Curcumin treatment enhances the effect of exercise on mitochondrial biogenesis in skeletal muscle by increasing cAMP levels

Abstract Background In response to physiologic stressors, skeletal muscle has the potential to elicit wide variety of adaptive responses, such as biogenesis of mitochondria and clearance of damaged mitochondria to promote healthy muscle. The polyphenol curcumin, derived from the rhizome Curcuma long...

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Veröffentlicht in:Metabolism, clinical and experimental clinical and experimental, 2015-10, Vol.64 (10), p.1334-1347
Hauptverfasser: Ray Hamidie, Ronald D, Yamada, Tatsuya, Ishizawa, Rie, Saito, Yoko, Masuda, Kazumi
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container_end_page 1347
container_issue 10
container_start_page 1334
container_title Metabolism, clinical and experimental
container_volume 64
creator Ray Hamidie, Ronald D
Yamada, Tatsuya
Ishizawa, Rie
Saito, Yoko
Masuda, Kazumi
description Abstract Background In response to physiologic stressors, skeletal muscle has the potential to elicit wide variety of adaptive responses, such as biogenesis of mitochondria and clearance of damaged mitochondria to promote healthy muscle. The polyphenol curcumin, derived from the rhizome Curcuma longa L ., is a natural antioxidant that exhibits various pharmacological activities and therapeutic properties. However, the effect of curcumin on the regulation of mitochondrial biogenesis in skeletal muscle remains unknown. The present study aimed to examine the effects of combination of endurance training (eTR) and curcumin treatment on the expression of AMPK, SIRT1, PGC-1α, and OXPHOS subunits, mitochondrial DNA copy number, and CS activity in rat skeletal muscle. Furthermore, the present study also examined the effect of exercise and curcumin treatment on the levels of cAMP and downstream targets of PKA including phosphorylated CREB and LKB-1. Methods Ten-week-old male Wistar rats were randomly divided into non-eTR and eTR groups. Low doses (50 mg/kg-BW/day) or high doses (100 mg/kg-BW/day) of curcumin dissolved in dimethyl sulfoxide (DMSO) were injected intraperitoneally in all animals for 28 days to investigate the effect of curcumin alone and the combined effect of curcumin with eTR. Western blotting (WB) and immunoprecipitation (IP) were performed to detect the presence of proteins. Results Our results demonstrated that combination of curcumin treatment and eTR increased the expression of COX-IV, OXPHOS subunits, mitochondrial DNA copy number and CS activity in the gastrocnemius (Gas) and soleus (Sol) muscles. In addition, this combination increased AMPK phosphorylation, NAD+ /NADH ratio, SIRT1 expression, and PGC-1α deacetylation. Furthermore, curcumin treatment as well as exercise also increased levels of cAMP and downstream target of PKA including phosphorylation CREB and LKB-1 which are involved in the regulation of mitochondrial biogenesis. Conclusion Taken together, these results suggest that the combination of curcumin treatment and eTR has the potential to accelerate mitochondrial biogenesis in skeletal muscle by increasing cAMP levels.
doi_str_mv 10.1016/j.metabol.2015.07.010
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The polyphenol curcumin, derived from the rhizome Curcuma longa L ., is a natural antioxidant that exhibits various pharmacological activities and therapeutic properties. However, the effect of curcumin on the regulation of mitochondrial biogenesis in skeletal muscle remains unknown. The present study aimed to examine the effects of combination of endurance training (eTR) and curcumin treatment on the expression of AMPK, SIRT1, PGC-1α, and OXPHOS subunits, mitochondrial DNA copy number, and CS activity in rat skeletal muscle. Furthermore, the present study also examined the effect of exercise and curcumin treatment on the levels of cAMP and downstream targets of PKA including phosphorylated CREB and LKB-1. Methods Ten-week-old male Wistar rats were randomly divided into non-eTR and eTR groups. Low doses (50 mg/kg-BW/day) or high doses (100 mg/kg-BW/day) of curcumin dissolved in dimethyl sulfoxide (DMSO) were injected intraperitoneally in all animals for 28 days to investigate the effect of curcumin alone and the combined effect of curcumin with eTR. Western blotting (WB) and immunoprecipitation (IP) were performed to detect the presence of proteins. Results Our results demonstrated that combination of curcumin treatment and eTR increased the expression of COX-IV, OXPHOS subunits, mitochondrial DNA copy number and CS activity in the gastrocnemius (Gas) and soleus (Sol) muscles. In addition, this combination increased AMPK phosphorylation, NAD+ /NADH ratio, SIRT1 expression, and PGC-1α deacetylation. Furthermore, curcumin treatment as well as exercise also increased levels of cAMP and downstream target of PKA including phosphorylation CREB and LKB-1 which are involved in the regulation of mitochondrial biogenesis. Conclusion Taken together, these results suggest that the combination of curcumin treatment and eTR has the potential to accelerate mitochondrial biogenesis in skeletal muscle by increasing cAMP levels.</description><identifier>ISSN: 0026-0495</identifier><identifier>EISSN: 1532-8600</identifier><identifier>DOI: 10.1016/j.metabol.2015.07.010</identifier><identifier>PMID: 26278015</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Body Weight - drug effects ; cAMP ; Curcumin - pharmacology ; Cyclic AMP - metabolism ; Electron Transport Complex IV - metabolism ; Endocrinology &amp; Metabolism ; Endurance training ; Male ; Mitochondria ; Mitochondria, Muscle - drug effects ; Mitochondria, Muscle - physiology ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - metabolism ; Organelle Biogenesis ; Oxidative Phosphorylation - drug effects ; Physical Conditioning, Animal - physiology ; Physical Endurance - drug effects ; Physical Endurance - genetics ; Polyphenol ; Rats ; Rats, Wistar ; Skeletal muscle ; Up-Regulation - drug effects</subject><ispartof>Metabolism, clinical and experimental, 2015-10, Vol.64 (10), p.1334-1347</ispartof><rights>Elsevier Inc.</rights><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. 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The polyphenol curcumin, derived from the rhizome Curcuma longa L ., is a natural antioxidant that exhibits various pharmacological activities and therapeutic properties. However, the effect of curcumin on the regulation of mitochondrial biogenesis in skeletal muscle remains unknown. The present study aimed to examine the effects of combination of endurance training (eTR) and curcumin treatment on the expression of AMPK, SIRT1, PGC-1α, and OXPHOS subunits, mitochondrial DNA copy number, and CS activity in rat skeletal muscle. Furthermore, the present study also examined the effect of exercise and curcumin treatment on the levels of cAMP and downstream targets of PKA including phosphorylated CREB and LKB-1. Methods Ten-week-old male Wistar rats were randomly divided into non-eTR and eTR groups. Low doses (50 mg/kg-BW/day) or high doses (100 mg/kg-BW/day) of curcumin dissolved in dimethyl sulfoxide (DMSO) were injected intraperitoneally in all animals for 28 days to investigate the effect of curcumin alone and the combined effect of curcumin with eTR. Western blotting (WB) and immunoprecipitation (IP) were performed to detect the presence of proteins. Results Our results demonstrated that combination of curcumin treatment and eTR increased the expression of COX-IV, OXPHOS subunits, mitochondrial DNA copy number and CS activity in the gastrocnemius (Gas) and soleus (Sol) muscles. In addition, this combination increased AMPK phosphorylation, NAD+ /NADH ratio, SIRT1 expression, and PGC-1α deacetylation. Furthermore, curcumin treatment as well as exercise also increased levels of cAMP and downstream target of PKA including phosphorylation CREB and LKB-1 which are involved in the regulation of mitochondrial biogenesis. Conclusion Taken together, these results suggest that the combination of curcumin treatment and eTR has the potential to accelerate mitochondrial biogenesis in skeletal muscle by increasing cAMP levels.</description><subject>Animals</subject><subject>Body Weight - drug effects</subject><subject>cAMP</subject><subject>Curcumin - pharmacology</subject><subject>Cyclic AMP - metabolism</subject><subject>Electron Transport Complex IV - metabolism</subject><subject>Endocrinology &amp; Metabolism</subject><subject>Endurance training</subject><subject>Male</subject><subject>Mitochondria</subject><subject>Mitochondria, Muscle - drug effects</subject><subject>Mitochondria, Muscle - physiology</subject><subject>Muscle, Skeletal - drug effects</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Organelle Biogenesis</subject><subject>Oxidative Phosphorylation - drug effects</subject><subject>Physical Conditioning, Animal - physiology</subject><subject>Physical Endurance - drug effects</subject><subject>Physical Endurance - genetics</subject><subject>Polyphenol</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Skeletal muscle</subject><subject>Up-Regulation - drug effects</subject><issn>0026-0495</issn><issn>1532-8600</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU-PFCEQxYnRuOPqR9Bw9NJt0d1A90WzmfgvWaOJeiY0XewwS8MK3RsnfnmZzOjBiydS8N4r6leEPGdQM2Di1b6ecdFj9HUDjNcga2DwgGwYb5uqFwAPyQagERV0A78gT3LeA4CUvXhMLhrRyL7YNuTXdk1mnV2gS0K9zBgWimGng8FMlx1StBbNQqOl-BOTcRlpDHR2SzS7GKbktKejizcYMLtMS1C-RV--5um8ZuORjodya0p6duGGmqtPX6jHe_T5KXlktc_47Hxeku_v3n7bfqiuP7__uL26rgznYqnsILtGjH3bSsah07rtre16NvWWs2Hgwzh0BkrVCC54eRn6QRjLrB6tmDreXpKXp9y7FH-smBc1u2zQex0wrlkxyRpZyLSySPlJalLMOaFVd8nNOh0UA3XkrvbqzF0duSuQqnAvvhfnFus44_TX9Qd0Ebw5CcrceO8wqWwcFsqTS4WvmqL7b4vX_yQY74Iz2t_iAfM-rikUioqp3ChQX4_LP-6-MAM2ALS_AYfZrM0</recordid><startdate>20151001</startdate><enddate>20151001</enddate><creator>Ray Hamidie, Ronald D</creator><creator>Yamada, Tatsuya</creator><creator>Ishizawa, Rie</creator><creator>Saito, Yoko</creator><creator>Masuda, Kazumi</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>20151001</creationdate><title>Curcumin treatment enhances the effect of exercise on mitochondrial biogenesis in skeletal muscle by increasing cAMP levels</title><author>Ray Hamidie, Ronald D ; Yamada, Tatsuya ; Ishizawa, Rie ; Saito, Yoko ; Masuda, Kazumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c556t-f97426b83371504aa38ff481d8f519959b94c0d8f26565f489896cf1fabf6d453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Body Weight - drug effects</topic><topic>cAMP</topic><topic>Curcumin - pharmacology</topic><topic>Cyclic AMP - metabolism</topic><topic>Electron Transport Complex IV - metabolism</topic><topic>Endocrinology &amp; Metabolism</topic><topic>Endurance training</topic><topic>Male</topic><topic>Mitochondria</topic><topic>Mitochondria, Muscle - drug effects</topic><topic>Mitochondria, Muscle - physiology</topic><topic>Muscle, Skeletal - drug effects</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Organelle Biogenesis</topic><topic>Oxidative Phosphorylation - drug effects</topic><topic>Physical Conditioning, Animal - physiology</topic><topic>Physical Endurance - drug effects</topic><topic>Physical Endurance - genetics</topic><topic>Polyphenol</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Skeletal muscle</topic><topic>Up-Regulation - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ray Hamidie, Ronald D</creatorcontrib><creatorcontrib>Yamada, Tatsuya</creatorcontrib><creatorcontrib>Ishizawa, Rie</creatorcontrib><creatorcontrib>Saito, Yoko</creatorcontrib><creatorcontrib>Masuda, Kazumi</creatorcontrib><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>Metabolism, clinical and experimental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ray Hamidie, Ronald D</au><au>Yamada, Tatsuya</au><au>Ishizawa, Rie</au><au>Saito, Yoko</au><au>Masuda, Kazumi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Curcumin treatment enhances the effect of exercise on mitochondrial biogenesis in skeletal muscle by increasing cAMP levels</atitle><jtitle>Metabolism, clinical and experimental</jtitle><addtitle>Metabolism</addtitle><date>2015-10-01</date><risdate>2015</risdate><volume>64</volume><issue>10</issue><spage>1334</spage><epage>1347</epage><pages>1334-1347</pages><issn>0026-0495</issn><eissn>1532-8600</eissn><abstract>Abstract Background In response to physiologic stressors, skeletal muscle has the potential to elicit wide variety of adaptive responses, such as biogenesis of mitochondria and clearance of damaged mitochondria to promote healthy muscle. The polyphenol curcumin, derived from the rhizome Curcuma longa L ., is a natural antioxidant that exhibits various pharmacological activities and therapeutic properties. However, the effect of curcumin on the regulation of mitochondrial biogenesis in skeletal muscle remains unknown. The present study aimed to examine the effects of combination of endurance training (eTR) and curcumin treatment on the expression of AMPK, SIRT1, PGC-1α, and OXPHOS subunits, mitochondrial DNA copy number, and CS activity in rat skeletal muscle. Furthermore, the present study also examined the effect of exercise and curcumin treatment on the levels of cAMP and downstream targets of PKA including phosphorylated CREB and LKB-1. Methods Ten-week-old male Wistar rats were randomly divided into non-eTR and eTR groups. Low doses (50 mg/kg-BW/day) or high doses (100 mg/kg-BW/day) of curcumin dissolved in dimethyl sulfoxide (DMSO) were injected intraperitoneally in all animals for 28 days to investigate the effect of curcumin alone and the combined effect of curcumin with eTR. Western blotting (WB) and immunoprecipitation (IP) were performed to detect the presence of proteins. Results Our results demonstrated that combination of curcumin treatment and eTR increased the expression of COX-IV, OXPHOS subunits, mitochondrial DNA copy number and CS activity in the gastrocnemius (Gas) and soleus (Sol) muscles. In addition, this combination increased AMPK phosphorylation, NAD+ /NADH ratio, SIRT1 expression, and PGC-1α deacetylation. Furthermore, curcumin treatment as well as exercise also increased levels of cAMP and downstream target of PKA including phosphorylation CREB and LKB-1 which are involved in the regulation of mitochondrial biogenesis. Conclusion Taken together, these results suggest that the combination of curcumin treatment and eTR has the potential to accelerate mitochondrial biogenesis in skeletal muscle by increasing cAMP levels.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26278015</pmid><doi>10.1016/j.metabol.2015.07.010</doi><tpages>14</tpages></addata></record>
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subjects Animals
Body Weight - drug effects
cAMP
Curcumin - pharmacology
Cyclic AMP - metabolism
Electron Transport Complex IV - metabolism
Endocrinology & Metabolism
Endurance training
Male
Mitochondria
Mitochondria, Muscle - drug effects
Mitochondria, Muscle - physiology
Muscle, Skeletal - drug effects
Muscle, Skeletal - metabolism
Organelle Biogenesis
Oxidative Phosphorylation - drug effects
Physical Conditioning, Animal - physiology
Physical Endurance - drug effects
Physical Endurance - genetics
Polyphenol
Rats
Rats, Wistar
Skeletal muscle
Up-Regulation - drug effects
title Curcumin treatment enhances the effect of exercise on mitochondrial biogenesis in skeletal muscle by increasing cAMP levels
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