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Chapter8
LocalAnaesthetics
SARandclassificationActionandmechanismApplicationModesADRCommonanaestheticsLocalanaesthetics
--reversiblyblockimpulseconductionalongnerveaxonsandotherexcitablemembranes,canbeclinicallyusedtoblockpainsensation.--Patientsareconscious,showanalgesisoflocaltissueinordertodolocaloperation.Cocaine
--thefirstagent,wasisolatedfromcocaleavesin1860.Part1.StructureandclassificationElementarystructure
lipophilicgroup:aromaticringorheterocycle
hydrophilicaminesubstituents
intermediatechainClassification
esterbond:aromaticesters
procaine
amidelinkage:amides
lidocaineLocalanestheticincludesestersandamidesprocainetetracainelidocainebupivacaine
Structure-ActivityRelationship
Lipidsolubility:duetoaromaticring,facilitatetocrosscellmembranetoexertlocalanaesthesia.esterswithhighlipidsolubilityusuallyhaveashorterdurationofaction.
Hydrophilicalkylamine:Localanestheticsareweakbases.Fortherapeuticapplication,theyareusuallymadeavailableassaltsforsolubilityandstability.Structure-ActivityRelationship
Esters:hydrolysisbylipaseinplasma.
Amides:degradationbyamidaseinliver.comparedtwotypes,amideshasquickonset,broaddiffusion,longerdurationandstablization.Part2.Actionandmechanism
[PharmacologicalActions]1.Localanaesthesia↑excitingthreshold,↓actionpotential,↓conductionrate
Theactiondegreeisrelatedthefiberstype.Smallerfibersareblockedfirst.Terminal,ganglion,synapsishavehighsensitivity.Nervefiberswithoutmyelinsheatharemoresensitivethanthosewithmyelinsheath.Anaesthesiainorderofpainfibers>othersensations>motorfunction痛覺>溫覺>觸、壓覺>中樞抑制性神經(jīng)元>中樞興奮性神經(jīng)元>自主神經(jīng)>運(yùn)動(dòng)神經(jīng)>心肌>血管平滑?。疚改c平滑?。咀訉m平滑?。竟趋兰PharmacologicalActions]2.Anti-arrhythmiaLidocaine:commonusedinventriculartachycardia,suchasVT,VF,etc.3.GeneralreactionExertadversereactionbyabsorption.cellmembranestabilizingaction
(膜穩(wěn)定作用)---blockadeofvoltage-gatedsodiumchannels
(鈉通道阻滯作用)
→inhibittogenerateanactionpotential→blockadeoftheproduceandconductionofnerveimpulse[MechanismofAction]1)Twomolecularstatesofanaesthetics:
--un-ionizedform(B)--cationicform(ionizedform,BH+)TherelativeproportionsoftwoformsisregulatedbytheirpKaandthe
pHofbodyfluids.Bformcouldpenetrateintocells,thenchangedtoBH+form.Thecationicform(BH+)bindstophosphategroup(negativecharge)ofNa+channeltoblocktheopenofchannel→↓Na+influx.
Reason:sincethepKaofmostlocalanestheticsisintherangeof8.0-9.0,intracellularpHis7.08.2)Lipidsolubility,dissociationrateanddegreeofdrugsarerelatedtotime-activityoflocalanaesthesia.Thecationicformisthoughttobethemostactiveformatthereceptorsite,buttheunionizedformisveryimportantforrapidpenetrationofbiologicmembranes.MechanismofactionBlockingvoltage-gatedsodiumchannelsbycationicforminsidethecellPart3.Modesoflocalanesthesia
1.surfaceanaesthesia(ortopical
anaesthesia,表面麻醉)2.infiltrationanaesthesia(浸潤(rùn)麻醉)3.conductionanaesthesia(傳導(dǎo)麻醉)
---blockanaesthesia
(阻滯麻醉)4.subarachnoidalanaesthesia(蛛網(wǎng)膜下腔麻醉)---spinalanaesthesiaorlumbaranaesthesia5.epiduralanaesthesia(硬脊膜外麻醉)
---將穿透力強(qiáng)的局麻藥噴或涂于粘膜表面,使粘膜下神經(jīng)末梢麻醉。---適用于口腔、鼻、咽喉、眼睛、尿道等粘膜部位的淺表手術(shù)。
tetracaine
surfaceanaesthesia(表面麻醉)---將局麻藥注入手術(shù)野皮下或手術(shù)區(qū)各層組織里,使局部的神經(jīng)末梢麻醉。---常用于淺表小手術(shù)。lidocaine,procaine
infiltrationanaesthesia(浸潤(rùn)麻醉)
----是將局麻藥注射到神經(jīng)干附近,阻止神經(jīng)沖動(dòng)傳導(dǎo),使其支配的區(qū)域產(chǎn)生麻醉。----常用于四肢及口腔手術(shù)。lidocaine,bupivacaine,ropivacaineconductionanaesthesia(傳導(dǎo)麻醉,阻滯麻醉)---也叫脊麻、腰麻。將局麻藥液經(jīng)腰椎間隙注入蛛網(wǎng)膜下腔,以阻滯該部位的神經(jīng)根,使神經(jīng)根所支配的部位產(chǎn)生麻醉,麻醉范圍較廣。---適用于下腹部及下肢的手術(shù)。
bupivacaine,lidocaine,procaine
subarachnoidanaesthesia(蛛網(wǎng)膜下腔麻醉)
---將局麻藥液注入硬脊膜外腔,使通過此腔穿出椎間孔的神經(jīng)根麻醉。---可用于頸部到下肢的手術(shù),尤其適用于上腹部手術(shù)。
lidocaine,bupivacaine,ropivacaine
epiduralanaesthesia(硬脊膜外麻醉)Section4.AbsorptionandAdverseReaction
Localanestheticagentsareabsorbedfromthesiteofadministration----absorptiveaction:A.CentralNervousSystemB.CardiovascularSystemC.HypersensitiveReactionsD.AllergicReactionsA.CentralNervousSystem:
Atlowdoses,sedation,headache,dizziness,hypesthesia,cloudingofconsciousness.(inhibition)Athigherdoses,insanity,andmusculartwitching,evenconvulsion.(excitation)Finally,inhibitionofbothinhibitiveandexcitedneurons→overallinhibitionofCNS→coma,cardiacarrest,respiratoryparalysis,andevendeath.B.CardiovascularSystem:
Na+channelblockade→heartinhibition→myocardialcontractility↓,conduction↓,prolongERP;Vasodilation
→BP↓,evenshockGenerally,CNStoxicitypriortoCVStoxicity;
Bupivacaine(conversely),severeCVStoxicity,includingarrhythmiaandlethalVF.
C.HypersusceptibilityReaction:
Somepatientstreatmentwith<1/3highdose,showtoxiceffects,suchasfaint,respiratorydepression,circulatoryfailure.Duetoindividualdifference.Note:Foroneperson,thesensitivitytodrugsmaychangedobviouslyatdifferentphysiologicalorpathologicalstatus.D.AllergicReactions(Anaphylaxis):
Theestertypelocalanaestheticsaremetabolizedtop-aminobenzoicacid(PABA)derivatives.Thesemetabolitesareresponsibleforallergicreactionsinasmallpercentageofthepopulation.Symptom:Urticaria(蕁麻疹),bronchospasm,dyspnea,hypotensionandangioedema.Esters>amidesSection5.CommonLocalanaesthetics1.Procaine(普魯卡因)instabilityofaqueoussolution,lesstoxicityinfiltrationanaesthesia;conductionanaesthesiasubarachnoidalandepiduralanaesthesia(needauxiliarysolvent)badpenetratingpower,
notusedinsurfaceanaesthesia
2.Lidocaine
(利多卡因)
strongpenetratingability
quickandstrongaction
surfaceanaesthesia,
infiltrationanaesthesia,
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