Short‐term aerobic exercise prevents development of glucocorticoid myopathic features in aged skeletal muscle in a sex‐dependent manner
Older adults are vulnerable to glucocorticoid‐induced muscle atrophy and weakness, with sex potentially influencing their susceptibility to those effects. Aerobic exercise can reduce glucocorticoid‐induced muscle atrophy in young rodents. However, it is unknown whether aerobic exercise can prevent g...
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description | Older adults are vulnerable to glucocorticoid‐induced muscle atrophy and weakness, with sex potentially influencing their susceptibility to those effects. Aerobic exercise can reduce glucocorticoid‐induced muscle atrophy in young rodents. However, it is unknown whether aerobic exercise can prevent glucocorticoid myopathy in aged muscle. The objectives of this study were to define the extent to which sex influences the development of glucocorticoid myopathy in aged muscle, and to determine the extent to which aerobic exercise training protects against myopathy development. Twenty‐four‐month‐old female (n = 30) and male (n = 33) mice were randomized to either sedentary or aerobic exercise groups. Within their respective groups, mice were randomized to either daily treatment with dexamethasone (DEX) or saline. Upon completing treatments, the contractile properties of the triceps surae complex were assessed in situ. DEX marginally lowered muscle mass and soluble protein content in both sexes, which was attenuated by aerobic exercise only in females. DEX increased sub‐tetanic force and rate of force development only in females, which was not influenced by aerobic exercise. Muscle fatigue was higher in both sexes following DEX, but aerobic exercise prevented fatigue induction only in females. The sex‐specific differences to muscle function in response to DEX treatment coincided with sex‐specific changes to the content of proteins related to calcium handling, mitochondrial quality control, reactive oxygen species production, and glucocorticoid receptor in muscle. These findings define several important sexually dimorphic changes to aged skeletal muscle physiology in response to glucocorticoid treatment and define the capacity of short‐term aerobic exercise to protect against those changes.
Key points
There are sexually dimorphic effects of glucocorticoids on aged skeletal muscle physiology.
Glucocorticoid‐induced changes to aged muscle contractile properties coincide with sex‐specific differences in the content of calcium handling proteins.
Aerobic exercise prevents glucocorticoid‐induced fatigue only in aged females and coincides with differences in the content of mitochondrial quality control proteins and glucocorticoid receptors.
figure legend Daily 1 mg/kg dexamethasone (DEX) treatment in 24‐month‐old female and male mice results in sexually dimorphic effects on skeletal muscle physiology. Short‐term treadmill exercise mitigates the DEX‐induced myopathic feat |
doi_str_mv | 10.1113/JP286334 |
format | Article |
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Key points
There are sexually dimorphic effects of glucocorticoids on aged skeletal muscle physiology.
Glucocorticoid‐induced changes to aged muscle contractile properties coincide with sex‐specific differences in the content of calcium handling proteins.
Aerobic exercise prevents glucocorticoid‐induced fatigue only in aged females and coincides with differences in the content of mitochondrial quality control proteins and glucocorticoid receptors.
figure legend Daily 1 mg/kg dexamethasone (DEX) treatment in 24‐month‐old female and male mice results in sexually dimorphic effects on skeletal muscle physiology. Short‐term treadmill exercise mitigates the DEX‐induced myopathic features in a sex‐dependent manner. DEX‐treated aged female mice expressed greater sub‐tetanic contractility without an influence of exercise. Exercise protected against DEX‐induced fatigue and losses in muscle mass and soluble protein content in aged females. DEX treatment in aged male mice resulted in a prolonged tetanic half‐relaxation time, increased fatigue and losses in soluble protein content, which were not affected by exercise.</description><identifier>ISSN: 0022-3751</identifier><identifier>ISSN: 1469-7793</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1113/JP286334</identifier><identifier>PMID: 38861348</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Aerobic capacity ; Aerobics ; Atrophy ; Calcium (mitochondrial) ; calcium handling ; contractile function ; Dexamethasone ; Exercise ; Fatigue ; Females ; Glucocorticoid receptors ; Glucocorticoids ; Muscle contraction ; Musculoskeletal system ; Myopathy ; Physical fitness ; Physical training ; Physiology ; Proteins ; Quality control ; Reactive oxygen species ; Receptor mechanisms ; Sex ; Sexes ; Sexual dimorphism ; Skeletal muscle</subject><ispartof>The Journal of physiology, 2025-01, Vol.603 (1), p.127-149</ispartof><rights>2024 The Authors. © 2024 The Physiological Society.</rights><rights>2024 The Authors. The Journal of Physiology © 2024 The Physiological Society.</rights><rights>Journal compilation © 2025 The Physiological Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3117-b8c6f4e8728240f15612f391d7b239742a2764b2c126a0c700197c59a9cd0b853</cites><orcidid>0000-0001-9701-561X ; 0000-0002-3721-1085 ; 0000-0002-2806-8547 ; 0000-0001-9759-4017 ; 0000-0001-5322-0611</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1113%2FJP286334$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1113%2FJP286334$$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/38861348$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Laskin, Grant R.</creatorcontrib><creatorcontrib>Rentería, Liliana I.</creatorcontrib><creatorcontrib>Muller‐Delp, Judy M.</creatorcontrib><creatorcontrib>Kim, Jeong‐Su</creatorcontrib><creatorcontrib>Chase, P. Bryant</creatorcontrib><creatorcontrib>Hwang, Hyun Seok</creatorcontrib><creatorcontrib>Gordon, Bradley S.</creatorcontrib><title>Short‐term aerobic exercise prevents development of glucocorticoid myopathic features in aged skeletal muscle in a sex‐dependent manner</title><title>The Journal of physiology</title><addtitle>J Physiol</addtitle><description>Older adults are vulnerable to glucocorticoid‐induced muscle atrophy and weakness, with sex potentially influencing their susceptibility to those effects. Aerobic exercise can reduce glucocorticoid‐induced muscle atrophy in young rodents. However, it is unknown whether aerobic exercise can prevent glucocorticoid myopathy in aged muscle. The objectives of this study were to define the extent to which sex influences the development of glucocorticoid myopathy in aged muscle, and to determine the extent to which aerobic exercise training protects against myopathy development. Twenty‐four‐month‐old female (n = 30) and male (n = 33) mice were randomized to either sedentary or aerobic exercise groups. Within their respective groups, mice were randomized to either daily treatment with dexamethasone (DEX) or saline. Upon completing treatments, the contractile properties of the triceps surae complex were assessed in situ. DEX marginally lowered muscle mass and soluble protein content in both sexes, which was attenuated by aerobic exercise only in females. DEX increased sub‐tetanic force and rate of force development only in females, which was not influenced by aerobic exercise. Muscle fatigue was higher in both sexes following DEX, but aerobic exercise prevented fatigue induction only in females. The sex‐specific differences to muscle function in response to DEX treatment coincided with sex‐specific changes to the content of proteins related to calcium handling, mitochondrial quality control, reactive oxygen species production, and glucocorticoid receptor in muscle. These findings define several important sexually dimorphic changes to aged skeletal muscle physiology in response to glucocorticoid treatment and define the capacity of short‐term aerobic exercise to protect against those changes.
Key points
There are sexually dimorphic effects of glucocorticoids on aged skeletal muscle physiology.
Glucocorticoid‐induced changes to aged muscle contractile properties coincide with sex‐specific differences in the content of calcium handling proteins.
Aerobic exercise prevents glucocorticoid‐induced fatigue only in aged females and coincides with differences in the content of mitochondrial quality control proteins and glucocorticoid receptors.
figure legend Daily 1 mg/kg dexamethasone (DEX) treatment in 24‐month‐old female and male mice results in sexually dimorphic effects on skeletal muscle physiology. Short‐term treadmill exercise mitigates the DEX‐induced myopathic features in a sex‐dependent manner. DEX‐treated aged female mice expressed greater sub‐tetanic contractility without an influence of exercise. Exercise protected against DEX‐induced fatigue and losses in muscle mass and soluble protein content in aged females. DEX treatment in aged male mice resulted in a prolonged tetanic half‐relaxation time, increased fatigue and losses in soluble protein content, which were not affected by exercise.</description><subject>Aerobic capacity</subject><subject>Aerobics</subject><subject>Atrophy</subject><subject>Calcium (mitochondrial)</subject><subject>calcium handling</subject><subject>contractile function</subject><subject>Dexamethasone</subject><subject>Exercise</subject><subject>Fatigue</subject><subject>Females</subject><subject>Glucocorticoid receptors</subject><subject>Glucocorticoids</subject><subject>Muscle contraction</subject><subject>Musculoskeletal system</subject><subject>Myopathy</subject><subject>Physical fitness</subject><subject>Physical training</subject><subject>Physiology</subject><subject>Proteins</subject><subject>Quality control</subject><subject>Reactive oxygen species</subject><subject>Receptor mechanisms</subject><subject>Sex</subject><subject>Sexes</subject><subject>Sexual dimorphism</subject><subject>Skeletal muscle</subject><issn>0022-3751</issn><issn>1469-7793</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><recordid>eNp1kc1O3TAQRq2KqtzSSn0CZIkNm4DHTux4WSF-hQQSsI4cZwKhThzspOXu2LPpM_Ik9e0FFpW6Go115tiej5BvwPYAQOyfXfJSCpF_IAvIpc6U0mKDLBjjPBOqgE3yOcZ7xkAwrT-RTVGWEkReLsjz1Z0P08vT7wlDTw0GX3eW4iMG20WkY8CfOEyRNqk6P_apob6lt2623qbJzvquof3Sj2a6S5MtmmkOGGk3UHOLDY0_0OFkHO3naB3-PacRH9OVDY44NCtjb4YBwxfysTUu4tfXukVujg6vD06y84vj04Pv55kVACqrSyvbHEvFS56zFgoJvBUaGlVzoVXODVcyr7kFLg2zKn1bK1too23D6rIQW2R37R2Df5gxTlXfRYvOmQH9HCsBBSS7LFbozj_ovZ_DkF63piTItOp3oQ0-xoBtNYauN2FZAatWAVVvASV0-1U41z027-BbIgnYWwO_OofL_4qq67NLkFAo8QfaBpt1</recordid><startdate>20250101</startdate><enddate>20250101</enddate><creator>Laskin, Grant R.</creator><creator>Rentería, Liliana I.</creator><creator>Muller‐Delp, Judy M.</creator><creator>Kim, Jeong‐Su</creator><creator>Chase, P. Bryant</creator><creator>Hwang, Hyun Seok</creator><creator>Gordon, Bradley S.</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TS</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9701-561X</orcidid><orcidid>https://orcid.org/0000-0002-3721-1085</orcidid><orcidid>https://orcid.org/0000-0002-2806-8547</orcidid><orcidid>https://orcid.org/0000-0001-9759-4017</orcidid><orcidid>https://orcid.org/0000-0001-5322-0611</orcidid></search><sort><creationdate>20250101</creationdate><title>Short‐term aerobic exercise prevents development of glucocorticoid myopathic features in aged skeletal muscle in a sex‐dependent manner</title><author>Laskin, Grant R. ; Rentería, Liliana I. ; Muller‐Delp, Judy M. ; Kim, Jeong‐Su ; Chase, P. Bryant ; Hwang, Hyun Seok ; Gordon, Bradley S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3117-b8c6f4e8728240f15612f391d7b239742a2764b2c126a0c700197c59a9cd0b853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Aerobic capacity</topic><topic>Aerobics</topic><topic>Atrophy</topic><topic>Calcium (mitochondrial)</topic><topic>calcium handling</topic><topic>contractile function</topic><topic>Dexamethasone</topic><topic>Exercise</topic><topic>Fatigue</topic><topic>Females</topic><topic>Glucocorticoid receptors</topic><topic>Glucocorticoids</topic><topic>Muscle contraction</topic><topic>Musculoskeletal system</topic><topic>Myopathy</topic><topic>Physical fitness</topic><topic>Physical training</topic><topic>Physiology</topic><topic>Proteins</topic><topic>Quality control</topic><topic>Reactive oxygen species</topic><topic>Receptor mechanisms</topic><topic>Sex</topic><topic>Sexes</topic><topic>Sexual dimorphism</topic><topic>Skeletal muscle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Laskin, Grant R.</creatorcontrib><creatorcontrib>Rentería, Liliana I.</creatorcontrib><creatorcontrib>Muller‐Delp, Judy M.</creatorcontrib><creatorcontrib>Kim, Jeong‐Su</creatorcontrib><creatorcontrib>Chase, P. Bryant</creatorcontrib><creatorcontrib>Hwang, Hyun Seok</creatorcontrib><creatorcontrib>Gordon, Bradley S.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Laskin, Grant R.</au><au>Rentería, Liliana I.</au><au>Muller‐Delp, Judy M.</au><au>Kim, Jeong‐Su</au><au>Chase, P. Bryant</au><au>Hwang, Hyun Seok</au><au>Gordon, Bradley S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Short‐term aerobic exercise prevents development of glucocorticoid myopathic features in aged skeletal muscle in a sex‐dependent manner</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>2025-01-01</date><risdate>2025</risdate><volume>603</volume><issue>1</issue><spage>127</spage><epage>149</epage><pages>127-149</pages><issn>0022-3751</issn><issn>1469-7793</issn><eissn>1469-7793</eissn><abstract>Older adults are vulnerable to glucocorticoid‐induced muscle atrophy and weakness, with sex potentially influencing their susceptibility to those effects. Aerobic exercise can reduce glucocorticoid‐induced muscle atrophy in young rodents. However, it is unknown whether aerobic exercise can prevent glucocorticoid myopathy in aged muscle. The objectives of this study were to define the extent to which sex influences the development of glucocorticoid myopathy in aged muscle, and to determine the extent to which aerobic exercise training protects against myopathy development. Twenty‐four‐month‐old female (n = 30) and male (n = 33) mice were randomized to either sedentary or aerobic exercise groups. Within their respective groups, mice were randomized to either daily treatment with dexamethasone (DEX) or saline. Upon completing treatments, the contractile properties of the triceps surae complex were assessed in situ. DEX marginally lowered muscle mass and soluble protein content in both sexes, which was attenuated by aerobic exercise only in females. DEX increased sub‐tetanic force and rate of force development only in females, which was not influenced by aerobic exercise. Muscle fatigue was higher in both sexes following DEX, but aerobic exercise prevented fatigue induction only in females. The sex‐specific differences to muscle function in response to DEX treatment coincided with sex‐specific changes to the content of proteins related to calcium handling, mitochondrial quality control, reactive oxygen species production, and glucocorticoid receptor in muscle. These findings define several important sexually dimorphic changes to aged skeletal muscle physiology in response to glucocorticoid treatment and define the capacity of short‐term aerobic exercise to protect against those changes.
Key points
There are sexually dimorphic effects of glucocorticoids on aged skeletal muscle physiology.
Glucocorticoid‐induced changes to aged muscle contractile properties coincide with sex‐specific differences in the content of calcium handling proteins.
Aerobic exercise prevents glucocorticoid‐induced fatigue only in aged females and coincides with differences in the content of mitochondrial quality control proteins and glucocorticoid receptors.
figure legend Daily 1 mg/kg dexamethasone (DEX) treatment in 24‐month‐old female and male mice results in sexually dimorphic effects on skeletal muscle physiology. Short‐term treadmill exercise mitigates the DEX‐induced myopathic features in a sex‐dependent manner. DEX‐treated aged female mice expressed greater sub‐tetanic contractility without an influence of exercise. Exercise protected against DEX‐induced fatigue and losses in muscle mass and soluble protein content in aged females. DEX treatment in aged male mice resulted in a prolonged tetanic half‐relaxation time, increased fatigue and losses in soluble protein content, which were not affected by exercise.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38861348</pmid><doi>10.1113/JP286334</doi><tpages>23</tpages><orcidid>https://orcid.org/0000-0001-9701-561X</orcidid><orcidid>https://orcid.org/0000-0002-3721-1085</orcidid><orcidid>https://orcid.org/0000-0002-2806-8547</orcidid><orcidid>https://orcid.org/0000-0001-9759-4017</orcidid><orcidid>https://orcid.org/0000-0001-5322-0611</orcidid></addata></record> |
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subjects | Aerobic capacity Aerobics Atrophy Calcium (mitochondrial) calcium handling contractile function Dexamethasone Exercise Fatigue Females Glucocorticoid receptors Glucocorticoids Muscle contraction Musculoskeletal system Myopathy Physical fitness Physical training Physiology Proteins Quality control Reactive oxygen species Receptor mechanisms Sex Sexes Sexual dimorphism Skeletal muscle |
title | Short‐term aerobic exercise prevents development of glucocorticoid myopathic features in aged skeletal muscle in a sex‐dependent manner |
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