Abstract |
Transient inhibition of gap junction (GJ)-mediated communication with heptanol during myocardial reperfusion limits infarct size. However, inhibition of cell coupling in normal myocardium may be arrhythmogenic. The purpose of this study was to test the hypothesis that the consequences of GJ inhibition may be magnified in reperfused myocardium compared with normal tissue, thus allowing the inhibition of GJs in reperfused tissue while only minimally modifying overall macroscopic cell coupling in normal myocardium. Concentration-response curves were defined for the effects of heptanol, 18alpha-glycyrrhetinic acid, halothane, and palmitoleic acid on conduction velocity, tissue electrical impedance, developed tension and lactate dehydrogenase (LDH) release in normoxically perfused rat hearts (n= 17). Concentrations lacking significant effects on tissue impedance were added during the initial 15 min of reperfusion in hearts submitted to 60 min (n= 43) or 30 min (n= 35) of ischaemia. These concentrations markedly increased myocardial electrical impedance (resistivity and phase angle) in myocardium reperfused after either 30 or 60 min of ischaemia, and reduced reperfusion-induced LDH release after 1 h of ischaemia by 83.6, 57.9, 51.7 and 52.5% for heptanol, 18alpha-glycyrrhetinic acid, halothane and palmitoleic acid, respectively. LDH release was minimal in hearts submitted to 30 min of ischaemia, independently of group allocation. In conclusion, the present results strongly support the hypothesis that intercellular communication in postischaemic myocardium may be effectively reduced by concentrations of GJ inhibitors affecting only minimally overall electrical impedance in normal myocardium. Reduction of cell coupling during initial reperfusion was consistently associated with attenuated lethal reperfusion injury.
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Authors | Antonio Rodriguez-Sinovas, David García-Dorado, Marisol Ruiz-Meana, Jordi Soler-Soler |
Journal | The Journal of physiology
(J Physiol)
Vol. 559
Issue Pt 1
Pg. 245-57
(Aug 15 2004)
ISSN: 0022-3751 [Print] England |
PMID | 15218064
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Uncoupling Agents
- Heptanol
- Halothane
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Topics |
- Action Potentials
(drug effects, physiology)
- Animals
- Dose-Response Relationship, Drug
- Gap Junctions
(drug effects, physiology)
- Halothane
(pharmacology)
- Heptanol
(pharmacology)
- Male
- Myocardial Reperfusion Injury
(metabolism)
- Myocardium
(metabolism)
- Rats
- Rats, Sprague-Dawley
- Uncoupling Agents
(pharmacology)
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