Literature DB >> 7702545

Involvement of ATP-sensitive potassium channels in preconditioning protection.

S Rohmann1, H Weygandt, P Schelling, L Kie Soei, P D Verdouw, I Lues.   

Abstract

Single or multiple brief periods of ischemia (preconditioning, PC) have been shown to protect the myocardium from infarction during a subsequent more prolonged ischemic insult. To test the hypothesis that opening of ATP-sensitive potassium channels (KATP) is involved in this mechanism, either bimakalim, a KATP channel opener, or glibenclamide, a KATP channel blocker, were administered to mimic or to block preconditioning protection in barbital-anesthetized pigs. PC was elicited by a single period of 10 min left anterior descending coronary artery (LADCA) occlusion followed by 15 min of reperfusion before the LADCA was reoccluded for 60 min. Instead of PC, bimakalim infusion was started 15 min before the 60 min LADCA occlusion (TCO) and stopped with the onset of ischemia. Glibenclamide was administered either for 10 min prior to the PC protocol, before bimakalim infusion, or before TCO. Regional wall function was quantified with ultrasonic crystals aligned to measure wall thickening (% delta WT). At the end of the protocol, infarct size was determined by incubating myocardium with p-nitrobluetetrazolium. In seven preconditioned pigs, infarct size was 9.9 +/- 5.1% of the risk region compared with 65.9 +/- 6.0% in the seven control pigs subjected to 60 min of ischemia only (p < 0.001). In seven pigs treated with bimakalim, infarct size was reduced to 35.3 +/- 6.6 (p < 0.05 vs. controls). Blocking ATP-sensitive potassium channels with glibenclamide prior to PC abolished its protective effect (infarct size, 62.2 +/- 4.5%; p < 0.001 vs. PC alone). Glibenclamide also antagonized the protective effect of bimakalim (infarct size, 55.2 +/- 4.0%), but did not affect infarct size, when solely administered prior to the prolonged ischemic period (62.2 +/- 4.3%). We conclude that in swine myocardium KATP channels are involved in the protective effect of ischemic preconditioning, since glibenclamide completely abolished the protective effect of preconditioning, while bimakalim could--at least in part--mimic it.

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Year:  1994        PMID: 7702545     DOI: 10.1007/bf00794956

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


  33 in total

Review 1.  Influence of myocardial ischemia and infarction on autonomic innervation of heart.

Authors:  D P Zipes
Journal:  Circulation       Date:  1990-10       Impact factor: 29.690

2.  Origin of anterior interventricular vein blood in domestic swine.

Authors:  J Bier; B Sharaf; H Gewirtz
Journal:  Am J Physiol       Date:  1991-05

Review 3.  Adenosine triphosphate-sensitive potassium channels in the cardiovascular system.

Authors:  C G Nichols; W J Lederer
Journal:  Am J Physiol       Date:  1991-12

4.  An explanation for the reported observation that ATP dependent potassium channel openers mimic preconditioning.

Authors:  J M Downey
Journal:  Cardiovasc Res       Date:  1993-09       Impact factor: 10.787

5.  Limitation of infarct size in the rabbit by ischaemic preconditioning is reversible with glibenclamide.

Authors:  C F Toombs; T L Moore; R J Shebuski
Journal:  Cardiovasc Res       Date:  1993-04       Impact factor: 10.787

6.  Myocardial lactate extraction: multi-determined metabolic function.

Authors:  E W Gertz; J A Wisneski; R Neese; A Houser; R Korte; J D Bristow
Journal:  Circulation       Date:  1980-02       Impact factor: 29.690

7.  Blockade of ATP-sensitive potassium channels increases infarct size but does not prevent preconditioning in rabbit hearts.

Authors:  J D Thornton; C S Thornton; D L Sterling; J M Downey
Journal:  Circ Res       Date:  1993-01       Impact factor: 17.367

8.  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

9.  Ischemic preconditioning protects against infarction in rat heart.

Authors:  Y Liu; J M Downey
Journal:  Am J Physiol       Date:  1992-10

10.  Myocardial protection with preconditioning.

Authors:  G C Li; J A Vasquez; K P Gallagher; B R Lucchesi
Journal:  Circulation       Date:  1990-08       Impact factor: 29.690

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  3 in total

1.  Blockade of the KATP-channel by glibenclamide aggravates ischemic injury, and counteracts ischemic preconditioning.

Authors:  J Munch-Ellingsen; E Bugge; K Ytrehus
Journal:  Basic Res Cardiol       Date:  1996 Sep-Oct       Impact factor: 17.165

2.  Monophosphoryl Lipid A: A Novel Agent for Inducing Pharmacologic Myocardial Preconditioning.

Authors: 
Journal:  J Thromb Thrombolysis       Date:  1996       Impact factor: 2.300

3.  Cardioprotection associated with preconditioning in the anesthetized ferret.

Authors:  A W Gomoll
Journal:  Basic Res Cardiol       Date:  1996 Nov-Dec       Impact factor: 17.165

  3 in total

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