MECHANICAL AND METABOLIC RESPONSES TO EXTRACORPOREAL REGIONAL HYPOPERFUSION OF THE PORCINE HEART

Citation
R. Tukkie et al., MECHANICAL AND METABOLIC RESPONSES TO EXTRACORPOREAL REGIONAL HYPOPERFUSION OF THE PORCINE HEART, Cardioscience, 5(2), 1994, pp. 107-114
Citations number
22
Categorie Soggetti
Cardiac & Cardiovascular System
Journal title
ISSN journal
10155007
Volume
5
Issue
2
Year of publication
1994
Pages
107 - 114
Database
ISI
SICI code
1015-5007(1994)5:2<107:MAMRTE>2.0.ZU;2-5
Abstract
Controversy exists as to whether hibernating myocardium is ischemic (w ith evidence of lactate production and ATP breakdown) during sustained coronary hypoperfusion or whether the oxygen supply is balanced by th e oxygen requirements of contractile function. To investigate the mech anical and metabolic response to a moderate reduction in regional coro nary blood flow, selective coronary perfusion was performed by a carot id-coronary shunt using a small roller pump circuit in six pigs. Flow was reduced for 45 minutes to 40% of base line followed by 2 hours rep erfusion at normal blood flow. No hemodynamic changes occurred during flow reduction and reperfusion. Reduction of coronary blood flow to 40 % resulted in a reduction in wall motion to 40.8 +/- 6.1% of base line . Two hours of reperfusion resulted in myocardial stunning shown by pe rsistence of wall motion abnormalities (reduction to 64.6 +/- 6.0% of base line) without histologic and electron microscopic evidence of nec rosis. The metabolic response to hypoperfusion varied from nil to subs tantial, measured as nucleotide catabolism and lactate production. We found no correlation between the base line normoxic contractile state and the magnitude of ischemic metabolite efflux. The efflux of lactate , inosine and uridine did not correlate with wall motion at each time during coronary flow reduction. Initial contractile recovery correlate d with maximal lactate and uridine efflux during hypoperfusion. The re sults provide evidence that, in the in-vivo porcine myocardium, modera te coronary hypoperfusion can exist without metabolic evidence of isch emia.