Literature DB >> 16051711

Depression of force production and ATPase activity in different types of human skeletal muscle fibers from patients with chronic heart failure.

P Szentesi1, M A Bekedam, B J van Beek-Harmsen, W J van der Laarse, R Zaremba, A Boonstra, F C Visser, G J M Stienen.   

Abstract

Isometric force production and ATPase activity were determined simultaneously in single human skeletal muscle fibers (n = 97) from five healthy volunteers and nine patients with chronic heart failure (CHF) at 20 degrees C. The fibers were permeabilized by means of Triton X-100 (1% vol/vol). ATPase activity was determined by enzymatic coupling of ATP resynthesis to the oxidation of NADH. Calcium-activated actomyosin (AM) ATPase activity was obtained by subtracting the activity measured in relaxing (pCa = 9) solutions from that obtained in maximally activating (pCa = 4.4) solutions. Fiber type was determined on the basis of myosin heavy chain isoform composition by polyacrylamide SDS gel electrophoresis. AM ATPase activity per liter cell volume (+/-SE) in the control and patient group, respectively, amounted to 134 +/- 24 and 77 +/- 9 microM/s in type I fibers (n = 11 and 16), 248 +/- 17 and 188 +/- 13 microM/s in type IIA fibers (n = 14 and 32), 291 +/- 29 and 126 +/- 21 microM/s in type IIA/X fibers (n = 3 and 5), and 325 +/- 32 and 205 +/- 21 microM/s in type IIX fibers (n = 7 and 9). The maximal isometric force per cross-sectional area amounted to 64 +/- 7 and 43 +/- 5 kN/m(2) in type I fibers, 86 +/- 11 and 58 +/- 4 kN/m(2) in type IIA fibers, 85 +/- 6 and 42 +/- 9 kN/m(2) in type IIA/X fibers, and 90 +/- 5 and 59 +/- 5 kN/m(2) in type IIX fibers in the control and patient group, respectively. These results indicate that, in CHF patients, significant reductions occur in isometric force and AM ATPase activity but that tension cost for each fiber type remains the same. This suggests that, in skeletal muscle from CHF patients, a decline in density of contractile proteins takes place and/or a reduction in the rate of cross-bridge attachment of approximately 30%, which exacerbates skeletal muscle weakness due to muscle atrophy.

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Year:  2005        PMID: 16051711     DOI: 10.1152/japplphysiol.00542.2005

Source DB:  PubMed          Journal:  J Appl Physiol (1985)        ISSN: 0161-7567


  22 in total

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2.  Chronic heart failure decreases cross-bridge kinetics in single skeletal muscle fibres from humans.

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Review 3.  Dietary Nitrate and Skeletal Muscle Contractile Function in Heart Failure.

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4.  Myosin heavy chain composition and the economy of contraction in healthy and diseased human myocardium.

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Journal:  J Muscle Res Cell Motil       Date:  2005-10-14       Impact factor: 2.698

5.  Myoglobin concentration in skeletal muscle fibers of chronic heart failure patients.

Authors:  Martijn A Bekedam; Brechje J van Beek-Harmsen; Willem van Mechelen; Anco Boonstra; Willem J van der Laarse
Journal:  J Appl Physiol (1985)       Date:  2009-08-06

6.  Skeletal muscle contractile protein function is preserved in human heart failure.

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Journal:  J Appl Physiol (1985)       Date:  2008-01-17

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Review 8.  Disease-Induced Skeletal Muscle Atrophy and Fatigue.

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9.  Reduced knee extensor function in heart failure is not explained by inactivity.

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Review 10.  Myofilament protein alterations promote physical disability in aging and disease.

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