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The PPARα Agonist Fenofibrate Improves the Musculoskeletal Effects of Exercise in Ovariectomized Rats
The musculoskeletal effects of exercise are attenuated by estrogen deficiency. The peroxisome proliferator-activated receptor-α agonist fenofibrate exerts beneficial effects in bone and muscle. We therefore examined whether fenofibrate could enhance the musculoskeletal training response during estro...
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Published in: | Endocrinology (Philadelphia) 2016-10, Vol.157 (10), p.3924-3934 |
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description | The musculoskeletal effects of exercise are attenuated by estrogen deficiency. The peroxisome proliferator-activated receptor-α agonist fenofibrate exerts beneficial effects in bone and muscle. We therefore examined whether fenofibrate could enhance the musculoskeletal training response during estrogen deficiency. We investigated the combined effects of 8 weeks of fenofibrate and jumping exercise in ovariectomized (OVX) Sprague Dawley rats. Female rats were allocated to a sham-operated group and four OVX groups; fenofibrate (OVX-Fen), exercise (OVX-Ex), combined fenofibrate and exercise (OVX-FenEx), and a control group (OVX-Ctr) (n = 12/group). Fenofibrate (90 mg/kg/d) or methylcellulose was given by gavage. The combination of exercise and fenofibrate resulted in enhanced femoral bone mineral density (BMD) and improved bone microarchitecture compared with fenofibrate alone as well as increased trabecular BMD compared with OVX-Ctr. These effects were not seen in the OVX-Ex group. Femoral BMD was normalized in both exercise groups relative to sham and increased more in all intervention groups compared with OVX-Ctr. A higher plasma level of the bone formation marker type 1 collagen amino propeptide was observed in the OVX-Fen and OVX-FenEx groups compared with controls. Lean mass and soleus muscle weight were higher in the OVX-FenEx group than in the OVX-Ctr group, which coincided with lower mRNA levels of Atrogin1. These results suggest that peroxisome proliferator-activated receptor-α activation improves the musculoskeletal effects of exercise during estrogen deficiency. |
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The peroxisome proliferator-activated receptor-α agonist fenofibrate exerts beneficial effects in bone and muscle. We therefore examined whether fenofibrate could enhance the musculoskeletal training response during estrogen deficiency. We investigated the combined effects of 8 weeks of fenofibrate and jumping exercise in ovariectomized (OVX) Sprague Dawley rats. Female rats were allocated to a sham-operated group and four OVX groups; fenofibrate (OVX-Fen), exercise (OVX-Ex), combined fenofibrate and exercise (OVX-FenEx), and a control group (OVX-Ctr) (n = 12/group). Fenofibrate (90 mg/kg/d) or methylcellulose was given by gavage. The combination of exercise and fenofibrate resulted in enhanced femoral bone mineral density (BMD) and improved bone microarchitecture compared with fenofibrate alone as well as increased trabecular BMD compared with OVX-Ctr. These effects were not seen in the OVX-Ex group. Femoral BMD was normalized in both exercise groups relative to sham and increased more in all intervention groups compared with OVX-Ctr. A higher plasma level of the bone formation marker type 1 collagen amino propeptide was observed in the OVX-Fen and OVX-FenEx groups compared with controls. Lean mass and soleus muscle weight were higher in the OVX-FenEx group than in the OVX-Ctr group, which coincided with lower mRNA levels of Atrogin1. These results suggest that peroxisome proliferator-activated receptor-α activation improves the musculoskeletal effects of exercise during estrogen deficiency.</description><identifier>ISSN: 0013-7227</identifier><identifier>ISSN: 1945-7170</identifier><identifier>EISSN: 1945-7170</identifier><identifier>DOI: 10.1210/en.2016-1114</identifier><identifier>PMID: 27526032</identifier><language>eng</language><publisher>United States: Endocrine Society</publisher><subject>Agonists ; Animals ; Body Composition - drug effects ; Bone and Bones - drug effects ; Bone and Bones - metabolism ; Bone Density - drug effects ; Bone growth ; Bone mass ; Bone mineral density ; Cancellous bone ; Drug Evaluation, Preclinical ; Estrogens ; Estrogens - deficiency ; Female ; Femur ; Fenofibrate ; Fenofibrate - pharmacology ; Fenofibrate - therapeutic use ; Humans ; Jumping ; Methylcellulose ; mRNA ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - metabolism ; Muscles ; Osteogenesis ; Osteogenesis - drug effects ; Ovariectomy ; Peroxisome proliferator-activated receptors ; Physical Conditioning, Animal ; PPAR alpha - agonists ; Random Allocation ; Rats, Sprague-Dawley ; Receptors ; Soleus muscle ; Tibia - diagnostic imaging ; Tibia - drug effects ; X-Ray Microtomography</subject><ispartof>Endocrinology (Philadelphia), 2016-10, Vol.157 (10), p.3924-3934</ispartof><rights>Copyright © 2016 by the Endocrine Society</rights><rights>Copyright © 2016 by the Endocrine Society 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-c53e6499a7bb9b2baf760d5bdaa827ceeb6050080e0e8f2a5e4b5d31952b7a833</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27526032$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-126946$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Mosti, Mats Peder</creatorcontrib><creatorcontrib>Ericsson, Madelene</creatorcontrib><creatorcontrib>Erben, Reinhold G</creatorcontrib><creatorcontrib>Schüler, Christiane</creatorcontrib><creatorcontrib>Syversen, Unni</creatorcontrib><creatorcontrib>Stunes, Astrid Kamilla</creatorcontrib><title>The PPARα Agonist Fenofibrate Improves the Musculoskeletal Effects of Exercise in Ovariectomized Rats</title><title>Endocrinology (Philadelphia)</title><addtitle>Endocrinology</addtitle><description>The musculoskeletal effects of exercise are attenuated by estrogen deficiency. The peroxisome proliferator-activated receptor-α agonist fenofibrate exerts beneficial effects in bone and muscle. We therefore examined whether fenofibrate could enhance the musculoskeletal training response during estrogen deficiency. We investigated the combined effects of 8 weeks of fenofibrate and jumping exercise in ovariectomized (OVX) Sprague Dawley rats. Female rats were allocated to a sham-operated group and four OVX groups; fenofibrate (OVX-Fen), exercise (OVX-Ex), combined fenofibrate and exercise (OVX-FenEx), and a control group (OVX-Ctr) (n = 12/group). Fenofibrate (90 mg/kg/d) or methylcellulose was given by gavage. The combination of exercise and fenofibrate resulted in enhanced femoral bone mineral density (BMD) and improved bone microarchitecture compared with fenofibrate alone as well as increased trabecular BMD compared with OVX-Ctr. These effects were not seen in the OVX-Ex group. Femoral BMD was normalized in both exercise groups relative to sham and increased more in all intervention groups compared with OVX-Ctr. A higher plasma level of the bone formation marker type 1 collagen amino propeptide was observed in the OVX-Fen and OVX-FenEx groups compared with controls. Lean mass and soleus muscle weight were higher in the OVX-FenEx group than in the OVX-Ctr group, which coincided with lower mRNA levels of Atrogin1. These results suggest that peroxisome proliferator-activated receptor-α activation improves the musculoskeletal effects of exercise during estrogen deficiency.</description><subject>Agonists</subject><subject>Animals</subject><subject>Body Composition - drug effects</subject><subject>Bone and Bones - drug effects</subject><subject>Bone and Bones - metabolism</subject><subject>Bone Density - drug effects</subject><subject>Bone growth</subject><subject>Bone mass</subject><subject>Bone mineral density</subject><subject>Cancellous bone</subject><subject>Drug Evaluation, Preclinical</subject><subject>Estrogens</subject><subject>Estrogens - deficiency</subject><subject>Female</subject><subject>Femur</subject><subject>Fenofibrate</subject><subject>Fenofibrate - pharmacology</subject><subject>Fenofibrate - therapeutic use</subject><subject>Humans</subject><subject>Jumping</subject><subject>Methylcellulose</subject><subject>mRNA</subject><subject>Muscle, Skeletal - drug effects</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Muscles</subject><subject>Osteogenesis</subject><subject>Osteogenesis - drug effects</subject><subject>Ovariectomy</subject><subject>Peroxisome proliferator-activated receptors</subject><subject>Physical Conditioning, Animal</subject><subject>PPAR alpha - agonists</subject><subject>Random Allocation</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors</subject><subject>Soleus muscle</subject><subject>Tibia - diagnostic imaging</subject><subject>Tibia - drug effects</subject><subject>X-Ray Microtomography</subject><issn>0013-7227</issn><issn>1945-7170</issn><issn>1945-7170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp10ctu1DAUBmALgegwsGONLLGABSm-xHGyHJUpVCpqVRW2lp0cF5fETu24XN6KF-GZyChDkRCsLMuffp3jH6GnlBxSRslr8IeM0KqglJb30Io2pSgkleQ-WhFCeSEZkwfoUUrX87UsS_4QHTApWEU4WyF7-Qnw-fnm4ucPvLkK3qUJH4MP1pmoJ8AnwxjDLSQ8ze59Tm3uQ_oMPUy6x1troZ0SDhZvv0JsXQLsPD671dHND2Fw36HDF3pKj9EDq_sET_bnGn043l4evStOz96eHG1Oi7aUdCpawaEqm0ZLYxrDjLayIp0wndY1ky2AqYggpCZAoLZMCyiN6DhtBDNS15yvUbHkpi8wZqPG6AYdv6mgnXrjPm5UiFcqD1lRVjVlNfuXi5-3vMmQJjW41ELfaw8hJ0VrLnjdULGjz_-i1yFHP2-jOOWkYrKZP3eNXi2qjSGlCPZuBErUri8FXu36Uru-Zv5sH5rNAN0d_l3QDF4sIOTxf1HFPoovEnwX2ug8jBFS-jPlPwf4BZLwrg4</recordid><startdate>20161001</startdate><enddate>20161001</enddate><creator>Mosti, Mats Peder</creator><creator>Ericsson, Madelene</creator><creator>Erben, Reinhold G</creator><creator>Schüler, Christiane</creator><creator>Syversen, Unni</creator><creator>Stunes, Astrid Kamilla</creator><general>Endocrine Society</general><general>Oxford University Press</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>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D93</scope></search><sort><creationdate>20161001</creationdate><title>The PPARα Agonist Fenofibrate Improves the Musculoskeletal Effects of Exercise in Ovariectomized Rats</title><author>Mosti, Mats Peder ; 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The peroxisome proliferator-activated receptor-α agonist fenofibrate exerts beneficial effects in bone and muscle. We therefore examined whether fenofibrate could enhance the musculoskeletal training response during estrogen deficiency. We investigated the combined effects of 8 weeks of fenofibrate and jumping exercise in ovariectomized (OVX) Sprague Dawley rats. Female rats were allocated to a sham-operated group and four OVX groups; fenofibrate (OVX-Fen), exercise (OVX-Ex), combined fenofibrate and exercise (OVX-FenEx), and a control group (OVX-Ctr) (n = 12/group). Fenofibrate (90 mg/kg/d) or methylcellulose was given by gavage. The combination of exercise and fenofibrate resulted in enhanced femoral bone mineral density (BMD) and improved bone microarchitecture compared with fenofibrate alone as well as increased trabecular BMD compared with OVX-Ctr. These effects were not seen in the OVX-Ex group. Femoral BMD was normalized in both exercise groups relative to sham and increased more in all intervention groups compared with OVX-Ctr. A higher plasma level of the bone formation marker type 1 collagen amino propeptide was observed in the OVX-Fen and OVX-FenEx groups compared with controls. Lean mass and soleus muscle weight were higher in the OVX-FenEx group than in the OVX-Ctr group, which coincided with lower mRNA levels of Atrogin1. These results suggest that peroxisome proliferator-activated receptor-α activation improves the musculoskeletal effects of exercise during estrogen deficiency.</abstract><cop>United States</cop><pub>Endocrine Society</pub><pmid>27526032</pmid><doi>10.1210/en.2016-1114</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Agonists Animals Body Composition - drug effects Bone and Bones - drug effects Bone and Bones - metabolism Bone Density - drug effects Bone growth Bone mass Bone mineral density Cancellous bone Drug Evaluation, Preclinical Estrogens Estrogens - deficiency Female Femur Fenofibrate Fenofibrate - pharmacology Fenofibrate - therapeutic use Humans Jumping Methylcellulose mRNA Muscle, Skeletal - drug effects Muscle, Skeletal - metabolism Muscles Osteogenesis Osteogenesis - drug effects Ovariectomy Peroxisome proliferator-activated receptors Physical Conditioning, Animal PPAR alpha - agonists Random Allocation Rats, Sprague-Dawley Receptors Soleus muscle Tibia - diagnostic imaging Tibia - drug effects X-Ray Microtomography |
title | The PPARα Agonist Fenofibrate Improves the Musculoskeletal Effects of Exercise in Ovariectomized Rats |
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