Ischemic reperfused heart represents a potential target for gene therapy be
cause gene transfer can represent an alternate pharmacological approach to
protect the heart from cellular injury. Gene therapy may be particularly us
eful to deal with previously unapproachable problems. For myocardial preser
vation, gene therapy could replace those pharmacological interventions when
drugs are delivered locally by sustained release with the help of mechanic
al device, eg, implants. In this review, attempts are made to define the mo
lecular targets for gene therapy primarily applicable to myocardial preserv
ation associated with ischemia and reperfusion. It has been emphasized that
for successful gene transfer, not only characterization of proper targets
and elimination of undesirable side effects are necessary, but also the the
rapy must be proven superior compared to other pharmacological intervention
s including surgery. (C) 1999 by The Society of Thoracic Surgeons.