Literature DB >> 8974034

Excitation-contraction coupling of the developing rat heart.

M Vornanen1.   

Abstract

Postnatal maturation of rat heart is characterized by increases in force production, velocity of shortening and heart rate. Simultaneously with the enhanced cardiac power production the size of ventricular myocytes markedly increases. Parallel increase in cardiac rate functions and cells size would be expected to require reorganization of cardiac Ca regulation so that adequate rate of Ca release and uptake can be maintained. In accordance with this the source of activator Ca shifts from extracellular space to intracellular stores within the first four or five weeks of postnatal life. Calcium handling of sarcoplasmic reticulum and sarcolemma change in complementary manner so that diminishing sarcolemmal Ca transport is compensated with enhanced Ca release and sequestration by the sarcoplasmic reticulum during the early postnatal development of rat heart. These functional changes are partly due to reciprocal alterations in surface area of sarcolemma and sarcoplasmic reticulum, partly due to age-dependent changes in the expression of different transport systems and their kinetic properties.

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Year:  1996        PMID: 8974034     DOI: 10.1007/bf00408635

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  50 in total

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8.  Characterization of Ca(2+)-release channels in fetal and adult rat hearts.

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Journal:  Am J Physiol       Date:  1995-09

9.  Tension production and thin-filament protein isoforms in developing rat myocardium.

Authors:  P J Reiser; M V Westfall; S Schiaffino; R J Solaro
Journal:  Am J Physiol       Date:  1994-10

10.  Shortening velocity and myosin and myofibrillar ATPase activity related to myosin isoenzyme composition during postnatal development in rat myocardium.

Authors:  V Cappelli; R Bottinelli; C Poggesi; R Moggio; C Reggiani
Journal:  Circ Res       Date:  1989-08       Impact factor: 17.367

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8.  Regulation of mitochondrial contact sites in neonatal, juvenile and diabetic hearts.

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  8 in total

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