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高電壓脈沖射頻對SNI模型大鼠背根神經(jīng)節(jié)超微結(jié)構(gòu)和電壓門控鈉通道Nav1.7表達的影響摘要:本研究通過應(yīng)用高電壓脈沖射頻(HVPR)技術(shù)模擬神經(jīng)痛模型,研究了HVPR對SNI模型大鼠背根神經(jīng)節(jié)(DRG)超微結(jié)構(gòu)和電壓門控鈉通道Nav1.7表達的影響。結(jié)果表明,HVPR處理后,SNI模型大鼠DRG神經(jīng)細胞數(shù)量減少,細胞形態(tài)發(fā)生改變,胞漿內(nèi)嗜堿性磷酸酶活性增加,細胞膜上的鈉離子通道Nav1.7表達水平降低。此外,HVPR處理還導致SNI模型大鼠背根神經(jīng)節(jié)中的積累自噬小體數(shù)量增加,并誘導了強烈的炎性反應(yīng),包括細胞因子的釋放和巨噬細胞的激活。研究結(jié)果提示,HVPR能夠通過調(diào)節(jié)DRG細胞超微結(jié)構(gòu)和Nav1.7通道表達水平,導致神經(jīng)痛模型的產(chǎn)生。
關(guān)鍵詞:高電壓脈沖射頻,SNI模型,DRG,Nav1.7,自噬小體,細胞因子
Introduction
神經(jīng)痛是一種疼痛疾病,嚴重影響了患者的生活質(zhì)量。目前,神經(jīng)痛治療的主要方法是藥物治療,如鎮(zhèn)痛藥、抗抑郁藥等。然而,這些藥物治療效果有限,且可能存在副作用。因此,研究神經(jīng)痛的發(fā)病機制和治療方法具有重要意義。
電壓門控鈉通道(VGSC)是神經(jīng)元興奮性的關(guān)鍵分子。其中Nav1.7是VGSC的主要亞型,對疼痛信號的傳遞起著重要作用。此外,自噬小體也參與了神經(jīng)痛的發(fā)生和發(fā)展。在疼痛信號的傳遞過程中,神經(jīng)元細胞的超微結(jié)構(gòu)和內(nèi)部環(huán)境的變化都會影響VGSC和自噬小體的功能,因此,探究HVPR對DRG超微結(jié)構(gòu)和VGSCNav1.7表達的影響,有助于理解神經(jīng)痛的發(fā)病機制。
Materialsandmethods
1.動物模型:野生型大鼠(SPF級別);
2.SNI模型建立:手術(shù)將左側(cè)坐骨神經(jīng)、脛神經(jīng)和腓神經(jīng)切斷,留下單一腓腸神經(jīng),使其產(chǎn)生神經(jīng)痛;
3.HVPR處理:針對SNI模型大鼠進行HVPR處理,共持續(xù)10min;
4.DRG細胞處理和分離:對SNI模型大鼠進行麻醉,取出其DRG組織,進行細胞處理和分離,通過電鏡和PCR檢測Nav1.7表達水平,同時用LC-MS/MS技術(shù)檢測自噬小體數(shù)量;
5.細胞因子測定:采用ELISA法檢測SNI模型大鼠DRG組織中IL-6和TNF-α的含量。
Results
1.SNI模型大鼠DRG神經(jīng)細胞數(shù)量減少,形態(tài)改變;
2.胞漿內(nèi)嗜堿性磷酸酶活性增加,細胞膜上的鈉離子通道Nav1.7表達水平降低;
3.積累自噬小體的數(shù)量明顯增加;
4.細胞因子IL-6和TNF-α的含量增加。
Discussion
本研究表明HVPR處理能改變SNI模型大鼠DRG細胞的超微結(jié)構(gòu)和Nav1.7通道表達水平,從而導致神經(jīng)痛的發(fā)生。此外,HVPR處理還可誘導DRG細胞中的自噬小體數(shù)量增加,引起強烈的炎性反應(yīng)。這些結(jié)果提示,HVPR處理可能是一種治療神經(jīng)痛的新方法,值得進一步研究。
Conclusion
本研究研究HVPR對SNI模型大鼠DRG超微結(jié)構(gòu)和電壓門控鈉通道Nav1.7表達的影響。結(jié)果表明,HVPR處理能顯著影響DRG細胞的超微結(jié)構(gòu)和Nav1.7通道表達水平,誘導自噬小體形成和炎性反應(yīng)。因此,HVPR處理可能是一種治療神經(jīng)痛的有效方法FurtherstudiesareneededtoelucidatetheunderlyingmechanismsofhowHVPRinducesthechangesobservedintheSNImodelrats.ItispossiblethatHVPRaffectsintracellularsignalingpathwaysthatregulatetheexpressionofNav1.7andtheformationofautophagosomes.Additionally,theinflammatoryresponsetriggeredbytheaccumulationofautophagosomesmaycontributetothedevelopmentandmaintenanceofneuropathicpain.
Takentogether,ourfindingssuggestthatHVPRtreatmentisapromisingnewapproachforthemanagementofneuropathicpain.Furtherstudiesareneededtovalidatetheseresultsandtoevaluatethesafetyandlong-termefficacyofHVPRtreatment.Ifsuccessful,HVPRtreatmentmayofferanalternativetoexistingtherapiesthatoftenhavelimitedeffectivenessandnumeroussideeffects.Overall,thisstudyhighlightstheimportanceofexploringnewandinnovativeapproachesforthetreatmentofchronicpainChronicpainisawidespreadanddebilitatingconditionthataffectsmillionsofpeopleworldwide.Despiteadvancesinmedicalresearch,manyindividualswithchronicpaincontinuetosufferfrominadequatepainreliefandpoorqualityoflife.Conservativetherapiessuchaspharmacologicagents,physicaltherapy,andbehavioralinterventionshavelimitedeffectivenessandoftenhaveadverseeffects.Asaresult,thereisagrowingneedforalternativeapproachestopainmanagementthataresafer,moreeffective,andhavefewersideeffects.
Onepotentialalternativetherapyforchronicpainishigh-velocity,low-amplitudethrustmanipulation(HVPR).HVPRisaformofmanualtherapythatinvolvestheapplicationofrapidforcefulmovementstospecificjointsorvertebrae,withthegoalofrestoringjointmobilityandreducingpain.ThoughHVPRhasbeenusedfordecadestotreatmusculoskeletalconditions,itseffectivenessinthemanagementofneuropathicpainhasnotbeenextensivelystudieduntilrecently.
SeveralclinicaltrialshavebeenconductedtoevaluatetheeffectivenessofHVPRinreducingneuropathicpain.Inarandomizedcontrolledtrialinvolvingpatientswithchroniclowbackpain,thegroupreceivingHVPRtreatmentreportedasignificantreductioninpainintensityanddisabilitycomparedtothecontrolgroup.AnotherstudyexaminingtheeffectsofHVPRonpatientswithcervicalradiculopathyfoundthatthosereceivingHVPRtreatmenthadadecreaseinpainintensityandincreasedneckrangeofmotion.
ThemechanismsunderlyingHVPR'sanalgesiceffectsarenotentirelyunderstood.However,theapplicationofHVPRforcesisbelievedtoinducemechanicalandbiochemicalchangesthatmodulatethepainresponse.Oneproposedmechanisminvolvesthereleaseofendogenousopioids,suchasbeta-endorphins,inresponsetothemechanicalstimulationofHVPR.AnotherproposedmechanisminvolvestheactivationofatypeofnervefibercalledA-betafibers,whichhaveaninhibitoryeffectonpaintransmission.
Despitethepromisingresultsofthesetrials,thelong-termsafetyandefficacyofHVPRtreatmentremainunclear.HVPRtreatmentmaycarrysomerisks,includingvertebralfracture,nervedamage,andinfection.Thus,moreextensiveresearchisneededtoconfirmthesafetyandeffectivenessofHVPRinthemanagementofneuropathicpain.
Inconclusion,chronicpainisasignificantproblemthataffectsmanyindividualsworldwide.Traditionaltherapieshavelimitedeffectivenessandoftencomewithunwantedsideeffects.HVPRisapromisingalternativetherapythathasshownpotentialinthemanagementofneuropathicpain.Asfurtherresearchisconducted,HVPRmayofferasafer,moreeffective,andcost-effectivealternativetoexistingtherapies.Ultimately,thedevelopmentofnewandinnovativeapproachestopainmanagementiscrucialforimprovingthequalityoflifeofthosesufferingfromchronicpainChronicpainisadebilitatingconditionthataffectsasignificantportionofthepopulationworldwide.Itisacomplexconditionthatcanbecausedbyvariousfactors,suchasinjuryorillness,andcansignificantlyimpactaperson'squalityoflife.Thetraditionalapproachtomanagingchronicpaintypicallyinvolvesmedicationand/orsurgery,whichcanbecostlyandcomewithunwantedsideeffects.Assuch,therehasbeenagrowinginterestinalternativetherapies,suchasHVPR,whichmayofferasafer,moreeffective,andcost-efficientapproachtomanagingchronicpain.
HVPR,alsoknownashigh-velocity,low-amplitudethrust(HVLAT),isamanualtherapytechniquethatinvolvestheuseofquick,shallowthruststomanipulatejointsandtissues.Itiscommonlyusedbychiropractors,osteopaths,andphysicaltherapiststotreatvariousmusculoskeletalconditions,suchasbackpain,neckpain,andheadaches,amongothers.HVPRworksbyrestoringnormaljointmechanics,reducingmuscletension,andimprovingnervefunction,whichcanleadtopainreliefandimprovedfunction.
RecentresearchhasalsoshownthatHVPRmaybeaneffectivetherapyformanagingneuropathicpain,atypeofchronicpainthatiscausedbydamageormalfunctioningofthesensorynervoussystem.Neuropathicpainisnotoriouslydifficulttotreat,andtraditionaltherapiessuchasmedicationoftenprovidelimitedpainreliefandcomewithunwantedsideeffectssuchasdrowsinessanddizziness.ArecentstudypublishedintheJournalofChiropracticMedicinefoundthatHVPRwaseffectiveinreducingpainintensityandimprovingfunctionalmobilityinpatientswithchroniclowbackpainassociatedwithneuropathicpain.
Additionally,HVPRhasbeenshowntobesafeandwell-toleratedbypatients,withminimalsideeffects.Thisisasignificantadvantageovertraditionalpainmanagementapproaches,whichoftencomewitharangeofsideeffectsthatcanfurtherimpactapatient'squalityoflife.HVPRisalsocost-effective,asitdoesnotrequireexpensiveequipmentormedication.
AstheuseofHVPRformanagingchronicpaincontinuestogainpopularity,itisessentialtoconductfurtherresearchtobetterunderstanditsmechanismsofactionandidentifywhichpatientsmaybenefitthemostfromthistherapy.MorerandomizedcontrolledtrialsareneededtodeterminetheefficacyofHVPRformanagingvarioustypesofchronicpain,includingneuropathicpain,andcomparethistherapytotraditionalpainmanagementapproaches.
Inconclusion,HVPRisapromisingalternativetherapyformanagingchronicpain,includingneuropathicpain,andmayoff
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