Muscle hypertrophy following blood flow-restricted, low-force isometric electrical stimulation in rat tibialis anterior: role for muscle hypoxia

Low-force exercise training with blood flow restriction (BFR) elicits muscle hypertrophy as seen typically after higher-force exercise. We investigated the effects of microvascular hypoxia [i.e., low microvascular O partial pressures (P mvO )] during contractions on muscle hypertrophic signaling, gr...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of applied physiology (1985) 2018-07, Vol.125 (1), p.134-145
Hauptverfasser: Nakajima, Toshiaki, Koide, Seiichiro, Yasuda, Tomohiro, Hasegawa, Takaaki, Yamasoba, Tatsuya, Obi, Syotaro, Toyoda, Shigeru, Nakamura, Fumitaka, Inoue, Teruo, Poole, David C, Kano, Yutaka
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 145
container_issue 1
container_start_page 134
container_title Journal of applied physiology (1985)
container_volume 125
creator Nakajima, Toshiaki
Koide, Seiichiro
Yasuda, Tomohiro
Hasegawa, Takaaki
Yamasoba, Tatsuya
Obi, Syotaro
Toyoda, Shigeru
Nakamura, Fumitaka
Inoue, Teruo
Poole, David C
Kano, Yutaka
description Low-force exercise training with blood flow restriction (BFR) elicits muscle hypertrophy as seen typically after higher-force exercise. We investigated the effects of microvascular hypoxia [i.e., low microvascular O partial pressures (P mvO )] during contractions on muscle hypertrophic signaling, growth response, and key muscle adaptations for increasing exercise capacity. Wistar rats were fitted with a cuff placed around the upper thigh and inflated to restrict limb blood flow. Low-force isometric contractions (30 Hz) were evoked via electrical stimulation of the tibialis anterior (TA) muscle. The P mvO was determined by phosphorescence quenching. Rats underwent acute and chronic stimulation protocols. Whereas P mvO decreased transiently with 30 Hz contractions, simultaneous BFR induced severe hypoxia, reducing P mvO lower than present for maximal (100 Hz) contractions. Low-force electrical stimulation (EXER) induced muscle hypertrophy (6.2%, P < 0.01), whereas control group conditions or BFR alone did not. EXER+BFR also induced an increase in muscle mass (11.0%, P < 0.01) and, unique among conditions studied, significantly increased fiber cross-sectional area in the superficial TA ( P < 0.05). Phosphorylation of ribosomal protein S6 was enhanced by EXER+BFR, as were peroxisome proliferator-activated receptor gamma coactivator-1α and glucose transporter 4 protein levels. Fibronectin type III domain-containing protein 5, cytochrome c oxidase subunit 4, monocarboxylate transporter 1 (MCT1), and cluster of differentiation 147 increased with EXER alone. EXER+BFR significantly increased MCT1 expression more than EXER alone. These data demonstrate that microvascular hypoxia during contractions is not essential for hypertrophy. However, hypoxia induced via BFR may potentiate the muscle hypertrophic response (as evidenced by the increased superficial fiber cross-sectional area) with increased glucose transporter and mitochondrial biogenesis, which contributes to the pleiotropic effects of exercise training with BFR that culminate in an improved capacity for sustained exercise. NEW & NOTEWORTHY We investigated the effects of low microvascular O partial pressures (P mvO ) during contractions on muscle hypertrophic signaling and key elements in the muscle adaptation for increasing exercise capacity. Although demonstrating that muscle hypoxia is not obligatory for the hypertrophic response to low-force, electrically induced muscle contractions, the reduced P mvO enha
doi_str_mv 10.1152/japplphysiol.00972.2017
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2018017322</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2018017322</sourcerecordid><originalsourceid>FETCH-LOGICAL-c428t-15c44f8471d38c03ccd7baf4e36e62c4ce815a714ee7150f3cb46e78ceb8f6b3</originalsourceid><addsrcrecordid>eNpNUctOJSEUJMaJXh-_oCxd2HeAhgbdmRsfkziZjfsOTR8UQzct0NH7F_PJQ_vKrOAcTlUdqhA6pWRNqWA_n_U0-elpm1zwa0IuJFszQuUOWpVXVtGG0F20UlKQSgol99FBSs-EUM4F3UP77EI0Qkq-Qn9_z8l4wE_bCWKOoXBiG7wPr258xJ0Poce2VFWElKMzGfpzvNQ2RAPYpTDA0sfgwSwX7XHKbpi9zi6M2I046oyz65z2LmE9ZoguxEscQ5EtLHj43iC8OX2EfljtExx_nofo4eb6YXNX3f-5_bW5uq8MZypXVBjOreKS9rUypDaml522HOoGGma4AUWFlpQDSCqIrU3HG5DKQKds09WH6OyDdorhZS5_aweXDHivRwhzaoubqhhaM1ZG5ceoiSGlCLadoht03LaUtEsa7f9ptO9pLHhZkCefInM3QP-N-7K__gfRKo87</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2018017322</pqid></control><display><type>article</type><title>Muscle hypertrophy following blood flow-restricted, low-force isometric electrical stimulation in rat tibialis anterior: role for muscle hypoxia</title><source>American Physiological Society</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Nakajima, Toshiaki ; Koide, Seiichiro ; Yasuda, Tomohiro ; Hasegawa, Takaaki ; Yamasoba, Tatsuya ; Obi, Syotaro ; Toyoda, Shigeru ; Nakamura, Fumitaka ; Inoue, Teruo ; Poole, David C ; Kano, Yutaka</creator><creatorcontrib>Nakajima, Toshiaki ; Koide, Seiichiro ; Yasuda, Tomohiro ; Hasegawa, Takaaki ; Yamasoba, Tatsuya ; Obi, Syotaro ; Toyoda, Shigeru ; Nakamura, Fumitaka ; Inoue, Teruo ; Poole, David C ; Kano, Yutaka</creatorcontrib><description>Low-force exercise training with blood flow restriction (BFR) elicits muscle hypertrophy as seen typically after higher-force exercise. We investigated the effects of microvascular hypoxia [i.e., low microvascular O partial pressures (P mvO )] during contractions on muscle hypertrophic signaling, growth response, and key muscle adaptations for increasing exercise capacity. Wistar rats were fitted with a cuff placed around the upper thigh and inflated to restrict limb blood flow. Low-force isometric contractions (30 Hz) were evoked via electrical stimulation of the tibialis anterior (TA) muscle. The P mvO was determined by phosphorescence quenching. Rats underwent acute and chronic stimulation protocols. Whereas P mvO decreased transiently with 30 Hz contractions, simultaneous BFR induced severe hypoxia, reducing P mvO lower than present for maximal (100 Hz) contractions. Low-force electrical stimulation (EXER) induced muscle hypertrophy (6.2%, P &lt; 0.01), whereas control group conditions or BFR alone did not. EXER+BFR also induced an increase in muscle mass (11.0%, P &lt; 0.01) and, unique among conditions studied, significantly increased fiber cross-sectional area in the superficial TA ( P &lt; 0.05). Phosphorylation of ribosomal protein S6 was enhanced by EXER+BFR, as were peroxisome proliferator-activated receptor gamma coactivator-1α and glucose transporter 4 protein levels. Fibronectin type III domain-containing protein 5, cytochrome c oxidase subunit 4, monocarboxylate transporter 1 (MCT1), and cluster of differentiation 147 increased with EXER alone. EXER+BFR significantly increased MCT1 expression more than EXER alone. These data demonstrate that microvascular hypoxia during contractions is not essential for hypertrophy. However, hypoxia induced via BFR may potentiate the muscle hypertrophic response (as evidenced by the increased superficial fiber cross-sectional area) with increased glucose transporter and mitochondrial biogenesis, which contributes to the pleiotropic effects of exercise training with BFR that culminate in an improved capacity for sustained exercise. NEW &amp; NOTEWORTHY We investigated the effects of low microvascular O partial pressures (P mvO ) during contractions on muscle hypertrophic signaling and key elements in the muscle adaptation for increasing exercise capacity. Although demonstrating that muscle hypoxia is not obligatory for the hypertrophic response to low-force, electrically induced muscle contractions, the reduced P mvO enhanced ribosomal protein S6 phosphorylation and potentiated the hypertrophic response. Furthermore, contractions with blood flow restriction increased oxidative capacity, glucose transporter, and mitochondrial biogenesis, which are key determinants of the pleiotropic effects of exercise training.</description><identifier>ISSN: 8750-7587</identifier><identifier>EISSN: 1522-1601</identifier><identifier>DOI: 10.1152/japplphysiol.00972.2017</identifier><identifier>PMID: 29565774</identifier><language>eng</language><publisher>United States</publisher><ispartof>Journal of applied physiology (1985), 2018-07, Vol.125 (1), p.134-145</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-15c44f8471d38c03ccd7baf4e36e62c4ce815a714ee7150f3cb46e78ceb8f6b3</citedby><cites>FETCH-LOGICAL-c428t-15c44f8471d38c03ccd7baf4e36e62c4ce815a714ee7150f3cb46e78ceb8f6b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3025,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29565774$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakajima, Toshiaki</creatorcontrib><creatorcontrib>Koide, Seiichiro</creatorcontrib><creatorcontrib>Yasuda, Tomohiro</creatorcontrib><creatorcontrib>Hasegawa, Takaaki</creatorcontrib><creatorcontrib>Yamasoba, Tatsuya</creatorcontrib><creatorcontrib>Obi, Syotaro</creatorcontrib><creatorcontrib>Toyoda, Shigeru</creatorcontrib><creatorcontrib>Nakamura, Fumitaka</creatorcontrib><creatorcontrib>Inoue, Teruo</creatorcontrib><creatorcontrib>Poole, David C</creatorcontrib><creatorcontrib>Kano, Yutaka</creatorcontrib><title>Muscle hypertrophy following blood flow-restricted, low-force isometric electrical stimulation in rat tibialis anterior: role for muscle hypoxia</title><title>Journal of applied physiology (1985)</title><addtitle>J Appl Physiol (1985)</addtitle><description>Low-force exercise training with blood flow restriction (BFR) elicits muscle hypertrophy as seen typically after higher-force exercise. We investigated the effects of microvascular hypoxia [i.e., low microvascular O partial pressures (P mvO )] during contractions on muscle hypertrophic signaling, growth response, and key muscle adaptations for increasing exercise capacity. Wistar rats were fitted with a cuff placed around the upper thigh and inflated to restrict limb blood flow. Low-force isometric contractions (30 Hz) were evoked via electrical stimulation of the tibialis anterior (TA) muscle. The P mvO was determined by phosphorescence quenching. Rats underwent acute and chronic stimulation protocols. Whereas P mvO decreased transiently with 30 Hz contractions, simultaneous BFR induced severe hypoxia, reducing P mvO lower than present for maximal (100 Hz) contractions. Low-force electrical stimulation (EXER) induced muscle hypertrophy (6.2%, P &lt; 0.01), whereas control group conditions or BFR alone did not. EXER+BFR also induced an increase in muscle mass (11.0%, P &lt; 0.01) and, unique among conditions studied, significantly increased fiber cross-sectional area in the superficial TA ( P &lt; 0.05). Phosphorylation of ribosomal protein S6 was enhanced by EXER+BFR, as were peroxisome proliferator-activated receptor gamma coactivator-1α and glucose transporter 4 protein levels. Fibronectin type III domain-containing protein 5, cytochrome c oxidase subunit 4, monocarboxylate transporter 1 (MCT1), and cluster of differentiation 147 increased with EXER alone. EXER+BFR significantly increased MCT1 expression more than EXER alone. These data demonstrate that microvascular hypoxia during contractions is not essential for hypertrophy. However, hypoxia induced via BFR may potentiate the muscle hypertrophic response (as evidenced by the increased superficial fiber cross-sectional area) with increased glucose transporter and mitochondrial biogenesis, which contributes to the pleiotropic effects of exercise training with BFR that culminate in an improved capacity for sustained exercise. NEW &amp; NOTEWORTHY We investigated the effects of low microvascular O partial pressures (P mvO ) during contractions on muscle hypertrophic signaling and key elements in the muscle adaptation for increasing exercise capacity. Although demonstrating that muscle hypoxia is not obligatory for the hypertrophic response to low-force, electrically induced muscle contractions, the reduced P mvO enhanced ribosomal protein S6 phosphorylation and potentiated the hypertrophic response. Furthermore, contractions with blood flow restriction increased oxidative capacity, glucose transporter, and mitochondrial biogenesis, which are key determinants of the pleiotropic effects of exercise training.</description><issn>8750-7587</issn><issn>1522-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpNUctOJSEUJMaJXh-_oCxd2HeAhgbdmRsfkziZjfsOTR8UQzct0NH7F_PJQ_vKrOAcTlUdqhA6pWRNqWA_n_U0-elpm1zwa0IuJFszQuUOWpVXVtGG0F20UlKQSgol99FBSs-EUM4F3UP77EI0Qkq-Qn9_z8l4wE_bCWKOoXBiG7wPr258xJ0Poce2VFWElKMzGfpzvNQ2RAPYpTDA0sfgwSwX7XHKbpi9zi6M2I046oyz65z2LmE9ZoguxEscQ5EtLHj43iC8OX2EfljtExx_nofo4eb6YXNX3f-5_bW5uq8MZypXVBjOreKS9rUypDaml522HOoGGma4AUWFlpQDSCqIrU3HG5DKQKds09WH6OyDdorhZS5_aweXDHivRwhzaoubqhhaM1ZG5ceoiSGlCLadoht03LaUtEsa7f9ptO9pLHhZkCefInM3QP-N-7K__gfRKo87</recordid><startdate>20180701</startdate><enddate>20180701</enddate><creator>Nakajima, Toshiaki</creator><creator>Koide, Seiichiro</creator><creator>Yasuda, Tomohiro</creator><creator>Hasegawa, Takaaki</creator><creator>Yamasoba, Tatsuya</creator><creator>Obi, Syotaro</creator><creator>Toyoda, Shigeru</creator><creator>Nakamura, Fumitaka</creator><creator>Inoue, Teruo</creator><creator>Poole, David C</creator><creator>Kano, Yutaka</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20180701</creationdate><title>Muscle hypertrophy following blood flow-restricted, low-force isometric electrical stimulation in rat tibialis anterior: role for muscle hypoxia</title><author>Nakajima, Toshiaki ; Koide, Seiichiro ; Yasuda, Tomohiro ; Hasegawa, Takaaki ; Yamasoba, Tatsuya ; Obi, Syotaro ; Toyoda, Shigeru ; Nakamura, Fumitaka ; Inoue, Teruo ; Poole, David C ; Kano, Yutaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-15c44f8471d38c03ccd7baf4e36e62c4ce815a714ee7150f3cb46e78ceb8f6b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakajima, Toshiaki</creatorcontrib><creatorcontrib>Koide, Seiichiro</creatorcontrib><creatorcontrib>Yasuda, Tomohiro</creatorcontrib><creatorcontrib>Hasegawa, Takaaki</creatorcontrib><creatorcontrib>Yamasoba, Tatsuya</creatorcontrib><creatorcontrib>Obi, Syotaro</creatorcontrib><creatorcontrib>Toyoda, Shigeru</creatorcontrib><creatorcontrib>Nakamura, Fumitaka</creatorcontrib><creatorcontrib>Inoue, Teruo</creatorcontrib><creatorcontrib>Poole, David C</creatorcontrib><creatorcontrib>Kano, Yutaka</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of applied physiology (1985)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakajima, Toshiaki</au><au>Koide, Seiichiro</au><au>Yasuda, Tomohiro</au><au>Hasegawa, Takaaki</au><au>Yamasoba, Tatsuya</au><au>Obi, Syotaro</au><au>Toyoda, Shigeru</au><au>Nakamura, Fumitaka</au><au>Inoue, Teruo</au><au>Poole, David C</au><au>Kano, Yutaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Muscle hypertrophy following blood flow-restricted, low-force isometric electrical stimulation in rat tibialis anterior: role for muscle hypoxia</atitle><jtitle>Journal of applied physiology (1985)</jtitle><addtitle>J Appl Physiol (1985)</addtitle><date>2018-07-01</date><risdate>2018</risdate><volume>125</volume><issue>1</issue><spage>134</spage><epage>145</epage><pages>134-145</pages><issn>8750-7587</issn><eissn>1522-1601</eissn><abstract>Low-force exercise training with blood flow restriction (BFR) elicits muscle hypertrophy as seen typically after higher-force exercise. We investigated the effects of microvascular hypoxia [i.e., low microvascular O partial pressures (P mvO )] during contractions on muscle hypertrophic signaling, growth response, and key muscle adaptations for increasing exercise capacity. Wistar rats were fitted with a cuff placed around the upper thigh and inflated to restrict limb blood flow. Low-force isometric contractions (30 Hz) were evoked via electrical stimulation of the tibialis anterior (TA) muscle. The P mvO was determined by phosphorescence quenching. Rats underwent acute and chronic stimulation protocols. Whereas P mvO decreased transiently with 30 Hz contractions, simultaneous BFR induced severe hypoxia, reducing P mvO lower than present for maximal (100 Hz) contractions. Low-force electrical stimulation (EXER) induced muscle hypertrophy (6.2%, P &lt; 0.01), whereas control group conditions or BFR alone did not. EXER+BFR also induced an increase in muscle mass (11.0%, P &lt; 0.01) and, unique among conditions studied, significantly increased fiber cross-sectional area in the superficial TA ( P &lt; 0.05). Phosphorylation of ribosomal protein S6 was enhanced by EXER+BFR, as were peroxisome proliferator-activated receptor gamma coactivator-1α and glucose transporter 4 protein levels. Fibronectin type III domain-containing protein 5, cytochrome c oxidase subunit 4, monocarboxylate transporter 1 (MCT1), and cluster of differentiation 147 increased with EXER alone. EXER+BFR significantly increased MCT1 expression more than EXER alone. These data demonstrate that microvascular hypoxia during contractions is not essential for hypertrophy. However, hypoxia induced via BFR may potentiate the muscle hypertrophic response (as evidenced by the increased superficial fiber cross-sectional area) with increased glucose transporter and mitochondrial biogenesis, which contributes to the pleiotropic effects of exercise training with BFR that culminate in an improved capacity for sustained exercise. NEW &amp; NOTEWORTHY We investigated the effects of low microvascular O partial pressures (P mvO ) during contractions on muscle hypertrophic signaling and key elements in the muscle adaptation for increasing exercise capacity. Although demonstrating that muscle hypoxia is not obligatory for the hypertrophic response to low-force, electrically induced muscle contractions, the reduced P mvO enhanced ribosomal protein S6 phosphorylation and potentiated the hypertrophic response. Furthermore, contractions with blood flow restriction increased oxidative capacity, glucose transporter, and mitochondrial biogenesis, which are key determinants of the pleiotropic effects of exercise training.</abstract><cop>United States</cop><pmid>29565774</pmid><doi>10.1152/japplphysiol.00972.2017</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 8750-7587
ispartof Journal of applied physiology (1985), 2018-07, Vol.125 (1), p.134-145
issn 8750-7587
1522-1601
language eng
recordid cdi_proquest_miscellaneous_2018017322
source American Physiological Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
title Muscle hypertrophy following blood flow-restricted, low-force isometric electrical stimulation in rat tibialis anterior: role for muscle hypoxia
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T08%3A28%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Muscle%20hypertrophy%20following%20blood%20flow-restricted,%20low-force%20isometric%20electrical%20stimulation%20in%20rat%20tibialis%20anterior:%20role%20for%20muscle%20hypoxia&rft.jtitle=Journal%20of%20applied%20physiology%20(1985)&rft.au=Nakajima,%20Toshiaki&rft.date=2018-07-01&rft.volume=125&rft.issue=1&rft.spage=134&rft.epage=145&rft.pages=134-145&rft.issn=8750-7587&rft.eissn=1522-1601&rft_id=info:doi/10.1152/japplphysiol.00972.2017&rft_dat=%3Cproquest_cross%3E2018017322%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2018017322&rft_id=info:pmid/29565774&rfr_iscdi=true