j.bbalip.2021.158887 |
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In male Wistar rats, we used synthetic fatty acid analogues (3-thia fatty acids) as a tool to induce hepatic fatty acid oxidation and mitochondrial biogenesis, to gain new insight into the link between fatty acid oxidation, amino acid metabolism and TCA cycle-related intermediate metabolites in liver and plasma.
Rats treated with 3-thia fatty acids had 3-fold higher hepatic, but not adipose and skeletal muscle, expression of the thioesterase 3-hydroxyisobutyryl-CoA hydrolase (Hibch), which controls the formation of 3-hydroxyisobutyrate (3-HIB) in the valine degradation pathway. Consequently, 3-thia fatty acid-stimulated hepatic fatty acid oxidation and ketogenesis was accompanied by decreased plasma 3-HIB and increased methylmalonic acid (MMA) concentrations further downstream in BCAA catabolism. The higher plasma MMA corresponded to higher MMA-CoA hydrolase activity and hepatic expression of GTP-specific succinyl-CoA synthase (Suclg2) and succinate dehydrogenase (Sdhb), and lower MMA-CoA mutase activity. Plasma 3-HIB correlated positively to plasma and hepatic concentrations of TAG, plasma total fatty acids, plasma NEFA and insulin/glucose ratio, while the reverse correlations were seen for MMA.
Our study provides new insight into TCA cycle-related metabolic changes associated with altered hepatic fatty acid flux, and identifies 3-HIB and MMA as novel circulating markers reflective of mitochondrial β-oxidation in male Wistar rats.
•3-Thia fatty acids (FA) promote mitochondrial β-oxidation and insulin sensitivity.•3-Thia FA upregulate Hibch expression in liver but not in adipose and muscle tissue.•3-Thia FA decrease 3-HIB and increase MMA and succinate levels in plasma.•Plasma 3-HIB and MMA are markers of hepatic mitochondrial fatty acid β-oxidation.</description><identifier>ISSN: 1388-1981</identifier><identifier>EISSN: 1879-2618</identifier><identifier>DOI: 10.1016/j.bbalip.2021.158887</identifier><identifier>PMID: 33454435</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>3-Hydroxisobutyrate ; Animals ; BCAA ; Fatty acid β-oxidation ; Fatty Acids - metabolism ; Hydroxybutyrates - blood ; Hydroxybutyrates - metabolism ; Insulin Resistance ; Male ; Methylmalonic acid ; Methylmalonic Acid - blood ; Methylmalonic Acid - metabolism ; Mitochondria, Liver - metabolism ; Oxidation-Reduction ; Rats ; Rats, Wistar ; TCA cycle</subject><ispartof>Biochimica et biophysica acta. Molecular and cell biology of lipids, 2021-04, Vol.1866 (4), p.158887-158887, Article 158887</ispartof><rights>2021</rights><rights>Copyright © 2021. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-af79d54387fe8b3382883a11a03faa8c43847e38fd4294bea7ea3b10a86cbbbc3</citedby><cites>FETCH-LOGICAL-c408t-af79d54387fe8b3382883a11a03faa8c43847e38fd4294bea7ea3b10a86cbbbc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bbalip.2021.158887$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33454435$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bjune, Mona Synnøve</creatorcontrib><creatorcontrib>Lindquist, Carine</creatorcontrib><creatorcontrib>Hallvardsdotter Stafsnes, Marit</creatorcontrib><creatorcontrib>Bjørndal, Bodil</creatorcontrib><creatorcontrib>Bruheim, Per</creatorcontrib><creatorcontrib>Aloysius, Thomas A.</creatorcontrib><creatorcontrib>Nygård, Ottar</creatorcontrib><creatorcontrib>Skorve, Jon</creatorcontrib><creatorcontrib>Madsen, Lise</creatorcontrib><creatorcontrib>Dankel, Simon N.</creatorcontrib><creatorcontrib>Berge, Rolf Kristian</creatorcontrib><title>Plasma 3-hydroxyisobutyrate (3-HIB) and methylmalonic acid (MMA) are markers of hepatic mitochondrial fatty acid oxidation in male Wistar rats</title><title>Biochimica et biophysica acta. Molecular and cell biology of lipids</title><addtitle>Biochim Biophys Acta Mol Cell Biol Lipids</addtitle><description>Discovery of specific markers that reflect altered hepatic fatty acid oxidation could help to detect an individual's risk of fatty liver, type 2 diabetes and cardiovascular disease at an early stage. Lipid and protein metabolism are intimately linked, but our understanding of this crosstalk remains limited.
In male Wistar rats, we used synthetic fatty acid analogues (3-thia fatty acids) as a tool to induce hepatic fatty acid oxidation and mitochondrial biogenesis, to gain new insight into the link between fatty acid oxidation, amino acid metabolism and TCA cycle-related intermediate metabolites in liver and plasma.
Rats treated with 3-thia fatty acids had 3-fold higher hepatic, but not adipose and skeletal muscle, expression of the thioesterase 3-hydroxyisobutyryl-CoA hydrolase (Hibch), which controls the formation of 3-hydroxyisobutyrate (3-HIB) in the valine degradation pathway. Consequently, 3-thia fatty acid-stimulated hepatic fatty acid oxidation and ketogenesis was accompanied by decreased plasma 3-HIB and increased methylmalonic acid (MMA) concentrations further downstream in BCAA catabolism. The higher plasma MMA corresponded to higher MMA-CoA hydrolase activity and hepatic expression of GTP-specific succinyl-CoA synthase (Suclg2) and succinate dehydrogenase (Sdhb), and lower MMA-CoA mutase activity. Plasma 3-HIB correlated positively to plasma and hepatic concentrations of TAG, plasma total fatty acids, plasma NEFA and insulin/glucose ratio, while the reverse correlations were seen for MMA.
Our study provides new insight into TCA cycle-related metabolic changes associated with altered hepatic fatty acid flux, and identifies 3-HIB and MMA as novel circulating markers reflective of mitochondrial β-oxidation in male Wistar rats.
•3-Thia fatty acids (FA) promote mitochondrial β-oxidation and insulin sensitivity.•3-Thia FA upregulate Hibch expression in liver but not in adipose and muscle tissue.•3-Thia FA decrease 3-HIB and increase MMA and succinate levels in plasma.•Plasma 3-HIB and MMA are markers of hepatic mitochondrial fatty acid β-oxidation.</description><subject>3-Hydroxisobutyrate</subject><subject>Animals</subject><subject>BCAA</subject><subject>Fatty acid β-oxidation</subject><subject>Fatty Acids - metabolism</subject><subject>Hydroxybutyrates - blood</subject><subject>Hydroxybutyrates - metabolism</subject><subject>Insulin Resistance</subject><subject>Male</subject><subject>Methylmalonic acid</subject><subject>Methylmalonic Acid - blood</subject><subject>Methylmalonic Acid - metabolism</subject><subject>Mitochondria, Liver - metabolism</subject><subject>Oxidation-Reduction</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>TCA cycle</subject><issn>1388-1981</issn><issn>1879-2618</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kctuFDEQRVsIRB7wBwh5OSx68KvHng1SEhESKREsQCytsl2t8dDdHmwPSv8E34yjDixZVUl1bl1V3aZ5w-iaUbZ5v19bC0M4rDnlbM06rbV61pwyrbYt3zD9vPZC65ZtNTtpznLeU8o6IbqXzYkQspNSdKfN7y8D5BGIaHezT_FhDjnaY5kTFCQr0d7cXr4jMHkyYtnNwwhDnIIj4IInq_v7izpMSEZIPzBlEnuywwOUSoyhRLeLk08BBtJDKfOiig_BVyJOJExVOCD5HnKBRKplftW86GHI-Pqpnjffrj9-vbpp7z5_ur26uGudpLq00Kut76TQqkdthdBcawGMARU9gHZ1IhUK3XvJt9IiKARhGQW9cdZaJ86b1bL3kOLPI-ZixpAdDgNMGI_ZcKm0UpxzUVG5oC7FnBP25pBCPXg2jJrHJMzeLEmYxyTMkkSVvX1yONoR_T_R39dX4MMCYL3zV8Bksgs4OfQhoSvGx_B_hz8tNJz0</recordid><startdate>202104</startdate><enddate>202104</enddate><creator>Bjune, Mona Synnøve</creator><creator>Lindquist, Carine</creator><creator>Hallvardsdotter Stafsnes, Marit</creator><creator>Bjørndal, Bodil</creator><creator>Bruheim, Per</creator><creator>Aloysius, Thomas A.</creator><creator>Nygård, Ottar</creator><creator>Skorve, Jon</creator><creator>Madsen, Lise</creator><creator>Dankel, Simon N.</creator><creator>Berge, Rolf Kristian</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope></search><sort><creationdate>202104</creationdate><title>Plasma 3-hydroxyisobutyrate (3-HIB) and methylmalonic acid (MMA) are markers of hepatic mitochondrial fatty acid oxidation in male Wistar rats</title><author>Bjune, Mona Synnøve ; Lindquist, Carine ; Hallvardsdotter Stafsnes, Marit ; Bjørndal, Bodil ; Bruheim, Per ; Aloysius, Thomas A. ; Nygård, Ottar ; Skorve, Jon ; Madsen, Lise ; Dankel, Simon N. ; Berge, Rolf Kristian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-af79d54387fe8b3382883a11a03faa8c43847e38fd4294bea7ea3b10a86cbbbc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>3-Hydroxisobutyrate</topic><topic>Animals</topic><topic>BCAA</topic><topic>Fatty acid β-oxidation</topic><topic>Fatty Acids - metabolism</topic><topic>Hydroxybutyrates - blood</topic><topic>Hydroxybutyrates - metabolism</topic><topic>Insulin Resistance</topic><topic>Male</topic><topic>Methylmalonic acid</topic><topic>Methylmalonic Acid - blood</topic><topic>Methylmalonic Acid - metabolism</topic><topic>Mitochondria, Liver - metabolism</topic><topic>Oxidation-Reduction</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>TCA cycle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bjune, Mona Synnøve</creatorcontrib><creatorcontrib>Lindquist, Carine</creatorcontrib><creatorcontrib>Hallvardsdotter Stafsnes, Marit</creatorcontrib><creatorcontrib>Bjørndal, Bodil</creatorcontrib><creatorcontrib>Bruheim, Per</creatorcontrib><creatorcontrib>Aloysius, Thomas A.</creatorcontrib><creatorcontrib>Nygård, Ottar</creatorcontrib><creatorcontrib>Skorve, Jon</creatorcontrib><creatorcontrib>Madsen, Lise</creatorcontrib><creatorcontrib>Dankel, Simon N.</creatorcontrib><creatorcontrib>Berge, Rolf Kristian</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochimica et biophysica acta. 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Molecular and cell biology of lipids</jtitle><addtitle>Biochim Biophys Acta Mol Cell Biol Lipids</addtitle><date>2021-04</date><risdate>2021</risdate><volume>1866</volume><issue>4</issue><spage>158887</spage><epage>158887</epage><pages>158887-158887</pages><artnum>158887</artnum><issn>1388-1981</issn><eissn>1879-2618</eissn><abstract>Discovery of specific markers that reflect altered hepatic fatty acid oxidation could help to detect an individual's risk of fatty liver, type 2 diabetes and cardiovascular disease at an early stage. Lipid and protein metabolism are intimately linked, but our understanding of this crosstalk remains limited.
In male Wistar rats, we used synthetic fatty acid analogues (3-thia fatty acids) as a tool to induce hepatic fatty acid oxidation and mitochondrial biogenesis, to gain new insight into the link between fatty acid oxidation, amino acid metabolism and TCA cycle-related intermediate metabolites in liver and plasma.
Rats treated with 3-thia fatty acids had 3-fold higher hepatic, but not adipose and skeletal muscle, expression of the thioesterase 3-hydroxyisobutyryl-CoA hydrolase (Hibch), which controls the formation of 3-hydroxyisobutyrate (3-HIB) in the valine degradation pathway. Consequently, 3-thia fatty acid-stimulated hepatic fatty acid oxidation and ketogenesis was accompanied by decreased plasma 3-HIB and increased methylmalonic acid (MMA) concentrations further downstream in BCAA catabolism. The higher plasma MMA corresponded to higher MMA-CoA hydrolase activity and hepatic expression of GTP-specific succinyl-CoA synthase (Suclg2) and succinate dehydrogenase (Sdhb), and lower MMA-CoA mutase activity. Plasma 3-HIB correlated positively to plasma and hepatic concentrations of TAG, plasma total fatty acids, plasma NEFA and insulin/glucose ratio, while the reverse correlations were seen for MMA.
Our study provides new insight into TCA cycle-related metabolic changes associated with altered hepatic fatty acid flux, and identifies 3-HIB and MMA as novel circulating markers reflective of mitochondrial β-oxidation in male Wistar rats.
•3-Thia fatty acids (FA) promote mitochondrial β-oxidation and insulin sensitivity.•3-Thia FA upregulate Hibch expression in liver but not in adipose and muscle tissue.•3-Thia FA decrease 3-HIB and increase MMA and succinate levels in plasma.•Plasma 3-HIB and MMA are markers of hepatic mitochondrial fatty acid β-oxidation.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>33454435</pmid><doi>10.1016/j.bbalip.2021.158887</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3-Hydroxisobutyrate Animals BCAA Fatty acid β-oxidation Fatty Acids - metabolism Hydroxybutyrates - blood Hydroxybutyrates - metabolism Insulin Resistance Male Methylmalonic acid Methylmalonic Acid - blood Methylmalonic Acid - metabolism Mitochondria, Liver - metabolism Oxidation-Reduction Rats Rats, Wistar TCA cycle |
title | Plasma 3-hydroxyisobutyrate (3-HIB) and methylmalonic acid (MMA) are markers of hepatic mitochondrial fatty acid oxidation in male Wistar rats |
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