Literature DB >> 7494541

Adaptation of the heart to ischemia by preconditioning: effects on energy equilibrium, properties of sarcolemmal ATPases and release of cardioprotective proteins.

A Ziegelhöffer1, N Vrbjar, J Styk, A Breier, A Dzurba, T Ravingerová.   

Abstract

Ischemic preconditioning of the heart is referred as a manifest increase in tolerance of the myocardium to otherwise damaging ischemic insult, achieved by one or few consequent initial short exposures to ischemia, each followed by reperfusion of the ischemic area. Several mechanisms such as opening of collateral vessels, the action of catecholamines, inositol phosphates, G-proteins and/or adenosine; inhibition of mitochondrial ATPase, the effects of different endogenous protective substances like heat stress or shock proteins, etc., are believed to cooperate in the mechanism of induction of preconditioning or in maintaining its effect. The present study is an attempt to extend the present knowledge about preconditioning from two aspects: i.) the peculiarities of energy equilibrium in preconditioned myocardium including adaptation of cardiac sarcolemmal ATPases to ischemia and/or hypoxia, and ii) participation of a new endogenous cardioprotective substance in the mechanism of preconditioning. The energy equilibrium in preconditioning is characterized by adaptation of cardiac energy demands to the capacity of energy production and delivery decreased by anaerobiosis and is manifested by constant ratios between ATP, ADP, AMP and the sum of ADN. Principles are proposed that may enable a prediction and mathematical modelling of the balanced energetic state in the preconditioned myocardium. These principles are based on thermodynamics and involve besides others a more economic handling of ATP by sarcolemmal ATPases. The latter enzymes adapt themselves to lowered availability of ATP by decreasing besides their Vmax also their values of Km (increase in the affinity) for ATP and some of them even adjust their activation energy (the anaerobiosis-induced elevation of Ea.t. is missing).(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1995        PMID: 7494541     DOI: 10.1007/bf00944793

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


  30 in total

1.  A microcolorimetric method for the determination of inorganic phosphorus.

Authors:  H H TAUSSKY; E SHORR
Journal:  J Biol Chem       Date:  1953-06       Impact factor: 5.157

2.  Features of the (Na, K)-ATPase of cardiac sarcolemma with particular reference to myocardial ischaemia.

Authors:  N Vrbjar; J Slezak; A Ziegelhoffer; N Tribulova
Journal:  Eur Heart J       Date:  1991-12       Impact factor: 29.983

3.  Increased affinity to substrate in sarcolemmal ATPases from hearts acclimatized to high altitude hypoxia.

Authors:  A Ziegelhöffer; J Procházka; V Pelouch; B Ostádal; A Dzurba; N Vrbjar
Journal:  Physiol Bohemoslov       Date:  1987

4.  Enzyme kinetics and the activation energy of (Na,K)-ATPase in ischaemic hearts: influence of the duration of ischaemia.

Authors:  N Vrbjar; A Dzurba; A Ziegelhöffer
Journal:  Gen Physiol Biophys       Date:  1994-10       Impact factor: 1.512

5.  Repetitive episodes of brief ischaemia (12 min) do not produce a cumulative depletion of high energy phosphate compounds.

Authors:  J L Swain; R L Sabina; J J Hines; J C Greenfield; E W Holmes
Journal:  Cardiovasc Res       Date:  1984-05       Impact factor: 10.787

6.  Adaptation to ischemia during percutaneous transluminal coronary angioplasty. Clinical, hemodynamic, and metabolic features.

Authors:  E Deutsch; M Berger; W G Kussmaul; J W Hirshfeld; H C Herrmann; W K Laskey
Journal:  Circulation       Date:  1990-12       Impact factor: 29.690

7.  Protective effects of preconditioning of the ischaemic myocardium involve cyclo-oxygenase products.

Authors:  A Vegh; L Szekeres; J R Parratt
Journal:  Cardiovasc Res       Date:  1990-12       Impact factor: 10.787

8.  Cardiac stress protein elevation 24 hours after brief ischemia or heat stress is associated with resistance to myocardial infarction.

Authors:  M S Marber; D S Latchman; J M Walker; D M Yellon
Journal:  Circulation       Date:  1993-09       Impact factor: 29.690

9.  Blockade of ATP-sensitive potassium channels prevents myocardial preconditioning in dogs.

Authors:  G J Gross; J A Auchampach
Journal:  Circ Res       Date:  1992-02       Impact factor: 17.367

10.  Evaluation of ischemia-reperfusion injury by malondialdehyde, glutathione and gamma-glutamyl transpeptidase: lack of specific local effects in diverse parts of the dog heart following acute coronary occlusion.

Authors:  O Ondrejickova; A Ziegelhoeffer; I Gabauer; R Sotnikova; J Styk; P Gibala; J Sedlak; L Horakova
Journal:  Cardioscience       Date:  1993-12
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