Duration of ischaemia determines matrix metalloproteinase-2 activation in the reperfused rabbit heart

• Published in: Proteomics (Weinheim) 2002-09, Vol.2 (9), p.1204-1210
• Main Authors: Prasan, Ananth M., McCarron, Hugh C. K., White, Melanie Y., McLennan, Susan V., Tchen, Adrian S., Hambly, Brett D., Jeremy, Richmond W.
• Format: Article
• Language: English
• Subjects: Animals; Enzyme Activation; Female; Hemodynamics; Ischemia; Male; Matrix Metalloproteinase 2 - metabolism; Matrix metalloproteinase-2; Myocardium - enzymology; Rabbit; Rabbits; Reperfusion; Reperfusion injury; Reverse Transcriptase Polymerase Chain Reaction; Stunned myocardium; Time Factors
• ISSN: 1615-9853; 1615-9861
• DOI: 10.1002/1615-9861(200209)2:9<1204::AID-PROT1204>3.0.CO;2-K

It has been hypothesised that activation of matrix metalloproteinase‐2 (MMP‐2) contributes to reversible myocardial dysfunction (stunning) following short‐term ischaemia and reperfusion. Gelatin zymography was used to measure release of both pro‐MMP‐2 (72 kDa) and MMP‐2 (62 kDa), into the coronary effluent from isolated, perfused rabbit hearts during 90 min aerobic perfusion (control), or low‐flow ischaemia (15 or 60 min at 1 mL/min), followed by 60 min reperfusion. In controls, pro‐MMP‐2 was detected in the coronary effluent throughout the first 30 min of aerobic perfusion, but MMP‐2 was not detected. In contrast, MMP‐2 was detected in the coronary effluent during reperfusion after both 15 and 60 min ischaemia. However, while left ventricular systolic function was impaired after both 15 min and 60 min ischaemia, a significant increase in the release of MMP‐2 was only detected in hearts following 60 min ischaemia. The dissociation between mechanical function and MMP‐2 levels suggest that MMP‐2 does not contribute to myocardial stunning in this model, but may contribute to myocardial dysfunction following prolonged ischaemia.