Adjustable passive length-tension curve in rabbit detrusor smooth muscle
Departments of 1 Mechanical Engineering, 2 Biomedical Engineering, 3 Surgery, 4 Biochemistry, and 5 Pediatrics, Virginia Commonwealth University, Richmond, Virginia Submitted 15 May 2006 ; accepted in final form 11 January 2007 Until the 1990s, the passive and active length-tension ( L -T) relations...
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container_title | Journal of applied physiology (1985) |
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creator | Speich, John E Dosier, Christopher Borgsmiller, Lindsey Quintero, Kevin Koo, Harry P Ratz, Paul H |
description | Departments of 1 Mechanical Engineering, 2 Biomedical Engineering, 3 Surgery, 4 Biochemistry, and 5 Pediatrics, Virginia Commonwealth University, Richmond, Virginia
Submitted 15 May 2006
; accepted in final form 11 January 2007
Until the 1990s, the passive and active length-tension ( L -T) relationships of smooth muscle were believed to be static, with a single passive force value and a single maximum active force value for each muscle length. However, recent studies have demonstrated that the active L -T relationship in airway smooth muscle is dynamic and adapts to length changes over a period of time. Furthermore, our prior work showed that the passive L -T relationship in rabbit detrusor smooth muscle (DSM) is also dynamic and that in addition to viscoelastic behavior, DSM displays strain-softening behavior characterized by a loss of passive stiffness at shorter lengths following a stretch to a new longer length. This loss of passive stiffness appears to be irreversible when the muscle is not producing active force and during submaximal activation but is reversible on full muscle activation, which indicates that the stiffness component of passive force lost to strain softening is adjustable in DSM. The present study demonstrates that the passive L -T curve for DSM is not static and can shift along the length axis as a function of strain history and activation history. This study also demonstrates that adjustable passive stiffness (APS) can modulate total force (35% increase) for a given muscle length, while active force remains relatively unchanged (4% increase). This finding suggests that the structures responsible for APS act in parallel with the contractile apparatus, and the results are used to further justify the configuration of modeling elements within our previously proposed mechanical model for APS.
muscle mechanics; preconditioning; strain softening; passive force; active force
Address for reprint requests and other correspondence: J. E. Speich, Virginia Commonwealth Univ., Dept. of Mechanical Engineering, 601 West Main St., P.O. Box 843015, Richmond, VA 23284-3015 (e-mail: jespeich{at}vcu.edu ) |
doi_str_mv | 10.1152/japplphysiol.00548.2006 |
format | Article |
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Submitted 15 May 2006
; accepted in final form 11 January 2007
Until the 1990s, the passive and active length-tension ( L -T) relationships of smooth muscle were believed to be static, with a single passive force value and a single maximum active force value for each muscle length. However, recent studies have demonstrated that the active L -T relationship in airway smooth muscle is dynamic and adapts to length changes over a period of time. Furthermore, our prior work showed that the passive L -T relationship in rabbit detrusor smooth muscle (DSM) is also dynamic and that in addition to viscoelastic behavior, DSM displays strain-softening behavior characterized by a loss of passive stiffness at shorter lengths following a stretch to a new longer length. This loss of passive stiffness appears to be irreversible when the muscle is not producing active force and during submaximal activation but is reversible on full muscle activation, which indicates that the stiffness component of passive force lost to strain softening is adjustable in DSM. The present study demonstrates that the passive L -T curve for DSM is not static and can shift along the length axis as a function of strain history and activation history. This study also demonstrates that adjustable passive stiffness (APS) can modulate total force (35% increase) for a given muscle length, while active force remains relatively unchanged (4% increase). This finding suggests that the structures responsible for APS act in parallel with the contractile apparatus, and the results are used to further justify the configuration of modeling elements within our previously proposed mechanical model for APS.
muscle mechanics; preconditioning; strain softening; passive force; active force
Address for reprint requests and other correspondence: J. E. Speich, Virginia Commonwealth Univ., Dept. of Mechanical Engineering, 601 West Main St., P.O. Box 843015, Richmond, VA 23284-3015 (e-mail: jespeich{at}vcu.edu )</description><identifier>ISSN: 8750-7587</identifier><identifier>EISSN: 1522-1601</identifier><identifier>DOI: 10.1152/japplphysiol.00548.2006</identifier><identifier>PMID: 17234807</identifier><identifier>CODEN: JAPHEV</identifier><language>eng</language><publisher>Bethesda, MD: Am Physiological Soc</publisher><subject>Anatomy & physiology ; Animals ; Biological and medical sciences ; Biomechanical Phenomena ; Cell Size ; Compliance ; Female ; Fundamental and applied biological sciences. Psychology ; In Vitro Techniques ; Lungs ; Models, Biological ; Muscle Contraction ; Muscle Proteins - physiology ; Muscle, Smooth - cytology ; Muscle, Smooth - physiology ; Muscular system ; Myocytes, Smooth Muscle - physiology ; Rabbits ; Reflex, Stretch ; Time Factors ; Urinary Bladder - physiology</subject><ispartof>Journal of applied physiology (1985), 2007-05, Vol.102 (5), p.1746-1755</ispartof><rights>2007 INIST-CNRS</rights><rights>Copyright American Physiological Society May 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c514t-62ce4b4562804c5a998f784f9be226163fc52577116ff7f2de3b613b277708e13</citedby><cites>FETCH-LOGICAL-c514t-62ce4b4562804c5a998f784f9be226163fc52577116ff7f2de3b613b277708e13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3026,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18748592$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17234807$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Speich, John E</creatorcontrib><creatorcontrib>Dosier, Christopher</creatorcontrib><creatorcontrib>Borgsmiller, Lindsey</creatorcontrib><creatorcontrib>Quintero, Kevin</creatorcontrib><creatorcontrib>Koo, Harry P</creatorcontrib><creatorcontrib>Ratz, Paul H</creatorcontrib><title>Adjustable passive length-tension curve in rabbit detrusor smooth muscle</title><title>Journal of applied physiology (1985)</title><addtitle>J Appl Physiol (1985)</addtitle><description>Departments of 1 Mechanical Engineering, 2 Biomedical Engineering, 3 Surgery, 4 Biochemistry, and 5 Pediatrics, Virginia Commonwealth University, Richmond, Virginia
Submitted 15 May 2006
; accepted in final form 11 January 2007
Until the 1990s, the passive and active length-tension ( L -T) relationships of smooth muscle were believed to be static, with a single passive force value and a single maximum active force value for each muscle length. However, recent studies have demonstrated that the active L -T relationship in airway smooth muscle is dynamic and adapts to length changes over a period of time. Furthermore, our prior work showed that the passive L -T relationship in rabbit detrusor smooth muscle (DSM) is also dynamic and that in addition to viscoelastic behavior, DSM displays strain-softening behavior characterized by a loss of passive stiffness at shorter lengths following a stretch to a new longer length. This loss of passive stiffness appears to be irreversible when the muscle is not producing active force and during submaximal activation but is reversible on full muscle activation, which indicates that the stiffness component of passive force lost to strain softening is adjustable in DSM. The present study demonstrates that the passive L -T curve for DSM is not static and can shift along the length axis as a function of strain history and activation history. This study also demonstrates that adjustable passive stiffness (APS) can modulate total force (35% increase) for a given muscle length, while active force remains relatively unchanged (4% increase). This finding suggests that the structures responsible for APS act in parallel with the contractile apparatus, and the results are used to further justify the configuration of modeling elements within our previously proposed mechanical model for APS.
muscle mechanics; preconditioning; strain softening; passive force; active force
Address for reprint requests and other correspondence: J. E. Speich, Virginia Commonwealth Univ., Dept. of Mechanical Engineering, 601 West Main St., P.O. Box 843015, Richmond, VA 23284-3015 (e-mail: jespeich{at}vcu.edu )</description><subject>Anatomy & physiology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biomechanical Phenomena</subject><subject>Cell Size</subject><subject>Compliance</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>In Vitro Techniques</subject><subject>Lungs</subject><subject>Models, Biological</subject><subject>Muscle Contraction</subject><subject>Muscle Proteins - physiology</subject><subject>Muscle, Smooth - cytology</subject><subject>Muscle, Smooth - physiology</subject><subject>Muscular system</subject><subject>Myocytes, Smooth Muscle - physiology</subject><subject>Rabbits</subject><subject>Reflex, Stretch</subject><subject>Time Factors</subject><subject>Urinary Bladder - physiology</subject><issn>8750-7587</issn><issn>1522-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kN1rFDEUxYNY7Fr9F3QQKvgwa5LJ1z6WYm2h4Et9DplMsjNLZjLmQ7v_vRl3YEXw6cK9v3PO5QDwHsEtQhR_Pqh5dnN_jIN3WwgpEVsMIXsBNuWKa8Qgegk2glNYcyr4JXgd4wFCRAhFr8Al4rghAvINuL_pDjkm1TpTzSrG4aepnJn2qa-TmYr9VOkcynKYqqDadkhVZ1LI0Ycqjt6nvhpz1M68ARdWuWjervMKfL_78nR7Xz9--_pwe_NYa4pIqhnWhrSEMiwg0VTtdsJyQeyuNRgzxBqrKaacI8Ss5RZ3pmkZalrMOYfCoOYKfDz5zsH_yCYmOQ5RG-fUZHyOkkPCIUe0gB_-AQ8-h6n8JjHGiBY7ViB-gnTwMQZj5RyGUYWjRFAuTcu_m5Z_mpZL00X5brXP7Wi6s26ttgDXK6CiVs4GNekhnjnBiaA7XLhPJ64f9v2vIRi5pvn9cUkvn2BJiy9ZQun_2bvs3JN5TovorJFzZ5vfOQirnA</recordid><startdate>20070501</startdate><enddate>20070501</enddate><creator>Speich, John E</creator><creator>Dosier, Christopher</creator><creator>Borgsmiller, Lindsey</creator><creator>Quintero, Kevin</creator><creator>Koo, Harry P</creator><creator>Ratz, Paul H</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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20070501</creationdate><title>Adjustable passive length-tension curve in rabbit detrusor smooth muscle</title><author>Speich, John E ; Dosier, Christopher ; Borgsmiller, Lindsey ; Quintero, Kevin ; Koo, Harry P ; Ratz, Paul H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c514t-62ce4b4562804c5a998f784f9be226163fc52577116ff7f2de3b613b277708e13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Anatomy & physiology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biomechanical Phenomena</topic><topic>Cell Size</topic><topic>Compliance</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>In Vitro Techniques</topic><topic>Lungs</topic><topic>Models, Biological</topic><topic>Muscle Contraction</topic><topic>Muscle Proteins - physiology</topic><topic>Muscle, Smooth - cytology</topic><topic>Muscle, Smooth - physiology</topic><topic>Muscular system</topic><topic>Myocytes, Smooth Muscle - physiology</topic><topic>Rabbits</topic><topic>Reflex, Stretch</topic><topic>Time Factors</topic><topic>Urinary Bladder - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Speich, John E</creatorcontrib><creatorcontrib>Dosier, Christopher</creatorcontrib><creatorcontrib>Borgsmiller, Lindsey</creatorcontrib><creatorcontrib>Quintero, Kevin</creatorcontrib><creatorcontrib>Koo, Harry P</creatorcontrib><creatorcontrib>Ratz, Paul H</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>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</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>Speich, John E</au><au>Dosier, Christopher</au><au>Borgsmiller, Lindsey</au><au>Quintero, Kevin</au><au>Koo, Harry P</au><au>Ratz, Paul H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adjustable passive length-tension curve in rabbit detrusor smooth muscle</atitle><jtitle>Journal of applied physiology (1985)</jtitle><addtitle>J Appl Physiol (1985)</addtitle><date>2007-05-01</date><risdate>2007</risdate><volume>102</volume><issue>5</issue><spage>1746</spage><epage>1755</epage><pages>1746-1755</pages><issn>8750-7587</issn><eissn>1522-1601</eissn><coden>JAPHEV</coden><abstract>Departments of 1 Mechanical Engineering, 2 Biomedical Engineering, 3 Surgery, 4 Biochemistry, and 5 Pediatrics, Virginia Commonwealth University, Richmond, Virginia
Submitted 15 May 2006
; accepted in final form 11 January 2007
Until the 1990s, the passive and active length-tension ( L -T) relationships of smooth muscle were believed to be static, with a single passive force value and a single maximum active force value for each muscle length. However, recent studies have demonstrated that the active L -T relationship in airway smooth muscle is dynamic and adapts to length changes over a period of time. Furthermore, our prior work showed that the passive L -T relationship in rabbit detrusor smooth muscle (DSM) is also dynamic and that in addition to viscoelastic behavior, DSM displays strain-softening behavior characterized by a loss of passive stiffness at shorter lengths following a stretch to a new longer length. This loss of passive stiffness appears to be irreversible when the muscle is not producing active force and during submaximal activation but is reversible on full muscle activation, which indicates that the stiffness component of passive force lost to strain softening is adjustable in DSM. The present study demonstrates that the passive L -T curve for DSM is not static and can shift along the length axis as a function of strain history and activation history. This study also demonstrates that adjustable passive stiffness (APS) can modulate total force (35% increase) for a given muscle length, while active force remains relatively unchanged (4% increase). This finding suggests that the structures responsible for APS act in parallel with the contractile apparatus, and the results are used to further justify the configuration of modeling elements within our previously proposed mechanical model for APS.
muscle mechanics; preconditioning; strain softening; passive force; active force
Address for reprint requests and other correspondence: J. E. Speich, Virginia Commonwealth Univ., Dept. of Mechanical Engineering, 601 West Main St., P.O. Box 843015, Richmond, VA 23284-3015 (e-mail: jespeich{at}vcu.edu )</abstract><cop>Bethesda, MD</cop><pub>Am Physiological Soc</pub><pmid>17234807</pmid><doi>10.1152/japplphysiol.00548.2006</doi><tpages>10</tpages></addata></record> |
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subjects | Anatomy & physiology Animals Biological and medical sciences Biomechanical Phenomena Cell Size Compliance Female Fundamental and applied biological sciences. Psychology In Vitro Techniques Lungs Models, Biological Muscle Contraction Muscle Proteins - physiology Muscle, Smooth - cytology Muscle, Smooth - physiology Muscular system Myocytes, Smooth Muscle - physiology Rabbits Reflex, Stretch Time Factors Urinary Bladder - physiology |
title | Adjustable passive length-tension curve in rabbit detrusor smooth muscle |
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