Relation between ischemic preconditioning and the duration of sustained ischemia.
10.3346/jkms.1995.10.2.121
- Author:
Dae Joong KIM
1
;
Hyun KIM
;
Ji In PARK
;
Tae Sub SHIM
;
Bong Jin RAH
;
Ho Dirk KIM
Author Information
1. Department of Histology, College of Medicine, Chung-Ang University, Seoul, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- MeSH:
Animal;
Arrhythmia/prevention & control;
Calcium/metabolism;
Extracellular Space/metabolism;
Female;
Heart/physiology;
Hydrogen-Ion Concentration;
Male;
Myocardial Infarction/prevention & control;
Myocardial Ischemia/metabolism/*physiopathology;
Myocardial Reperfusion Injury/*prevention & control;
Myocardium/metabolism/pathology/ultrastructure;
Necrosis;
Rabbits;
Support, Non-U.S. Gov't;
Time Factors;
Ventricular Function, Left/physiology
- From:Journal of Korean Medical Science
1995;10(2):121-131
- CountryRepublic of Korea
- Language:English
-
Abstract:
It has been reported that repetitive brief periods of ischemia and reperfusion (ischemic preconditioning, IP) cause a significant reduction in the extent of myocardial necrosis or in the incidence of reperfusion arrhythmias in rat heart. However, recent reports have stated that IP effect is diminished or lost in the canine or bovine heart if ischemia (mostly regional) is sustained for 40 min or longer. The main objective of this study is to assess whether IP provides myocardial protection in prolonged sustained ischemia under the condition of global ischemia in isolated rabbit heart. The hearts were subjected to 10-60 min sustained ischemia (SI) followed by 60 min reperfusion with (IP heart) or without IP (ISCH heart). IP was induced by 4 cycles of 5 min global ischemia and 5 min reperfusion. Left ventricular function (LVF), extent of infarction (EI) and ultrastructural changes were examined. As a whole, the LVF began to recover on reperfusion but there was no significant difference in the functional parameters. However, extracellular Ca2+ concentration was lower in the ISCH hearts (p <0.05) and the EI was significantly different between the hearts which had received 60 min SI (67% in the ISCH versus 32% in the IP heart, p <0.01). Ultrastructural changes were homogeneous in the ISCH hearts and became irreversible in accordance with increase of the duration of ischemia, while these changes were heterogeneous and restricted in the IP heart. These results suggest that IP does not attenuate the postischemic dysfunction in prolonged ischemia but it can provide an infarct size-limiting effect and delay ultrastructural changes. This cardioprotective effect may be related to calcium homeostasis.
