Saturated fatty acid-induced insulin resistance is associated with mitochondrial dysfunction in skeletal muscle cells
Increased plasma levels of free fatty acids (FFA) occur in states of insulin resistance such as obesity and type 2 diabetes mellitus. These high levels of plasma FFA are proposed to play an important role for the development of insulin resistance but the mechanisms involved are still unclear. This s...
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Veröffentlicht in: | Journal of cellular physiology 2010-01, Vol.222 (1), p.187-194 |
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description | Increased plasma levels of free fatty acids (FFA) occur in states of insulin resistance such as obesity and type 2 diabetes mellitus. These high levels of plasma FFA are proposed to play an important role for the development of insulin resistance but the mechanisms involved are still unclear. This study investigated the effects of saturated and unsaturated FFA on insulin sensitivity in parallel with mitochondrial function. C2C12 myotubes were treated for 24 h with 0.1 mM of saturated (palmitic and stearic) and unsaturated (oleic, linoleic, eicosapentaenoic, and docosahexaenoic) FFA. After this period, basal and insulin‐stimulated glucose metabolism and mitochondrial function were evaluated. Saturated palmitic and stearic acids decreased insulin‐induced glycogen synthesis, glucose oxidation, and lactate production. Basal glucose oxidation was also reduced. Palmitic and stearic acids impaired mitochondrial function as demonstrated by decrease of both mitochondrial hyperpolarization and ATP generation. These FFA also decreased Akt activation by insulin. As opposed to saturated FFA, unsaturated FFA did not impair glucose metabolism and mitochondrial function. Primary cultures of rat skeletal muscle cells exhibited similar responses to saturated FFA as compared to C2C12 cells. These results show that in muscle cells saturated FFA‐induced mitochondrial dysfunction associated with impaired insulin‐induced glucose metabolism. J. Cell. Physiol. 222:187–194, 2010. © 2009 Wiley‐Liss, Inc. |
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These high levels of plasma FFA are proposed to play an important role for the development of insulin resistance but the mechanisms involved are still unclear. This study investigated the effects of saturated and unsaturated FFA on insulin sensitivity in parallel with mitochondrial function. C2C12 myotubes were treated for 24 h with 0.1 mM of saturated (palmitic and stearic) and unsaturated (oleic, linoleic, eicosapentaenoic, and docosahexaenoic) FFA. After this period, basal and insulin‐stimulated glucose metabolism and mitochondrial function were evaluated. Saturated palmitic and stearic acids decreased insulin‐induced glycogen synthesis, glucose oxidation, and lactate production. Basal glucose oxidation was also reduced. Palmitic and stearic acids impaired mitochondrial function as demonstrated by decrease of both mitochondrial hyperpolarization and ATP generation. These FFA also decreased Akt activation by insulin. As opposed to saturated FFA, unsaturated FFA did not impair glucose metabolism and mitochondrial function. Primary cultures of rat skeletal muscle cells exhibited similar responses to saturated FFA as compared to C2C12 cells. These results show that in muscle cells saturated FFA‐induced mitochondrial dysfunction associated with impaired insulin‐induced glucose metabolism. J. Cell. Physiol. 222:187–194, 2010. © 2009 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.21936</identifier><identifier>PMID: 19780047</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adenosine Triphosphate - biosynthesis ; Animals ; Cell Survival - drug effects ; Cells, Cultured ; Fatty Acids - pharmacology ; Glucose - metabolism ; Insulin - pharmacology ; Insulin Resistance - physiology ; Membrane Potential, Mitochondrial - drug effects ; Mice ; Mitochondria - drug effects ; Mitochondria - enzymology ; Mitochondria - pathology ; Muscle Cells - drug effects ; Muscle Cells - enzymology ; Muscle Cells - pathology ; Muscle Fibers, Skeletal - drug effects ; Muscle Fibers, Skeletal - enzymology ; Muscle Fibers, Skeletal - pathology ; Muscle, Skeletal - pathology ; Oligomycins - pharmacology ; Palmitic Acid - pharmacology ; Phosphorylation - drug effects ; Proto-Oncogene Proteins c-akt - metabolism ; Rats ; Rats, Wistar ; Stearic Acids - pharmacology</subject><ispartof>Journal of cellular physiology, 2010-01, Vol.222 (1), p.187-194</ispartof><rights>Copyright © 2009 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3626-160ac13bb02fff725386f0c3ef3190ea4f72e3fb536f565a5ab829edf9f3cdb53</citedby><cites>FETCH-LOGICAL-c3626-160ac13bb02fff725386f0c3ef3190ea4f72e3fb536f565a5ab829edf9f3cdb53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjcp.21936$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcp.21936$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19780047$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hirabara, Sandro M.</creatorcontrib><creatorcontrib>Curi, Rui</creatorcontrib><creatorcontrib>Maechler, Pierre</creatorcontrib><title>Saturated fatty acid-induced insulin resistance is associated with mitochondrial dysfunction in skeletal muscle cells</title><title>Journal of cellular physiology</title><addtitle>J. Cell. Physiol</addtitle><description>Increased plasma levels of free fatty acids (FFA) occur in states of insulin resistance such as obesity and type 2 diabetes mellitus. These high levels of plasma FFA are proposed to play an important role for the development of insulin resistance but the mechanisms involved are still unclear. This study investigated the effects of saturated and unsaturated FFA on insulin sensitivity in parallel with mitochondrial function. C2C12 myotubes were treated for 24 h with 0.1 mM of saturated (palmitic and stearic) and unsaturated (oleic, linoleic, eicosapentaenoic, and docosahexaenoic) FFA. After this period, basal and insulin‐stimulated glucose metabolism and mitochondrial function were evaluated. Saturated palmitic and stearic acids decreased insulin‐induced glycogen synthesis, glucose oxidation, and lactate production. Basal glucose oxidation was also reduced. Palmitic and stearic acids impaired mitochondrial function as demonstrated by decrease of both mitochondrial hyperpolarization and ATP generation. These FFA also decreased Akt activation by insulin. As opposed to saturated FFA, unsaturated FFA did not impair glucose metabolism and mitochondrial function. Primary cultures of rat skeletal muscle cells exhibited similar responses to saturated FFA as compared to C2C12 cells. These results show that in muscle cells saturated FFA‐induced mitochondrial dysfunction associated with impaired insulin‐induced glucose metabolism. J. Cell. Physiol. 222:187–194, 2010. © 2009 Wiley‐Liss, Inc.</description><subject>Adenosine Triphosphate - biosynthesis</subject><subject>Animals</subject><subject>Cell Survival - drug effects</subject><subject>Cells, Cultured</subject><subject>Fatty Acids - pharmacology</subject><subject>Glucose - metabolism</subject><subject>Insulin - pharmacology</subject><subject>Insulin Resistance - physiology</subject><subject>Membrane Potential, Mitochondrial - drug effects</subject><subject>Mice</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - enzymology</subject><subject>Mitochondria - pathology</subject><subject>Muscle Cells - drug effects</subject><subject>Muscle Cells - enzymology</subject><subject>Muscle Cells - pathology</subject><subject>Muscle Fibers, Skeletal - drug effects</subject><subject>Muscle Fibers, Skeletal - enzymology</subject><subject>Muscle Fibers, Skeletal - pathology</subject><subject>Muscle, Skeletal - pathology</subject><subject>Oligomycins - pharmacology</subject><subject>Palmitic Acid - pharmacology</subject><subject>Phosphorylation - drug effects</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Stearic Acids - pharmacology</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtvEzEUhS1ERUNhwR9A3iEW0_ox9sRLFJUCitpIAbG0PJ5r1e08wlxbJf8etwmw6srS8XeOrj5C3nF2zhkTF3d-dy64kfoFWXBmmqrWSrwki_LHK6NqfkpeI94xxoyR8hU55aZZMlY3C5K3LuXZJehocCntqfOxq-LYZV-iOGLu40hnwIjJjR5oROoQJx-fOg8x3dIhpsnfTmM3R9fTbo8hjz7FaSx9ivfQQyr5kNH3QD30Pb4hJ8H1CG-P7xn58fny--pLtb65-rr6tK681EJXXDPnuWxbJkIIjVByqQPzEoLkhoGrSwYytErqoLRyyrVLYaALJkjflfiMfDjs7ubpVwZMdoj4eIEbYcpoG1lzobjQhfx4IP08Ic4Q7G6Og5v3ljP7KNkWyfZJcmHfH1dzO0D3nzxaLcDFAXiIPeyfX7LfVpu_k9WhUTTD738NN99b3chG2Z_XV3bNt2yzMVu7lH8AL7WYdg</recordid><startdate>201001</startdate><enddate>201001</enddate><creator>Hirabara, Sandro M.</creator><creator>Curi, Rui</creator><creator>Maechler, Pierre</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>201001</creationdate><title>Saturated fatty acid-induced insulin resistance is associated with mitochondrial dysfunction in skeletal muscle cells</title><author>Hirabara, Sandro M. ; 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Saturated palmitic and stearic acids decreased insulin‐induced glycogen synthesis, glucose oxidation, and lactate production. Basal glucose oxidation was also reduced. Palmitic and stearic acids impaired mitochondrial function as demonstrated by decrease of both mitochondrial hyperpolarization and ATP generation. These FFA also decreased Akt activation by insulin. As opposed to saturated FFA, unsaturated FFA did not impair glucose metabolism and mitochondrial function. Primary cultures of rat skeletal muscle cells exhibited similar responses to saturated FFA as compared to C2C12 cells. These results show that in muscle cells saturated FFA‐induced mitochondrial dysfunction associated with impaired insulin‐induced glucose metabolism. J. Cell. Physiol. 222:187–194, 2010. © 2009 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19780047</pmid><doi>10.1002/jcp.21936</doi><tpages>8</tpages></addata></record> |
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subjects | Adenosine Triphosphate - biosynthesis Animals Cell Survival - drug effects Cells, Cultured Fatty Acids - pharmacology Glucose - metabolism Insulin - pharmacology Insulin Resistance - physiology Membrane Potential, Mitochondrial - drug effects Mice Mitochondria - drug effects Mitochondria - enzymology Mitochondria - pathology Muscle Cells - drug effects Muscle Cells - enzymology Muscle Cells - pathology Muscle Fibers, Skeletal - drug effects Muscle Fibers, Skeletal - enzymology Muscle Fibers, Skeletal - pathology Muscle, Skeletal - pathology Oligomycins - pharmacology Palmitic Acid - pharmacology Phosphorylation - drug effects Proto-Oncogene Proteins c-akt - metabolism Rats Rats, Wistar Stearic Acids - pharmacology |
title | Saturated fatty acid-induced insulin resistance is associated with mitochondrial dysfunction in skeletal muscle cells |
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