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1、针刺镇痛相关受体及正电子配基研究进展作者:王慧春,左传涛,管一晖【关键词】针刺镇痛;电针;受体;正电子发射断层扫描;放射性配基Asatraditionaltreatmentmethod,acupuncturecanbeelioratepathologicprocesses,andthecapitalapplicationisanalgesia.Manystudies,includingneurobiochemisitry,histopathologyandradioligandbindingassayofreceptor,
2、shoediatedbyvariousneurotransmitters,neuropeptides,modulatorsandreceptors[13].Hoitedastheyalexperiments.Accordingtocharacteristicsofreceptorligandbindingdomains,positronemissiontomography(PET)receptorimaginghaditssuperiorityinrealtimelyinvestigatingthedistribut
3、ion(localization),quantity(density)andfunction(affinity)ofthetracereceptorsinvivoechanismofAAandpromotereasonableapplicationofacupunctureifthePETreceptorimagingshouldbeusedinAAresearch.Asagingtoselectthesuitableradioligand,therefore,thepresentarticlerevieentmethod
4、ofstimulationproducinganalgesia,acupuncturecanrelievepainbyactivatingthepainrelatedreceptorsinbrain,ajorneurochemicalsubstancesinvolvedinAA[1,2].Opiatereceptors(ORs)arealanbrain,andthenformedtheconceptofthreegroupsofORs(μ,κ,δ).From1970s,manyEOPsorethanthirtyyears
5、,andfourclassesofORligandshavebeendeveloped,includingμ,κ,δ,OFQRandendomorphin(EM),DYN,ENK,orphaninFQ(OFQ)andtheirrespectiveprecursors[4].ThepreviousstudiesofAAmechanismsfoundthatnaloxone,aμreceptorantagonist,couldpartiallyreversetheanalgesiceffectsofacupuncturein
6、mice[2].ThelevelofβEPinhumancerebrospinalfluidinistrationofvariousspecificantagonistsorantiseraofORsubtypes,Han[5]uncoveredthat2and100HzEAinducedanalgesiaeffectsediatedbyμ/δandκreceptorsintheratspinalcordrespectivelyunderthephysiologicalpainconditions.Threeclasse
7、sofEOPs(μ、κandδ)couldbereleasedsimultaneouslybyusingloent[6]associatedmatorypaininratsinistrationofμandδreceptorantagonists.HoanifestedthatEAinducedtheanalgesiceffectsviaactivatingμandδreceptorsbutnoκreceptorunderthepathologicconditions,ainsmediatinghighandloalsp
8、ecies,typesofpain,routesanddosesofadministrationorsitesofactioninedbystimulatingthedifferentOFQRsubtypes[7].1.2ORPETradioligands11Cdiprenorphine(DPN)an