A single prior bout of exercise protects against palmitate-induced insulin resistance despite an increase in total ceramide content
Ceramide accumulation has been implicated in the impairment of insulin-stimulated glucose transport in skeletal muscle following saturated fatty acid (FA) exposure. Importantly, a single bout of exercise can protect against acute lipid-induced insulin resistance. The mechanism by which exercise prot...
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creator | Thrush, A Brianne Harasim, Ewa Chabowski, Adrian Gulli, Roberto Stefanyk, Leslie Dyck, David J |
description | Ceramide accumulation has been implicated in the impairment of insulin-stimulated glucose transport in skeletal muscle following saturated fatty acid (FA) exposure. Importantly, a single bout of exercise can protect against acute lipid-induced insulin resistance. The mechanism by which exercise protects against lipid-induced insulin resistance is not completely known but may occur through a redirection of FA toward triacylglycerol (TAG) and away from ceramide and diacylglycerol (DAG). Therefore, in the current study, an in vitro preparation was used to examine whether a prior bout of exercise could confer protection against palmitate-induced insulin resistance and whether the pharmacological [50 μM fumonisin B(1) (FB1)] inhibition of ceramide synthesis in the presence of palmitate could mimic the protective effect of exercise. Soleus muscle of sedentary (SED), exercised (EX), and SED in the presence of FB1 (SED+FB1) were incubated with or without 2 mM palmitate for 4 h. This 2-mM palmitate exposure impaired insulin-stimulated glucose transport (-28%, P < 0.01) and significantly increased ceramide, DAG, and TAG accumulation in the SED group (P < 0.05). A single prior bout of exercise prevented the detrimental effects of palmitate on insulin signaling and caused a partial redistribution of FA toward TAG (P < 0.05). However, the net increase in ceramide content in response to palmitate exposure in the EX group was not different compared with SED, despite the maintenance of insulin sensitivity. The incubation of soleus from SED rats with FB1 (SED+FB1) prevented the detrimental effects of palmitate and caused a redirection of FA toward TAG accumulation (P < 0.05). Therefore, this research suggests that although inhibiting ceramide accumulation can prevent the detrimental effects of palmitate, a single prior bout of exercise appears to protect against palmitate-induced insulin resistance, which may be independent of changes in ceramide content. |
doi_str_mv | 10.1152/ajpregu.00091.2010 |
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Importantly, a single bout of exercise can protect against acute lipid-induced insulin resistance. The mechanism by which exercise protects against lipid-induced insulin resistance is not completely known but may occur through a redirection of FA toward triacylglycerol (TAG) and away from ceramide and diacylglycerol (DAG). Therefore, in the current study, an in vitro preparation was used to examine whether a prior bout of exercise could confer protection against palmitate-induced insulin resistance and whether the pharmacological [50 μM fumonisin B(1) (FB1)] inhibition of ceramide synthesis in the presence of palmitate could mimic the protective effect of exercise. Soleus muscle of sedentary (SED), exercised (EX), and SED in the presence of FB1 (SED+FB1) were incubated with or without 2 mM palmitate for 4 h. This 2-mM palmitate exposure impaired insulin-stimulated glucose transport (-28%, P < 0.01) and significantly increased ceramide, DAG, and TAG accumulation in the SED group (P < 0.05). A single prior bout of exercise prevented the detrimental effects of palmitate on insulin signaling and caused a partial redistribution of FA toward TAG (P < 0.05). However, the net increase in ceramide content in response to palmitate exposure in the EX group was not different compared with SED, despite the maintenance of insulin sensitivity. The incubation of soleus from SED rats with FB1 (SED+FB1) prevented the detrimental effects of palmitate and caused a redirection of FA toward TAG accumulation (P < 0.05). Therefore, this research suggests that although inhibiting ceramide accumulation can prevent the detrimental effects of palmitate, a single prior bout of exercise appears to protect against palmitate-induced insulin resistance, which may be independent of changes in ceramide content.</description><identifier>ISSN: 0363-6119</identifier><identifier>EISSN: 1522-1490</identifier><identifier>DOI: 10.1152/ajpregu.00091.2010</identifier><identifier>PMID: 21325642</identifier><identifier>CODEN: AJPRDO</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Ceramides - metabolism ; Diglycerides - metabolism ; Energy Metabolism - drug effects ; Enzyme Inhibitors - pharmacology ; Exercise ; Fatty acids ; Female ; Fumonisins - pharmacology ; Glucose ; Glucose - metabolism ; In Vitro Techniques ; Insulin - metabolism ; Insulin Resistance ; Muscle Contraction ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - metabolism ; Muscle, Skeletal - physiopathology ; Oxidation-Reduction ; Oxidoreductases - antagonists & inhibitors ; Oxidoreductases - metabolism ; Palmitic Acid - metabolism ; Physical Exertion ; Rats ; Rats, Sprague-Dawley ; Rodents ; Signal transduction ; Studies ; Time Factors ; Triglycerides - metabolism ; Up-Regulation</subject><ispartof>American journal of physiology. Regulatory, integrative and comparative physiology, 2011-05, Vol.300 (5), p.R1200-R1208</ispartof><rights>Copyright American Physiological Society May 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c329t-f22ca5993151e8cb12fbd04a51414ac7a73ddb7d69cbc6a4853b3aef43197f043</citedby><cites>FETCH-LOGICAL-c329t-f22ca5993151e8cb12fbd04a51414ac7a73ddb7d69cbc6a4853b3aef43197f043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3037,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21325642$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thrush, A Brianne</creatorcontrib><creatorcontrib>Harasim, Ewa</creatorcontrib><creatorcontrib>Chabowski, Adrian</creatorcontrib><creatorcontrib>Gulli, Roberto</creatorcontrib><creatorcontrib>Stefanyk, Leslie</creatorcontrib><creatorcontrib>Dyck, David J</creatorcontrib><title>A single prior bout of exercise protects against palmitate-induced insulin resistance despite an increase in total ceramide content</title><title>American journal of physiology. Regulatory, integrative and comparative physiology</title><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><description>Ceramide accumulation has been implicated in the impairment of insulin-stimulated glucose transport in skeletal muscle following saturated fatty acid (FA) exposure. Importantly, a single bout of exercise can protect against acute lipid-induced insulin resistance. The mechanism by which exercise protects against lipid-induced insulin resistance is not completely known but may occur through a redirection of FA toward triacylglycerol (TAG) and away from ceramide and diacylglycerol (DAG). Therefore, in the current study, an in vitro preparation was used to examine whether a prior bout of exercise could confer protection against palmitate-induced insulin resistance and whether the pharmacological [50 μM fumonisin B(1) (FB1)] inhibition of ceramide synthesis in the presence of palmitate could mimic the protective effect of exercise. Soleus muscle of sedentary (SED), exercised (EX), and SED in the presence of FB1 (SED+FB1) were incubated with or without 2 mM palmitate for 4 h. This 2-mM palmitate exposure impaired insulin-stimulated glucose transport (-28%, P < 0.01) and significantly increased ceramide, DAG, and TAG accumulation in the SED group (P < 0.05). A single prior bout of exercise prevented the detrimental effects of palmitate on insulin signaling and caused a partial redistribution of FA toward TAG (P < 0.05). However, the net increase in ceramide content in response to palmitate exposure in the EX group was not different compared with SED, despite the maintenance of insulin sensitivity. The incubation of soleus from SED rats with FB1 (SED+FB1) prevented the detrimental effects of palmitate and caused a redirection of FA toward TAG accumulation (P < 0.05). Therefore, this research suggests that although inhibiting ceramide accumulation can prevent the detrimental effects of palmitate, a single prior bout of exercise appears to protect against palmitate-induced insulin resistance, which may be independent of changes in ceramide content.</description><subject>Animals</subject><subject>Ceramides - metabolism</subject><subject>Diglycerides - metabolism</subject><subject>Energy Metabolism - drug effects</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Exercise</subject><subject>Fatty acids</subject><subject>Female</subject><subject>Fumonisins - pharmacology</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>In Vitro Techniques</subject><subject>Insulin - metabolism</subject><subject>Insulin Resistance</subject><subject>Muscle Contraction</subject><subject>Muscle, Skeletal - drug effects</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Muscle, Skeletal - physiopathology</subject><subject>Oxidation-Reduction</subject><subject>Oxidoreductases - antagonists & inhibitors</subject><subject>Oxidoreductases - metabolism</subject><subject>Palmitic Acid - metabolism</subject><subject>Physical Exertion</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rodents</subject><subject>Signal transduction</subject><subject>Studies</subject><subject>Time Factors</subject><subject>Triglycerides - metabolism</subject><subject>Up-Regulation</subject><issn>0363-6119</issn><issn>1522-1490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1v1DAQhi0EotuPP8ABWVw4ZeuxnWR9rKpCkSpxgXM0sScrrxJ7sR0JzvzxeunCgZOlmWdeeeZh7B2ILUArb_FwTLRft0IIA1spQLxim9qQDWgjXrONUJ1qOgBzwS5zPlROK63esgsJSradlhv2-45nH_Yz8WPyMfExroXHidNPStbnUzkWsiVz3KMPufAjzosvWKjxwa2WHK_ldfaBJ8o-FwyWuKN89IU4htq1ibAmVaLEgjO3lHDxjriNoVAo1-zNhHOmm_N7xb5_evh2_9g8ff385f7uqbFKmtJMUlpsjVHQAu3sCHIandDYggaNtsdeOTf2rjN2tB3qXatGhTRpBaaf6upX7ONLbt3px0q5DIvPluYZA8U1D7tOm9bsdFfJD_-Rh7imUD9Xob7vOw2mQvIFsinmnGga6gkXTL8GEMNJ0HAWNPwRNJwE1aH35-R1XMj9G_lrRD0DwXaQPw</recordid><startdate>201105</startdate><enddate>201105</enddate><creator>Thrush, A Brianne</creator><creator>Harasim, Ewa</creator><creator>Chabowski, Adrian</creator><creator>Gulli, Roberto</creator><creator>Stefanyk, Leslie</creator><creator>Dyck, David J</creator><general>American Physiological Society</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>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201105</creationdate><title>A single prior bout of exercise protects against palmitate-induced insulin resistance despite an increase in total ceramide content</title><author>Thrush, A Brianne ; Harasim, Ewa ; Chabowski, Adrian ; Gulli, Roberto ; Stefanyk, Leslie ; Dyck, David J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c329t-f22ca5993151e8cb12fbd04a51414ac7a73ddb7d69cbc6a4853b3aef43197f043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Ceramides - metabolism</topic><topic>Diglycerides - metabolism</topic><topic>Energy Metabolism - drug effects</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Exercise</topic><topic>Fatty acids</topic><topic>Female</topic><topic>Fumonisins - pharmacology</topic><topic>Glucose</topic><topic>Glucose - metabolism</topic><topic>In Vitro Techniques</topic><topic>Insulin - metabolism</topic><topic>Insulin Resistance</topic><topic>Muscle Contraction</topic><topic>Muscle, Skeletal - drug effects</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Muscle, Skeletal - physiopathology</topic><topic>Oxidation-Reduction</topic><topic>Oxidoreductases - antagonists & inhibitors</topic><topic>Oxidoreductases - metabolism</topic><topic>Palmitic Acid - metabolism</topic><topic>Physical Exertion</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Rodents</topic><topic>Signal transduction</topic><topic>Studies</topic><topic>Time Factors</topic><topic>Triglycerides - metabolism</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thrush, A Brianne</creatorcontrib><creatorcontrib>Harasim, Ewa</creatorcontrib><creatorcontrib>Chabowski, Adrian</creatorcontrib><creatorcontrib>Gulli, Roberto</creatorcontrib><creatorcontrib>Stefanyk, Leslie</creatorcontrib><creatorcontrib>Dyck, David J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thrush, A Brianne</au><au>Harasim, Ewa</au><au>Chabowski, Adrian</au><au>Gulli, Roberto</au><au>Stefanyk, Leslie</au><au>Dyck, David J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A single prior bout of exercise protects against palmitate-induced insulin resistance despite an increase in total ceramide content</atitle><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><date>2011-05</date><risdate>2011</risdate><volume>300</volume><issue>5</issue><spage>R1200</spage><epage>R1208</epage><pages>R1200-R1208</pages><issn>0363-6119</issn><eissn>1522-1490</eissn><coden>AJPRDO</coden><abstract>Ceramide accumulation has been implicated in the impairment of insulin-stimulated glucose transport in skeletal muscle following saturated fatty acid (FA) exposure. Importantly, a single bout of exercise can protect against acute lipid-induced insulin resistance. The mechanism by which exercise protects against lipid-induced insulin resistance is not completely known but may occur through a redirection of FA toward triacylglycerol (TAG) and away from ceramide and diacylglycerol (DAG). Therefore, in the current study, an in vitro preparation was used to examine whether a prior bout of exercise could confer protection against palmitate-induced insulin resistance and whether the pharmacological [50 μM fumonisin B(1) (FB1)] inhibition of ceramide synthesis in the presence of palmitate could mimic the protective effect of exercise. Soleus muscle of sedentary (SED), exercised (EX), and SED in the presence of FB1 (SED+FB1) were incubated with or without 2 mM palmitate for 4 h. This 2-mM palmitate exposure impaired insulin-stimulated glucose transport (-28%, P < 0.01) and significantly increased ceramide, DAG, and TAG accumulation in the SED group (P < 0.05). A single prior bout of exercise prevented the detrimental effects of palmitate on insulin signaling and caused a partial redistribution of FA toward TAG (P < 0.05). However, the net increase in ceramide content in response to palmitate exposure in the EX group was not different compared with SED, despite the maintenance of insulin sensitivity. The incubation of soleus from SED rats with FB1 (SED+FB1) prevented the detrimental effects of palmitate and caused a redirection of FA toward TAG accumulation (P < 0.05). Therefore, this research suggests that although inhibiting ceramide accumulation can prevent the detrimental effects of palmitate, a single prior bout of exercise appears to protect against palmitate-induced insulin resistance, which may be independent of changes in ceramide content.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>21325642</pmid><doi>10.1152/ajpregu.00091.2010</doi></addata></record> |
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subjects | Animals Ceramides - metabolism Diglycerides - metabolism Energy Metabolism - drug effects Enzyme Inhibitors - pharmacology Exercise Fatty acids Female Fumonisins - pharmacology Glucose Glucose - metabolism In Vitro Techniques Insulin - metabolism Insulin Resistance Muscle Contraction Muscle, Skeletal - drug effects Muscle, Skeletal - metabolism Muscle, Skeletal - physiopathology Oxidation-Reduction Oxidoreductases - antagonists & inhibitors Oxidoreductases - metabolism Palmitic Acid - metabolism Physical Exertion Rats Rats, Sprague-Dawley Rodents Signal transduction Studies Time Factors Triglycerides - metabolism Up-Regulation |
title | A single prior bout of exercise protects against palmitate-induced insulin resistance despite an increase in total ceramide content |
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