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Remifentanilandcardiacpreconditioning
MichaelGIrwin,UniversityofHongKong
Cardiacpreconditioningrepresentsthemostpotentandconsistentlyreproduciblemethodofrescuinghearttissuefromundergoingirreversibleischaemicdamage.Majormilestonesregardingtheelucidationofthisphenomenonhavebeenpassedinthelasttwodecades.Volatileanaestheticsandopioidseffectivelyelicitpharmacologicalpreconditioning.Anaesthetic-inducedpreconditioningandischaemicpreconditioning(IPC)sharemanyfundamentalsteps,includingactivationofG-protein-coupledreceptors,multipleproteinkinasesandATP-sensitivepotassiumchannels(KATPchannels).Opioidsactivateδandκopioidreceptors,andthisleadstoproteinkinaseC(PKC)activation.ActivatedPKCactsasanamplifierofthepreconditioningstimulusandstabilizes,byphosphorylation,theopenstateofthemitochondrialKATPchannel(themainend-effectorinanaestheticpreconditioning)andthesarcolemmalKATPchannel.TheopeningofKATPchannelsultimatelyelicitscytoprotectionbydecreasingcytosolicandmitochondrialCa2+overload.
Thereiscompellingevidencethatpreconditioningoccursinhumans.However,thereareconflictingreportsontheefficacyofpreconditioninginthediseasedandagedmyocardium.Inaddition,manyanaestheticsandasignificantnumberofperioperativelyadministereddrugsaffecttheactivityofcardiacsarcolemmalandmitochondrialKATPchannels,theend-effectorsofcardiacpreconditioning,andtherebymarkedlymodulatepreconditioningeffectsinmyocardialtissue.AlthoughthesemodulatoryeffectsonKATPchannelshavebeeninvestigatedalmostexclusivelyinlaboratoryinvestigations,theymayhavepotentialimplicationsinclinicalmedicine.Importantquestionsregardingtheclinicalutilityandapplicabilityofperioperativecardiacpreconditioningremainunresolvedandneedmoreexperimentalworkandrandomizedcontrolledclinicaltrials.
Remifent
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