Literature DB >> 9833153

Frequency dependent force generation correlates with sarcoplasmic calcium ATPase activity in human myocardium.

K Frank1, B Bölck, U Bavendiek, R H Schwinger.   

Abstract

OBJECTIVE: In congestive heart failure both a decreased function of the sarcoplasmic Ca(2+)-ATPase and a negative force-frequency relationship have been shown. This study aimed to investigate a possible relationship between frequency potentiation, sarcoplasmic Ca(2+)-ATPase activity, and SERCA2 protein expression in human myocardium.
METHODS: Frequency potentiation was studied in electrically stimulated, isometric, left ventricular papillary muscle strip preparations (37 degrees C, 0.5-3.0 Hz) from terminally failing (NYHA i.v.; n = 5, dilated cardiomyopathy) and nonfailing (donor hearts, n = 5) human myocardium. In the identical samples the Ca(2+)-ATPase activity (NADH coupled assay) and the protein expression of sarcoplasmic Ca(2+)-ATPase (SERCA2), phospholamban, and calsequestrin (western blot) were determined. The frequency dependent change in the force of contraction and Vmax of the Ca(2+)-ATPase activity and the protein expression of SERCA2 were correlated with each other.
RESULTS: In terminally failing myocardium the force-frequency relationship was negative (2.0 Hz vs. 0.5 Hz: -0.2 +/- 0.1 delta mN) contrasting a positive rate dependent potentiation of force in nonfailing tissue (2.0 Hz vs. 0.5 Hz: +0.8 +/- 0.2 delta mN; p < 0.01). In failing myocardium the corresponding maximal sarcoplasmic Ca(2+)-ATPase activity (Vmax) was reduced significantly compared to nonfailing myocardium (174 +/- 24 vs. 296 +/- 31 nmol ATP/mg.min, p < 0.01). The protein expression of SERCA2, phospholamban, and calsequestrin remained unchanged in failing myocardium. The maximal Ca(2+)-ATPase activity significantly correlated with the frequency dependent change in force of contraction (2 Hz vs. 0.5 Hz: r = 0.88, p = 0.001; 3 Hz vs. 0.5 Hz: r = 0.84, p = 0.004). No correlation between protein expression of SERCA2 and Ca(2+)-ATPase activity or change in force of contraction was observed.
CONCLUSION: Due to a significant correlation between sarcoplasmic Ca(2+)-ATPase activity and frequency potentiation, the negative rate dependent force potentiation in human heart failure could be at least in part be attributed to decreased function of the sarcoplasmic Ca(2+)-ATPase.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9833153     DOI: 10.1007/s003950050109

Source DB:  PubMed          Journal:  Basic Res Cardiol        ISSN: 0300-8428            Impact factor:   17.165


  9 in total

1.  Transmural heterogeneity and remodeling of ventricular excitation-contraction coupling in human heart failure.

Authors:  Qing Lou; Vadim V Fedorov; Alexey V Glukhov; Nader Moazami; Vladimir G Fast; Igor R Efimov
Journal:  Circulation       Date:  2011-04-18       Impact factor: 29.690

2.  Effects of stimulation frequency versus pulse duration modulation on muscle fatigue.

Authors:  Trisha Kesar; Li-Wei Chou; Stuart A Binder-Macleod
Journal:  J Electromyogr Kinesiol       Date:  2007-02-21       Impact factor: 2.368

3.  Heterozygous SOD2 deletion selectively impairs SERCA function in the soleus of female mice.

Authors:  Jessica L Braun; Holt N Messner; Riley E G Cleverdon; Ryan W Baranowski; Sophie I Hamstra; Mia S Geromella; Jeffrey A Stuart; Val A Fajardo
Journal:  Physiol Rep       Date:  2022-05

4.  Posttranslational modifications of calcium/calmodulin-dependent protein kinase IIδ and its downstream signaling in human failing hearts.

Authors:  Tomas Rajtik; Eva Goncalvesova; Zoltan V Varga; Przemyslaw Leszek; Mariusz Kusmierczyk; Michal Hulman; Jan Kyselovic; Peter Ferdinandy; Adriana Adameova
Journal:  Am J Transl Res       Date:  2017-08-15       Impact factor: 4.060

Review 5.  Electrophysiological remodeling in heart failure.

Authors:  Yanggan Wang; Joseph A Hill
Journal:  J Mol Cell Cardiol       Date:  2010-01-20       Impact factor: 5.000

6.  Using customized rate-coding and recruitment strategies to maintain forces during repetitive activation of human muscles.

Authors:  Li-Wei Chou; Trisha M Kesar; Stuart A Binder-Macleod
Journal:  Phys Ther       Date:  2008-01-03

7.  SERCA2a tyrosine nitration coincides with impairments in maximal SERCA activity in left ventricles from tafazzin-deficient mice.

Authors:  Jessica L Braun; Sophie I Hamstra; Holt N Messner; Val A Fajardo
Journal:  Physiol Rep       Date:  2019-08

8.  Physiological calcium combined with electrical pacing accelerates maturation of human engineered heart tissue.

Authors:  Shi Shen; Lorenzo R Sewanan; Stephanie Shao; Saiti S Halder; Paul Stankey; Xia Li; Stuart G Campbell
Journal:  Stem Cell Reports       Date:  2022-08-04       Impact factor: 7.294

9.  Increased SERCA2a sub-cellular heterogeneity in right-ventricular heart failure inhibits excitation-contraction coupling and modulates arrhythmogenic dynamics.

Authors:  M Holmes; M E Hurley; T M D Sheard; A P Benson; I Jayasinghe; M A Colman
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2022-10-03       Impact factor: 6.671

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.