{"title":"The force-calcium relationship is not affected by the cross-sectional area of skinned muscle fibres from rat soleus","authors":"Ian C. Smith , Venus Joumaa , Walter Herzog","doi":"10.1016/j.jbiomech.2025.112571","DOIUrl":null,"url":null,"abstract":"<div><div>Proportionality between force and muscle cross-sectional area (CSA) is a foundational principle in muscle mechanics. However, CSA-normalized force (known as specific force) is often lower in fibres with large CSAs compared to fibres with small CSAs from the same sample population. Many physiological mechanisms proposed to account for CSA-dependence of specific force converge on the requirement for fibre CSA to impact the relationship between force and the concentration of force-activating calcium. To determine if features of the force-calcium relationship exhibited CSA-dependence in mammalian skinned muscle fibres, force-calcium relationships were generated for 85 skinned slow soleus fibres of male Sprague-Dawley rats (<em>n</em> = 54 rats, 1–5 fibres per rat, age = 24 weeks, experimental temperature = 18 °C) and fit using the Hill equation. Fibres were separated into quartiles based on their CSA and then compared. Despite specific force being 46 % higher (<em>P</em> < 0.01) in the smallest (160 ± 51 mN∙mm<sup>−2</sup>; CSA = 3649 ± 708 μm<sup>2</sup>) compared to the largest (110 ± 20 mN∙mm<sup>−2</sup>; CSA = 8671 ± 1319 μm<sup>2</sup>) quartile, neither the calcium-sensitivity of force production (pCa50; <em>P</em> = 0.47; <em>F</em>(dFn = 3,DFd = 81) = 0.86) nor the Hill coefficient (<em>n<sub>H</sub></em>; <em>P</em> = 0.38; <em>F</em>(dFn = 3,DFd = 81) = 1.03) differed significantly between quartiles (smallest quartile: pCa50 = 6.015 ± 0.097, <em>n<sub>H</sub></em> = 1.80 ± 0.69; largest quartile: pCa50 = 6.062 ± 0.097, <em>n<sub>H</sub></em> = 1.63 ± 0.32). Force plateaus were observed at higher calcium concentrations in all fibres indicating that calcium was adequate for full activation. These findings add to the body of evidence suggesting that CSA-dependence of specific force in mammalian skinned fibres is an artifact attributable to the considerable imprecision associated with the assessment of fibre CSA, and not a physiological phenomenon which would require consideration when modeling muscle force output.</div></div>","PeriodicalId":15168,"journal":{"name":"Journal of biomechanics","volume":"182 ","pages":"Article 112571"},"PeriodicalIF":2.4000,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of biomechanics","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S002192902500082X","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
Proportionality between force and muscle cross-sectional area (CSA) is a foundational principle in muscle mechanics. However, CSA-normalized force (known as specific force) is often lower in fibres with large CSAs compared to fibres with small CSAs from the same sample population. Many physiological mechanisms proposed to account for CSA-dependence of specific force converge on the requirement for fibre CSA to impact the relationship between force and the concentration of force-activating calcium. To determine if features of the force-calcium relationship exhibited CSA-dependence in mammalian skinned muscle fibres, force-calcium relationships were generated for 85 skinned slow soleus fibres of male Sprague-Dawley rats (n = 54 rats, 1–5 fibres per rat, age = 24 weeks, experimental temperature = 18 °C) and fit using the Hill equation. Fibres were separated into quartiles based on their CSA and then compared. Despite specific force being 46 % higher (P < 0.01) in the smallest (160 ± 51 mN∙mm−2; CSA = 3649 ± 708 μm2) compared to the largest (110 ± 20 mN∙mm−2; CSA = 8671 ± 1319 μm2) quartile, neither the calcium-sensitivity of force production (pCa50; P = 0.47; F(dFn = 3,DFd = 81) = 0.86) nor the Hill coefficient (nH; P = 0.38; F(dFn = 3,DFd = 81) = 1.03) differed significantly between quartiles (smallest quartile: pCa50 = 6.015 ± 0.097, nH = 1.80 ± 0.69; largest quartile: pCa50 = 6.062 ± 0.097, nH = 1.63 ± 0.32). Force plateaus were observed at higher calcium concentrations in all fibres indicating that calcium was adequate for full activation. These findings add to the body of evidence suggesting that CSA-dependence of specific force in mammalian skinned fibres is an artifact attributable to the considerable imprecision associated with the assessment of fibre CSA, and not a physiological phenomenon which would require consideration when modeling muscle force output.
期刊介绍:
The Journal of Biomechanics publishes reports of original and substantial findings using the principles of mechanics to explore biological problems. Analytical, as well as experimental papers may be submitted, and the journal accepts original articles, surveys and perspective articles (usually by Editorial invitation only), book reviews and letters to the Editor. The criteria for acceptance of manuscripts include excellence, novelty, significance, clarity, conciseness and interest to the readership.
Papers published in the journal may cover a wide range of topics in biomechanics, including, but not limited to:
-Fundamental Topics - Biomechanics of the musculoskeletal, cardiovascular, and respiratory systems, mechanics of hard and soft tissues, biofluid mechanics, mechanics of prostheses and implant-tissue interfaces, mechanics of cells.
-Cardiovascular and Respiratory Biomechanics - Mechanics of blood-flow, air-flow, mechanics of the soft tissues, flow-tissue or flow-prosthesis interactions.
-Cell Biomechanics - Biomechanic analyses of cells, membranes and sub-cellular structures; the relationship of the mechanical environment to cell and tissue response.
-Dental Biomechanics - Design and analysis of dental tissues and prostheses, mechanics of chewing.
-Functional Tissue Engineering - The role of biomechanical factors in engineered tissue replacements and regenerative medicine.
-Injury Biomechanics - Mechanics of impact and trauma, dynamics of man-machine interaction.
-Molecular Biomechanics - Mechanical analyses of biomolecules.
-Orthopedic Biomechanics - Mechanics of fracture and fracture fixation, mechanics of implants and implant fixation, mechanics of bones and joints, wear of natural and artificial joints.
-Rehabilitation Biomechanics - Analyses of gait, mechanics of prosthetics and orthotics.
-Sports Biomechanics - Mechanical analyses of sports performance.