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Corticosteroid effects on isotonic contractile properties of rat diaphragm muscle
Roland H. H. Van Balkom 1 , Wen-Zhi Zhan 2 , Y. S. Prakash 2 , P. N. Richard Dekhuijzen 1 , and Gary C. Sieck 2 , 3 1 Department of Pulmonary Diseases, University Hospital Nijmegen, Nijmegen 6500 HB, The Netherlands; and Departments of 2 Anesthesiology, and 3 Physiology and Biophysics, Mayo Clini...
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Published in: | Journal of applied physiology (1985) 1997-10, Vol.83 (4), p.1062-1067 |
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creator | Van Balkom, Roland H. H Zhan, Wen-Zhi Prakash, Y. S Dekhuijzen, P. N. Richard Sieck, Gary C |
description | Roland H. H.
Van Balkom 1 ,
Wen-Zhi
Zhan 2 ,
Y. S.
Prakash 2 ,
P. N. Richard
Dekhuijzen 1 , and
Gary C.
Sieck 2 , 3
1 Department of Pulmonary Diseases, University
Hospital Nijmegen, Nijmegen 6500 HB, The Netherlands; and
Departments of 2 Anesthesiology,
and 3 Physiology and
Biophysics, Mayo Clinic and Foundation, Rochester, Minnesota 55905
Received 16 December 1996; accepted in final form 8 May 1997.
Van Balkom, Roland H. H., Wen-Zhi Zhan, Y. S. Prakash, P. N. Richard Dekhuijzen, and Gary C. Sieck. Corticosteroid effects on isotonic contractile properties of rat diaphragm muscle. J. Appl. Physiol. 83(4):
1062-1067, 1997. The effects of corticosteroids (CS) on diaphragm
muscle (Dia m ) fiber morphology
and contractile properties were evaluated in three groups of rats:
controls (Ctl), surgical sham and weight-matched controls (Sham), and
CS-treated (6 mg · kg 1 · day 1
prednisolone at 2.5 ml/h for 3 wk). In the CS-treated
Dia m , there was a selective
atrophy of type IIx and IIb fibers, compared with a generalized atrophy
of all fibers in the Sham group. Maximum isometric force was reduced by
20% in the CS group compared with both Ctl and Sham. Maximum
shortening velocity in the CS Dia m was slowed by ~20% compared with Ctl and Sham. Peak power output of
the CS Dia m was only 60% of Ctl
and 70% of Sham. Endurance to repeated isotonic contractions improved
in the CS-treated Dia m compared
with Ctl. We conclude that the atrophy of type IIx and IIb fibers in
the Dia m can only partially
account for the CS-induced changes in isotonic contractile properties.
Other factors such as reduced myofibrillar density or altered
cross-bridge cycling kinetics are also likely to contribute to the
effects of CS treatment.
prednisolone; skeletal muscle; fiber type; shortening velocity; fatigue; endurance
0161-7567/97 $5.00
Copyright © 1997 the American Physiological Society |
doi_str_mv | 10.1152/jappl.1997.83.4.1062 |
format | article |
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Van Balkom 1 ,
Wen-Zhi
Zhan 2 ,
Y. S.
Prakash 2 ,
P. N. Richard
Dekhuijzen 1 , and
Gary C.
Sieck 2 , 3
1 Department of Pulmonary Diseases, University
Hospital Nijmegen, Nijmegen 6500 HB, The Netherlands; and
Departments of 2 Anesthesiology,
and 3 Physiology and
Biophysics, Mayo Clinic and Foundation, Rochester, Minnesota 55905
Received 16 December 1996; accepted in final form 8 May 1997.
Van Balkom, Roland H. H., Wen-Zhi Zhan, Y. S. Prakash, P. N. Richard Dekhuijzen, and Gary C. Sieck. Corticosteroid effects on isotonic contractile properties of rat diaphragm muscle. J. Appl. Physiol. 83(4):
1062-1067, 1997. The effects of corticosteroids (CS) on diaphragm
muscle (Dia m ) fiber morphology
and contractile properties were evaluated in three groups of rats:
controls (Ctl), surgical sham and weight-matched controls (Sham), and
CS-treated (6 mg · kg 1 · day 1
prednisolone at 2.5 ml/h for 3 wk). In the CS-treated
Dia m , there was a selective
atrophy of type IIx and IIb fibers, compared with a generalized atrophy
of all fibers in the Sham group. Maximum isometric force was reduced by
20% in the CS group compared with both Ctl and Sham. Maximum
shortening velocity in the CS Dia m was slowed by ~20% compared with Ctl and Sham. Peak power output of
the CS Dia m was only 60% of Ctl
and 70% of Sham. Endurance to repeated isotonic contractions improved
in the CS-treated Dia m compared
with Ctl. We conclude that the atrophy of type IIx and IIb fibers in
the Dia m can only partially
account for the CS-induced changes in isotonic contractile properties.
Other factors such as reduced myofibrillar density or altered
cross-bridge cycling kinetics are also likely to contribute to the
effects of CS treatment.
prednisolone; skeletal muscle; fiber type; shortening velocity; fatigue; endurance
0161-7567/97 $5.00
Copyright © 1997 the American Physiological Society</description><identifier>ISSN: 8750-7587</identifier><identifier>EISSN: 1522-1601</identifier><identifier>DOI: 10.1152/jappl.1997.83.4.1062</identifier><identifier>PMID: 9338411</identifier><identifier>CODEN: JAPHEV</identifier><language>eng</language><publisher>Bethesda, MD: Am Physiological Soc</publisher><subject>Adrenal Cortex Hormones - pharmacology ; Animals ; Biological and medical sciences ; Diaphragm - cytology ; Diaphragm - drug effects ; Glucocorticoids - pharmacology ; Hormones. Endocrine system ; Isotonic Contraction - drug effects ; Kinetics ; Male ; Medical sciences ; Muscle Contraction - drug effects ; Muscle Fibers, Skeletal - drug effects ; Muscle Fibers, Skeletal - physiology ; Muscle Fibers, Skeletal - ultrastructure ; Myosin Heavy Chains - metabolism ; Pharmacology. Drug treatments ; Physical Endurance - drug effects ; Physical Endurance - physiology ; Prednisolone - pharmacology ; Rats ; Rats, Sprague-Dawley ; Space life sciences</subject><ispartof>Journal of applied physiology (1985), 1997-10, Vol.83 (4), p.1062-1067</ispartof><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-59bb793ba889942cb85f5f603d747d72379b6065205476f55b513a938d1e0e783</citedby><cites>FETCH-LOGICAL-c455t-59bb793ba889942cb85f5f603d747d72379b6065205476f55b513a938d1e0e783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2841361$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9338411$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Van Balkom, Roland H. H</creatorcontrib><creatorcontrib>Zhan, Wen-Zhi</creatorcontrib><creatorcontrib>Prakash, Y. S</creatorcontrib><creatorcontrib>Dekhuijzen, P. N. Richard</creatorcontrib><creatorcontrib>Sieck, Gary C</creatorcontrib><title>Corticosteroid effects on isotonic contractile properties of rat diaphragm muscle</title><title>Journal of applied physiology (1985)</title><addtitle>J Appl Physiol (1985)</addtitle><description>Roland H. H.
Van Balkom 1 ,
Wen-Zhi
Zhan 2 ,
Y. S.
Prakash 2 ,
P. N. Richard
Dekhuijzen 1 , and
Gary C.
Sieck 2 , 3
1 Department of Pulmonary Diseases, University
Hospital Nijmegen, Nijmegen 6500 HB, The Netherlands; and
Departments of 2 Anesthesiology,
and 3 Physiology and
Biophysics, Mayo Clinic and Foundation, Rochester, Minnesota 55905
Received 16 December 1996; accepted in final form 8 May 1997.
Van Balkom, Roland H. H., Wen-Zhi Zhan, Y. S. Prakash, P. N. Richard Dekhuijzen, and Gary C. Sieck. Corticosteroid effects on isotonic contractile properties of rat diaphragm muscle. J. Appl. Physiol. 83(4):
1062-1067, 1997. The effects of corticosteroids (CS) on diaphragm
muscle (Dia m ) fiber morphology
and contractile properties were evaluated in three groups of rats:
controls (Ctl), surgical sham and weight-matched controls (Sham), and
CS-treated (6 mg · kg 1 · day 1
prednisolone at 2.5 ml/h for 3 wk). In the CS-treated
Dia m , there was a selective
atrophy of type IIx and IIb fibers, compared with a generalized atrophy
of all fibers in the Sham group. Maximum isometric force was reduced by
20% in the CS group compared with both Ctl and Sham. Maximum
shortening velocity in the CS Dia m was slowed by ~20% compared with Ctl and Sham. Peak power output of
the CS Dia m was only 60% of Ctl
and 70% of Sham. Endurance to repeated isotonic contractions improved
in the CS-treated Dia m compared
with Ctl. We conclude that the atrophy of type IIx and IIb fibers in
the Dia m can only partially
account for the CS-induced changes in isotonic contractile properties.
Other factors such as reduced myofibrillar density or altered
cross-bridge cycling kinetics are also likely to contribute to the
effects of CS treatment.
prednisolone; skeletal muscle; fiber type; shortening velocity; fatigue; endurance
0161-7567/97 $5.00
Copyright © 1997 the American Physiological Society</description><subject>Adrenal Cortex Hormones - pharmacology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Diaphragm - cytology</subject><subject>Diaphragm - drug effects</subject><subject>Glucocorticoids - pharmacology</subject><subject>Hormones. Endocrine system</subject><subject>Isotonic Contraction - drug effects</subject><subject>Kinetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle Fibers, Skeletal - drug effects</subject><subject>Muscle Fibers, Skeletal - physiology</subject><subject>Muscle Fibers, Skeletal - ultrastructure</subject><subject>Myosin Heavy Chains - metabolism</subject><subject>Pharmacology. Drug treatments</subject><subject>Physical Endurance - drug effects</subject><subject>Physical Endurance - physiology</subject><subject>Prednisolone - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Space life sciences</subject><issn>8750-7587</issn><issn>1522-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNp1kEFrHCEYhqW0JJu0_6CFOZSSy0x11FGPYWmSQqAU0rM4ju4anHGiDu3--zrdZSGHnjy8z_N-8gLwEcEGIdp-fVbz7BskBGs4bkiDYNe-AZsStTXqIHoLNpxRWDPK2SW4SukZQkQIRRfgQmDMCUIb8HMbYnY6pGxicENlrDU6pypMlUshh8npSocpR6Wz86aaY5hNMUxBbBVVrgan5n1Uu7Eal6S9eQ_eWeWT-XB6r8Gvu29P24f68cf99-3tY60Jpbmmou-ZwL3iXAjS6p5TS20H8cAIG1iLmeg72NEWUsI6S2lPEVYC8wEZaBjH1-DLsbd86WUxKcvRJW28V5MJS5KlnELIRQHJEdQxpBSNlXN0o4oHiaBcl5T_lpTrkpJjSeS6ZNE-nfqXfjTDWTpNV_LPp1wlrbyNatIunbG2QLhbsZsjtne7_W8XjZz3h-SCD7vDevjVRfJ_9G7x_sn8yatzVuQ8WPwXkp-eYg</recordid><startdate>19971001</startdate><enddate>19971001</enddate><creator>Van Balkom, Roland H. H</creator><creator>Zhan, Wen-Zhi</creator><creator>Prakash, Y. S</creator><creator>Dekhuijzen, P. N. Richard</creator><creator>Sieck, Gary C</creator><general>Am Physiological Soc</general><general>American Physiological Society</general><scope>IQODW</scope><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>19971001</creationdate><title>Corticosteroid effects on isotonic contractile properties of rat diaphragm muscle</title><author>Van Balkom, Roland H. H ; Zhan, Wen-Zhi ; Prakash, Y. S ; Dekhuijzen, P. N. Richard ; Sieck, Gary C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-59bb793ba889942cb85f5f603d747d72379b6065205476f55b513a938d1e0e783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adrenal Cortex Hormones - pharmacology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Diaphragm - cytology</topic><topic>Diaphragm - drug effects</topic><topic>Glucocorticoids - pharmacology</topic><topic>Hormones. Endocrine system</topic><topic>Isotonic Contraction - drug effects</topic><topic>Kinetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle Fibers, Skeletal - drug effects</topic><topic>Muscle Fibers, Skeletal - physiology</topic><topic>Muscle Fibers, Skeletal - ultrastructure</topic><topic>Myosin Heavy Chains - metabolism</topic><topic>Pharmacology. Drug treatments</topic><topic>Physical Endurance - drug effects</topic><topic>Physical Endurance - physiology</topic><topic>Prednisolone - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Space life sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Van Balkom, Roland H. H</creatorcontrib><creatorcontrib>Zhan, Wen-Zhi</creatorcontrib><creatorcontrib>Prakash, Y. S</creatorcontrib><creatorcontrib>Dekhuijzen, P. N. Richard</creatorcontrib><creatorcontrib>Sieck, Gary C</creatorcontrib><collection>Pascal-Francis</collection><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>Journal of applied physiology (1985)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Van Balkom, Roland H. H</au><au>Zhan, Wen-Zhi</au><au>Prakash, Y. S</au><au>Dekhuijzen, P. N. Richard</au><au>Sieck, Gary C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Corticosteroid effects on isotonic contractile properties of rat diaphragm muscle</atitle><jtitle>Journal of applied physiology (1985)</jtitle><addtitle>J Appl Physiol (1985)</addtitle><date>1997-10-01</date><risdate>1997</risdate><volume>83</volume><issue>4</issue><spage>1062</spage><epage>1067</epage><pages>1062-1067</pages><issn>8750-7587</issn><eissn>1522-1601</eissn><coden>JAPHEV</coden><abstract>Roland H. H.
Van Balkom 1 ,
Wen-Zhi
Zhan 2 ,
Y. S.
Prakash 2 ,
P. N. Richard
Dekhuijzen 1 , and
Gary C.
Sieck 2 , 3
1 Department of Pulmonary Diseases, University
Hospital Nijmegen, Nijmegen 6500 HB, The Netherlands; and
Departments of 2 Anesthesiology,
and 3 Physiology and
Biophysics, Mayo Clinic and Foundation, Rochester, Minnesota 55905
Received 16 December 1996; accepted in final form 8 May 1997.
Van Balkom, Roland H. H., Wen-Zhi Zhan, Y. S. Prakash, P. N. Richard Dekhuijzen, and Gary C. Sieck. Corticosteroid effects on isotonic contractile properties of rat diaphragm muscle. J. Appl. Physiol. 83(4):
1062-1067, 1997. The effects of corticosteroids (CS) on diaphragm
muscle (Dia m ) fiber morphology
and contractile properties were evaluated in three groups of rats:
controls (Ctl), surgical sham and weight-matched controls (Sham), and
CS-treated (6 mg · kg 1 · day 1
prednisolone at 2.5 ml/h for 3 wk). In the CS-treated
Dia m , there was a selective
atrophy of type IIx and IIb fibers, compared with a generalized atrophy
of all fibers in the Sham group. Maximum isometric force was reduced by
20% in the CS group compared with both Ctl and Sham. Maximum
shortening velocity in the CS Dia m was slowed by ~20% compared with Ctl and Sham. Peak power output of
the CS Dia m was only 60% of Ctl
and 70% of Sham. Endurance to repeated isotonic contractions improved
in the CS-treated Dia m compared
with Ctl. We conclude that the atrophy of type IIx and IIb fibers in
the Dia m can only partially
account for the CS-induced changes in isotonic contractile properties.
Other factors such as reduced myofibrillar density or altered
cross-bridge cycling kinetics are also likely to contribute to the
effects of CS treatment.
prednisolone; skeletal muscle; fiber type; shortening velocity; fatigue; endurance
0161-7567/97 $5.00
Copyright © 1997 the American Physiological Society</abstract><cop>Bethesda, MD</cop><pub>Am Physiological Soc</pub><pmid>9338411</pmid><doi>10.1152/jappl.1997.83.4.1062</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | American Physiological Society Free |
subjects | Adrenal Cortex Hormones - pharmacology Animals Biological and medical sciences Diaphragm - cytology Diaphragm - drug effects Glucocorticoids - pharmacology Hormones. Endocrine system Isotonic Contraction - drug effects Kinetics Male Medical sciences Muscle Contraction - drug effects Muscle Fibers, Skeletal - drug effects Muscle Fibers, Skeletal - physiology Muscle Fibers, Skeletal - ultrastructure Myosin Heavy Chains - metabolism Pharmacology. Drug treatments Physical Endurance - drug effects Physical Endurance - physiology Prednisolone - pharmacology Rats Rats, Sprague-Dawley Space life sciences |
title | Corticosteroid effects on isotonic contractile properties of rat diaphragm muscle |
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