Literature DB >> 8010931

Effects of verapamil on myocardial stunning in xanthine-oxidase deficient hearts: pre-treatment vs. post-ischemic treatment.

T Adachi1, T Miura, K Suzuki, O Iimura.   

Abstract

The role of free radicals and the protective action of calcium antagonists have been established in myocardial stunning in canine hearts, which contain a considerable level of xanthine oxidase, a free radical producing enzyme. However, myocardial stunning in hearts which lack xanthine oxidase and its modification by calcium antagonists in vivo remain uncharacterized. The present study examined this issue using open-chest anesthetized rabbits. Myocardial stunning was induced by a 10-min coronary occlusion and reperfusion. Regional systolic thickening fraction (TF) was determined using an epicardial Doppler sensor, together with other hemodynamic parameters. In untreated control rabbits, recovery of TF from the 10 min transient ischemia was 43 +/- 3% of the baseline at 30 min after reperfusion. Administration of verapamil (200 micrograms/kg bolus plus 40 micrograms/kg/min), which was started before the onset of ischemia and continued until 20 min after reperfusion, significantly improved the recovery of TF to 74 +/- 6% (p < 0.05). A similar improvement in post-ischemic contractile function (TF = 77 +/- 10%) was observed when verapamil was injected at the same rate, but the infusion was discontinued 1 min after the coronary occlusion. Myocardial ATP depletion after the 10 min ischemia was significantly less in the verapamil-pretreated rabbits compared with untreated controls (10.1 +/- 1.0 vs. 6.2 +/- 0.7 mumol/g dry wt., p < 0.05). The difference in TF between the rabbit with and without verapamil treatment could not be explained by afterload reduction. When verapamil (100 micrograms/kg bolus plus 20 micrograms/kg/min) was given during the reperfusion period alone, TF recovery was poorer (TF = 22 +/- 8%) than the control value. Thus, it was concluded that verapamil attenuates myocardial stunning in the hearts with trace levels of xanthine oxidase, and that the beneficial effect is achieved only by pretreatment, not by post-ischemic treatment with verapamil.

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Year:  1994        PMID: 8010931     DOI: 10.1007/bf00788674

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


  33 in total

Review 1.  Myocardial stunning: a role for calcium antagonists during reperfusion?

Authors:  L Opie
Journal:  Cardiovasc Res       Date:  1992-01       Impact factor: 10.787

2.  Free radical-producing enzyme, xanthine oxidase, is undetectable in human hearts.

Authors:  L J Eddy; J R Stewart; H P Jones; T D Engerson; J M McCord; J M Downey
Journal:  Am J Physiol       Date:  1987-09

Review 3.  Xanthine oxidase: biochemistry, distribution and physiology.

Authors:  D A Parks; D N Granger
Journal:  Acta Physiol Scand Suppl       Date:  1986

4.  Validation of a single crystal for measurement of transmural and epicardial thickening.

Authors:  W X Zhu; M L Myers; C J Hartley; R Roberts; R Bolli
Journal:  Am J Physiol       Date:  1986-11

5.  Superoxide dismutase attenuated post-ischaemic contractile dysfunction in a myocardial xanthine oxidase deficient species.

Authors:  H Ooiwa; T Miura; T Iwamoto; T Ogawa; R Ishimoto; T Adachi; O Iimura
Journal:  Clin Exp Pharmacol Physiol       Date:  1992-02       Impact factor: 2.557

Review 6.  Mechanism of myocardial "stunning".

Authors:  R Bolli
Journal:  Circulation       Date:  1990-09       Impact factor: 29.690

7.  The calcium antagonist nisoldipine improves the functional recovery of reperfused myocardium only when given before ischemia.

Authors:  T Ehring; M Böhm; G Heusch
Journal:  J Cardiovasc Pharmacol       Date:  1992-07       Impact factor: 3.105

8.  Excitation-contraction coupling in postischemic myocardium. Does failure of activator Ca2+ transients underlie stunning?

Authors:  H Kusuoka; Y Koretsune; V P Chacko; M L Weisfeldt; E Marban
Journal:  Circ Res       Date:  1990-05       Impact factor: 17.367

9.  Xanthine oxidase as a source of free radical damage in myocardial ischemia.

Authors:  D E Chambers; D A Parks; G Patterson; R Roy; J M McCord; S Yoshida; L F Parmley; J M Downey
Journal:  J Mol Cell Cardiol       Date:  1985-02       Impact factor: 5.000

10.  Xanthine oxidase is not a source of free radicals in the ischemic rabbit heart.

Authors:  J M Downey; T Miura; L J Eddy; D E Chambers; T Mellert; D J Hearse; D M Yellon
Journal:  J Mol Cell Cardiol       Date:  1987-11       Impact factor: 5.000

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  1 in total

1.  Effects of 4'-chlorodiazepam on cellular excitation-contraction coupling and ischaemia-reperfusion injury in rabbit heart.

Authors:  David A Brown; Miguel A Aon; Fadi G Akar; Ting Liu; Nicolas Sorarrain; Brian O'Rourke
Journal:  Cardiovasc Res       Date:  2008-02-26       Impact factor: 10.787

  1 in total

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