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   <subfield code="a">Deficit in human muscle strength with cast immobilization: contribution of inorganic phosphate</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Neeti Pathare, Jennifer Stevens, Glenn Walter, Prithvi Shah, Arun Jayaraman, Susan Tillman, Mark Scarborough, C. Parker Gibbs, Krista Vandenborne]</subfield>
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   <subfield code="a">Metabolic factors have been proposed to explain strength deficits observed in skeletal muscle with immobilization that are not completely accounted for by changes in muscle cross-sectional area (CSA) and neural adaptations. The aim of this study was to quantify changes in the resting inorganic phosphate (Pi) concentration from the medial gastrocnemius muscle during immobilization, reloading and rehabilitation. Additionally, we assessed the contributions of CSA, muscle activation and Pi concentration to plantar flexor torque during rehabilitation following immobilization. Eight persons with a surgically stabilized ankle fracture participated. Subjects were immobilized for 6-8weeks and subsequently participated in 10weeks of rehabilitation. Localized 31P-Magnetic resonance spectroscopy, magnetic resonance imaging, isometric torque and activation testing were performed on the immobilized and uninvolved limbs. At 6weeks of immobilization, significant differences were noted between the immobilized and uninvolved limbs for the Pi concentration and the Pi/PCr ratio (P&lt;0.05). From 6weeks of immobilization to 3-5days of reloading, the increase in Pi concentration (15%, P=0.26) and Pi/PCr (20%, P=0.29) was not significant. During rehabilitation, the relative contributions of CSA, muscle activation and Pi concentration to plantarflexor torque were 32, 44 and 40%, respectively. Together, CSA, muscle activation and Pi concentration accounted for 76% of the variance in torque (P&lt;0.01). In summary, our findings suggest that immobilization, independent of reloading, leads to a significant increase in the resting Pi concentration of human skeletal muscle. Additionally, alterations in resting Pi concentration may contribute to strength deficits with immobilization not accounted for by changes in muscle CSA or neural adaptations.</subfield>
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   <subfield code="a">Springer-Verlag, 2006</subfield>
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   <subfield code="a">Immobilization</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Muscle strength</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Inorganic phosphate</subfield>
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   <subfield code="a">Muscle cross-sectional area</subfield>
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   <subfield code="a">Muscle activation</subfield>
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   <subfield code="a">Magnetic resonance</subfield>
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   <subfield code="a">Pathare</subfield>
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   <subfield code="u">Department of Physical Therapy, University of Florida, PO Box 100154, 32610, Gainesville, FL, USA</subfield>
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   <subfield code="a">Stevens</subfield>
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   <subfield code="u">Department of Physical Therapy, University of Florida, PO Box 100154, 32610, Gainesville, FL, USA</subfield>
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   <subfield code="a">Walter</subfield>
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   <subfield code="u">Department of Physiology and Functional Genomics, University of Florida, 32610, Gainesville, FL, USA</subfield>
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   <subfield code="u">Department of Physical Therapy, University of Florida, PO Box 100154, 32610, Gainesville, FL, USA</subfield>
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   <subfield code="a">Tillman</subfield>
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   <subfield code="a">Parker Gibbs</subfield>
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   <subfield code="u">Department of Physical Therapy, University of Florida, PO Box 100154, 32610, Gainesville, FL, USA</subfield>
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   <subfield code="t">European Journal of Applied Physiology</subfield>
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   <subfield code="g">98/1(2006-09-01), 71-78</subfield>
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