THE REINTRODUCTION OF ISCHEMIC PRECONDITIONING IS ABLE TO PROTECT MYOCARDIUM AFTER REPEATED LONG REPERFUSION INTERVALS

Citation
Ek. Iliodromitis et al., THE REINTRODUCTION OF ISCHEMIC PRECONDITIONING IS ABLE TO PROTECT MYOCARDIUM AFTER REPEATED LONG REPERFUSION INTERVALS, Cardioscience, 5(4), 1994, pp. 277-281
Citations number
13
Categorie Soggetti
Cardiac & Cardiovascular System
Journal title
ISSN journal
10155007
Volume
5
Issue
4
Year of publication
1994
Pages
277 - 281
Database
ISI
SICI code
1015-5007(1994)5:4<277:TROIPI>2.0.ZU;2-E
Abstract
Classic ischemic preconditioning confers protection to the vulnerable myocardium following brief periods of ischemia with short intermittent periods of reperfusion. The aims of this study were: (i) to ascertain the protection from preconditioning using a relatively long reperfusi on interval; (ii) to see whether this protection exists if preconditio ning and long reperfusion is repeated and (iii) to evaluate the effect that an additional preconditioning stimulus has if it is given immedi ately before the sustained ischemia. Following anesthesia, in-vivo hea rts were preconditioned with a 5 minute coronary ligation followed by 10 minutes reperfusion (Group A). This was compared to groups that wer e preconditioned with 5 minutes ischemia and 1 hour reperfusion (Group B); or 5 minutes ischemia with 1 hour reperfusion, repeated twice (Gr oup C); or 5 minutes ischemic with 1 hour reperfusion repeated twice a nd followed by 5 minutes ischemia and 10 minutes reperfusion (Group D) . Protection was assessed by subjecting each of the above groups to a further 45 minutes of regional ischemia followed by 120 minutes reperf usion. This protocol without prior preconditioning served as a control (Group E). The ratio of the infarcted to risk area was 23.1+/-4.1% in group A, 38.3+/-3.5% in group B, 58.4+/-4.9% in group C, 10.4+/-3.1% in group D and 61.8+/-6.2% in the control group E. Group D was signifi cantly different from all the other groups. Group B was not different in comparison to the control group E. When a relatively long reperfusi on period (Group B) was introduced the preconditioning protection dimi nished. When this long reperfusion period was repeated (Group C) overa ll protection was lost. However, when preconditioning was re-introduce d alter a long delay (Group D), the protection afforded by it not only returned but appeared to be potentiated.