Literature DB >> 8789377

Alterations in the force-frequency relationship by tert-butylbenzohydroquinone, a putative SR Ca2+ pump inhibitor, in rabbit and rat ventricular muscle.

S Baudet1, E Do, J Noireaud, H Le Marec.   

Abstract

1. The effects of 2,5 di-(tert-butyl)-1,4-benzohydroquinone (TBQ), a putative inhibitor of the sarcoplasmic reticulum (SR) Ca2+ pump, on twitch tension, time course and SR Ca2+ content have been studied at different stimulation frequencies (0.5-3 Hz) in isolated preparations from the rabbit and rat right ventricle, at 37 degrees C. 2. At 0.5Hz, 30 microM TBQ induced a marked negative inotropic effect in both species (-57% in the rabbit and -68% in the rat) and decreased the rate of rise and fall of twitch tension. In parallel, SR Ca2+ content (assessed by rapid cooling contractures) was depressed in the rabbit by 42%. The force-frequency relationship (positive for the rabbit and negative for the rat) was significantly attenuated. In the rabbit, this alteration was shown to rely on insufficient SR Ca2+ reloading with increasing frequencies. 3. Exposure of TBQ-treated preparations to 8 mM extracellular Ca2+ or 5 microM isoprenaline were effective in reloading the SR with Ca2+ whereas 20 mM caffeine emptied this compartment. 4. In the rabbit ventricle, increase in stimulation frequency shortened control twitch time course by decreasing both the time to peak tension (TTP) and the time to half relaxation (t1/2). TBQ did not differentially affect the pattern for t1/2 but significantly attenuated the frequency-induced decrease of TTP. 5. In rabbit ventricular muscle, the action potential duration increased between 0.5 and 3 Hz whether or not TBQ was present. However, TBQ induced a small but significant additional action potential shortening. 6. TBQ decreased twitch tension in the rat ventricle between 0.5 and 3 Hz but the negative staircase was not differentially affected by the SR Ca2+ pump inhibitor. In control conditions and in the presence of 30 microM TBQ, t1/2 was frequency-independent but TBQ consistently increased this parameter (by approximately 29%). 7. These data argue in favour of a specific and partial inhibition of the SR Ca2+ pump by 30 microM TBQ in the rabbit and rat ventricle and emphasise the importance of SR Ca2+ uptake in the force-frequency phenomenon.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8789377      PMCID: PMC1909275          DOI: 10.1111/j.1476-5381.1996.tb15185.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  40 in total

1.  Relationship between inotropy and relaxation in rat myocardium.

Authors:  D Chemla; Y Lecarpentier; J L Martin; M Clergue; A Antonetti; P Y Hatt
Journal:  Am J Physiol       Date:  1986-06

Review 2.  Specific inhibitors of intracellular Ca2+ transport ATPases.

Authors:  G Inesi; Y Sagara
Journal:  J Membr Biol       Date:  1994-07       Impact factor: 1.843

3.  Alterations of the force-frequency relation depending on stages of heart failure in humans.

Authors:  U Schmidt; R H Schwinger; M Böhm; E Erdmann
Journal:  Am J Cardiol       Date:  1994-11-15       Impact factor: 2.778

4.  Effects of thapsigargin and cyclopiazonic acid on the sarcoplasmic reticulum Ca2+ pump of skinned fibres from frog skeletal muscle.

Authors:  G G Du; C C Ashley; T J Lea
Journal:  Pflugers Arch       Date:  1994-12       Impact factor: 3.657

5.  Effect of cyclopiazonic acid, an inhibitor of sarcoplasmic reticulum Ca(2+)-ATPase, on the frequency-dependence of the contraction-relaxation cycle of the guinea-pig isolated atrium.

Authors:  N J Yard; M Chiesi; H A Ball
Journal:  Br J Pharmacol       Date:  1994-11       Impact factor: 8.739

6.  Influence of a change in stimulation rate on action potentials, currents and contractions in rat ventricular cells.

Authors:  M R Mitchell; T Powell; D A Terrar; V W Twist
Journal:  J Physiol       Date:  1985-07       Impact factor: 5.182

7.  Gene expression of the cardiac Na(+)-Ca2+ exchanger in end-stage human heart failure.

Authors:  R Studer; H Reinecke; J Bilger; T Eschenhagen; M Böhm; G Hasenfuss; H Just; J Holtz; H Drexler
Journal:  Circ Res       Date:  1994-09       Impact factor: 17.367

8.  CaMKII is responsible for activity-dependent acceleration of relaxation in rat ventricular myocytes.

Authors:  R A Bassani; A Mattiazzi; D M Bers
Journal:  Am J Physiol       Date:  1995-02

9.  Inhibition of L-type calcium-channel activity by thapsigargin and 2,5-t-butylhydroquinone, but not by cyclopiazonic acid.

Authors:  E J Nelson; C C Li; R Bangalore; T Benson; R S Kass; P M Hinkle
Journal:  Biochem J       Date:  1994-08-15       Impact factor: 3.857

10.  The relationship between contractile force and intracellular [Ca2+] in intact rat cardiac trabeculae.

Authors:  P H Backx; W D Gao; M D Azan-Backx; E Marban
Journal:  J Gen Physiol       Date:  1995-01       Impact factor: 4.086

View more
  2 in total

1.  Mechanisms underlying the frequency dependence of contraction and [Ca(2+)](i) transients in mouse ventricular myocytes.

Authors:  Gudrun Antoons; Kanigula Mubagwa; Ines Nevelsteen; Karin R Sipido
Journal:  J Physiol       Date:  2002-09-15       Impact factor: 5.182

2.  Endocardial endothelium is a key determinant of force-frequency relationship in rat ventricular myocardium.

Authors:  Xiaoxu Shen; Zhen Tan; Xin Zhong; Ye Tian; Xian Wang; Bo Yu; Genaro Ramirez-Correa; Anne Murphy; Kathleen Gabrielson; Nazareno Paolocci; Wei Dong Gao
Journal:  J Appl Physiol (1985)       Date:  2013-05-23
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.