Literature DB >> 1593468

The stimulus interval-tension relation in enzymatically isolated single myocytes of the frog heart.

G Cecchi1, F Colomo, C Poggesi, C Tesi.   

Abstract

1. Apparatus for recording the small tensions developed by electrically stimulated single intact myocytes of frog heart is described. A laser-light optoelectronic transducer was used. The compliance of the force probes was 10-20 nm/nN, with a frequency response of 600-900 Hz in Ringer solution. The myocyte shortening during an ordinary twitch contraction was no greater than 1% of the slack length. The overall sensitivity of the transducer system was 5-10 mV/nN, with a total noise of 0.5-1 nN peak to peak. The experiments were performed at 20-23 degrees C on either atrial or ventricular myocytes at 2.15-2.2 microns sarcomere length, in 1 mM-Ca2+ Ringer solution. 2. Isoprenaline (5 microM), increases in external Ca2+ concentration ([Ca2+]o), and shortening of stimulus interval potentiated the myocyte twitch tension. The dependence of twitch characteristics on these inotropic interventions for all the atrial and ventricular myocytes tested was comparable to that of multicellular preparations under similar experimental conditions. This implies that the enzymatic isolation procedure had not altered the physiological properties of the myocytes. 3. The stimulus interval-tension relation for premature twitches of atrial and ventricular myocytes showed (i) a very steep rising phase in the region of intervals just longer than 0.52 and 0.66 s (the duration of the mechanical refractoriness in atrial or ventricular cells), (ii) a peak, at intervals of 0.7-0.8 s, where the twitch tension was strongly potentiated compared to that of the controls, and (iii) as the stimulus interval was further increased, a progressive return to the control level. The stimulus interval-tension relation for steady-state conditions exhibited similar characteristics. 4. The degree of tension potentiation by isoprenaline was greater in the controls than in the earliest test twitches. The result was that the stimulus interval-tension relations for isoprenaline-treated myocytes showed a gentler rise and a lower peak than for untreated cells. 5. The stimulus interval-tension relation of the heart is a basic property of its cells. It is related to changes in the activation level. The higher the activation level reached in control twitches, the lower the stimulus interval-dependent potentiation capability.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1593468      PMCID: PMC1176199          DOI: 10.1113/jphysiol.1992.sp019041

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  29 in total

Review 1.  THE INFLUENCE OF THE INTERVAL BETWEEN BEATS ON MYOCARDIAL CONTRACTILITY.

Authors:  J KOCH-WESER; J R BLINKS
Journal:  Pharmacol Rev       Date:  1963-09       Impact factor: 25.468

2.  [Dissociation of 2 factors: restitution & potentiation in the effect of the pause on the amplitude of myocardial contraction].

Authors:  P BRAVENY; V KRUTA
Journal:  Arch Int Physiol Biochim       Date:  1958-11

3.  A method for recording isometric tension development by isolated cardiac myocytes: transducer attachment with fibrin glue.

Authors:  L Copelas; M Briggs; W Grossman; J P Morgan
Journal:  Pflugers Arch       Date:  1987-03       Impact factor: 3.657

4.  Comparison of the effects of inotropic interventions on isometric tension and shortening in isolated ferret ventricular muscle.

Authors:  J A Lee; D G Allen
Journal:  Cardiovasc Res       Date:  1989-09       Impact factor: 10.787

5.  Receptor-controlled calcium discharge in frog heart cells.

Authors:  R Niedergerke; S Page
Journal:  Q J Exp Physiol       Date:  1989-12

Review 6.  Cellular mechanism of the relationship between myocardial force and frequency of contractions.

Authors:  B Lewartowski; B Pytkowski
Journal:  Prog Biophys Mol Biol       Date:  1987       Impact factor: 3.667

7.  A uniform enzymatic method for dissociation of myocytes from hearts and stomachs of vertebrates.

Authors:  R Mitra; M Morad
Journal:  Am J Physiol       Date:  1985-11

8.  Inactivation, reactivation and pacing dependence of calcium current in frog cardiocytes: correlation with current density.

Authors:  J A Argibay; R Fischmeister; H C Hartzell
Journal:  J Physiol       Date:  1988-07       Impact factor: 5.182

9.  High-speed ultrasensitive instrumentation for myofibril mechanics measurements.

Authors:  T Iwazumi
Journal:  Am J Physiol       Date:  1987-02

Review 10.  Mechanical properties of isolated cardiac myocytes.

Authors:  A J Brady
Journal:  Physiol Rev       Date:  1991-04       Impact factor: 37.312

View more
  5 in total

1.  A force transducer and a length-ramp generator for mechanical investigations of frog-heart myocytes.

Authors:  G Cecchi; F Colomo; C Poggesi; C Tesi
Journal:  Pflugers Arch       Date:  1993-04       Impact factor: 3.657

2.  Force regulation by Ca2+ in skinned single cardiac myocytes of frog.

Authors:  P W Brandt; F Colomo; N Piroddi; C Poggesi; C Tesi
Journal:  Biophys J       Date:  1998-04       Impact factor: 4.033

3.  Active and passive forces of isolated myofibrils from cardiac and fast skeletal muscle of the frog.

Authors:  F Colomo; N Piroddi; C Poggesi; G te Kronnie; C Tesi
Journal:  J Physiol       Date:  1997-04-15       Impact factor: 5.182

4.  Force responses to rapid length changes in single intact cells from frog heart.

Authors:  F Colomo; C Poggesi; C Tesi
Journal:  J Physiol       Date:  1994-03-01       Impact factor: 5.182

5.  Instrumentation to study myofibril mechanics from static to artificial simulations of cardiac cycle.

Authors:  Petr G Vikhorev; Michael A Ferenczi; Steven B Marston
Journal:  MethodsX       Date:  2016-03-02
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.