R. Kato et al., Fentanyl protects the heart against ischaemic injury via opioid receptors,adenosine A(1) receptors and K-ATP channel linked mechanisms in rats, BR J ANAEST, 84(2), 2000, pp. 204-214
Citations number
57
Categorie Soggetti
Aneshtesia & Intensive Care","Medical Research Diagnosis & Treatment
We have investigated if fentanyl protects against myocardial ischaemic inju
ry and if so, if the mechanism of this protection is mediated via opioid an
d adenosine A(1) receptors, and K-ATP channels. Langendorff rat hearts were
subjected to global ischaemia (30 min) and reperfusion (60 min). The drugs
were administered before induction of ischaemia and maintained throughout
the experiment. Treatment with fentanyl 740 nmol litre(-1) improved post-is
chaemic mechanical function, assessed as developed pressure, +dP/dtmax and
-dP/dtmin, compared with controls after 60 min of reperfusion. These effect
s were abolished by naloxone I mu mol litre(-1), DPCPX 10 mu mol litre(-1),
a selective adenosine A(1) antagonist and sodium 5-hydroxydecanoate 100 mu
mol litre(-1), a K-ATP(+) channel blocker. We conclude that fentanyl prote
cted the heart against post-ischaemic injury by a mechanism which was block
ed by an opioid and an adenosine A(1) receptor antagonist and also by a K-A
TP channel antagonist.