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LiLin(李林)DepartmentofPharmacologyXuanwuHospital03/11/2016Tel:83198886;ClinicalPharmacologyIntroduction2Whatisclinicalpharmacology?Whydoweneedtostudyclinicalpharmacology?ContentsofclinicalpharmacologyPharmacogenomics
PrinciplesofrationaldruguseToday’stopics1930’s,theconcept
ofClinicalPharmacologywasfirstproposed1954,
thefirstdivision
ofClinicalPharmacology
wasestablishedatJohnHopkinsUniversity,USA1960s,
thalidomidedisastershockedtheworld;inducedmuchattentiontoClinicalPharmacology1980,thefirstinternationalcongressofClinicalPharmacologywasheldinLondonevery4years,
IUPHARhostsWorldCongressofBasicandClinicalPharmacologyHistoryofClinicalPharmacology1980,
thefirstInstituteofClinicalPharmacologyinChinawasestablishedinBeijingMedicalCollege1982,ClinicalPharmacologyBranchofChinesePharmacologySocietywasfounded1983,ClinicalPharmacologyBases
wereapprovedbyMinistryofHealthofChina,fornewdrugevaluation
InChina
I.Whatisclinicalpharmacology?Pharmacology:
Thestudyofthe
interactionofchemicalswithlivingsystems
ClinicalPharmacology:
Thestudyofthe
interactionofdrugswithhumanbody.Object:humanbodyBasis:
pharmacology,clinicalmedicineWhatisclinicalpharmacokinetics?Pharmacokinetics(PK,藥物代謝動(dòng)力學(xué)):
theactionsof
thebodyonthedrug
Clinicalpharmacokinetics
(臨床藥代學(xué)):theactionsof
humanbody
onthedrug
Including:absorptiondistribution
metabolismexcretionWhatisclinicalpharmacodynamics?
Pharmacodynamics(PD,藥物效應(yīng)動(dòng)力學(xué)):
theactionsofadrug
onthebody.Clinicalpharmacodynamics
(臨床藥效學(xué)):theactionsofadrug
onhumanbody.
Including:receptorinteractions,dose-responsephenomena,mechanismsoftherapeuticandtoxicaction8DrugHumanBody?absorption,distributionmetabolism,excretion?DrugeffectsanditsmechanismIncludingreceptorinteractionsdose-responsephenomenamechanismsoftherapeuticandtoxicactionII.Whydoweneedtostudyclinicalpharmacology?
1.GuaranteethesafeuseofclinicaldrugsDrug-inducedsevereharmevent:
1960s,Germany:Thalidomide:(沙立度胺,“反應(yīng)?!?stoppregnancysick
but………
11
Thalidomidedisaster12,000seal(海豹)children,
>6000diedNow:thalidomide
(沙立度胺)Indication:(適應(yīng)證)
erythemanodosumleprosy
(麻風(fēng)結(jié)節(jié)性紅斑)1998,FDAofUSA
multiplemyeloma
(多發(fā)性骨髓瘤)
2006,FDAofUSACaution:
(警告)1.GuaranteethesafeuseofclinicaldrugsThisdrughasstrongteratogenic(致畸)
action,
andisabsolutelyforbiddeninpregnantwomen.Thekeyistounderstandthecharacteristicsofdrugs
inhumanbodyespeciallywhentreat
complicatedpatients
critical(危重)patients,inICUmultipleorganfailure(多臟器衰竭)patientsII.Whydoweneedclinicalpharmacology?2.ElevatetheleveloftherapyManydiseaseslackeffectivetreatment(cancer,Alzheimer’sdisease,……)Newdrugresearchanddevelopment(R&D)Clinicalevaluationofnewdrugsismostimportant
II.Whydoweneedclinicalpharmacology?3.DevelopnewdrugsIII.Maincontentsofclinical
PharmacologyFourbasicprocessesofdrugtherapy1.Selectionofdosageform:
drugentershumanbodydosageform(劑型)oral
injectgastro-intestinallivermetabolismextracellularwater
proteinbinding
non-binding
actionsite2.Pharmacokineticprocess:
drugarrivesactionsiteelimination(kidney,liver)
first-passeffectpharmacologicalactiontherapeuticeffect(治療作用)3.Paharmacodynamicprocess:
drugproducespharmacologicalactiononhumanbody4.Therapeuticprocess:
pharmacologicalactionturnsintotherapeuticeffect
actionsitedesiredundesiredadversedrugreaction(ADR)(藥物不良反應(yīng))(Aspirininhibitsplateletaggregation)
阿司匹林抑制血小板聚集(preventsthrombosis)
防止血栓形成(inducescerebralhemorrhage)
引起腦出血(Aspirintreatsischemiccerebrovasculardisease)治療缺血性腦血管病1.Clinicalpharmacokinetics
(臨床藥代學(xué))(1)Contentofstudy:
Thetransport(轉(zhuǎn)運(yùn))
andtransform(轉(zhuǎn)化)
processesofdrugsinhumanbody,
including:
absorption,distribution,metabolism,excretion
(2)MainmethodMonitorthebloodconcentration
ofdrug
(血藥濃度監(jiān)測(cè))
III.MaincontentsofclinicalpharmacologyBloodconcentration--timecurveaftersingledrugdoseHalf-life(T1/2)半衰期(MEC:minimumeffectiveconcentration)峰濃度達(dá)峰時(shí)間最低有效濃度20(3)Themostimportantparametersbioavailability(生物利用度):
thefractionofdrugabsorbedintothesystemiccirculation.volumeofdistribution(分布容積):
theapparentspace(表觀空間)inthebodyavailabletocontainthedrugeliminationhalf-life(消除半衰期):therateofremovalofdrugfromthebodyclearance(清除率):
thebody’sefficiencyineliminatingdrug21(4)SignificanceofstudyProvideevidenceformakingtheplan
ofdrugadministration
(制定給藥方案)(dose,interval)Dosingrate=CL?Css(清除率?穩(wěn)態(tài)血濃度)
(CL:clearancefromthesystemiccirculation,Css:
thesteady-stateconcentrationofdruginblood)
CL=Vm/(Km+C)
(C:
concentrationofdruginblood)
1.Clinicalpharmacokinetics2.Clinicalpharmacodynamics
(臨床藥效學(xué))(1)ContentsofstudyFunctionchanges
ofhumanbodyinducedbydrugactionActionandmechanismofdrug
(receptorinteractions,etc.)RelationshipbetweendoseandeffectofdrugIII.Maincontentofclinicalpharmacology(MEC:minimumeffectiveconcentration)最低有效濃度Therapeuticgoal:
obtainandmaintainconcentrationswithinthetherapeuticwindowforthedesiredresponsewithaminimumoftoxicity.
Drugresponse
belowMECforthedesiredeffect:
subtherapeutic(未達(dá)治療劑量的),
aboveMECforanadverseeffect:toxicity
Therapeuticwindow(治療窗)3.Adversedrugreaction(ADR)藥物不良反應(yīng)(1)Contentsofstudysideeffect 副作用toxiceffect 毒性反應(yīng)anaphylacticreaction 過(guò)敏反應(yīng)dependence 依賴(lài)性withdrawsyndrome撤藥綜合征carcinogeniceffect致癌作用teratogeniceffect致畸形作用
III.MaincontentofclinicalpharmacologyForexample:
Antibioticsabuse(抗生素濫用)
floraimbalance菌群失調(diào)
secondaryinfection繼發(fā)性感染
drugresistance耐藥性(2)Physician-induceddiseasesHormoneabuse(steroid類(lèi)固醇)hepatonecrosis肝壞死
osteonecrosis骨壞死
liver
(drugsthat
maydamageliver,patientswithliverdisease)
kidney(drugsthatmay
damagekidney,
patientswithkidneydisease)
pregnantwomen:
teratogenicaction(致畸作用)
oldpeople:theclearanceofmanydrugsisdecreased
Whatshouldwedo?
(3)PaymuchattentionOrgans
Specialpopulation(特殊人群)01/27/2014,
ADRInformationNotification(59th):
“Bevigilantto(警惕)severeADRofCefazolin
(頭孢唑林)
injection”
2013,theCenterreceivedADRreportsof349cases,mainly:systemicdamage(shock89cases),respiratorydamage,skindamage
NationalCenterforADRMonitering,China
國(guó)家藥品不良反應(yīng)監(jiān)測(cè)中心29Doctor’sresponsibilityAdoctorwhodoesonlyasimplething
mayrescuemanypeople’slifeandhealth.
Todiscoverandreportadversedrugreaction(ADR).
--Chiefeditor,JournalofADR
4.Interactionofdrugs
藥物相互作用
Contentsofstudy:Changesineffectsoftwoandmoredrugswhentheyareusedsimultaneously
(同時(shí))oroneafteranother.
III.MaincontentofclinicalpharmacologyHepaticdrug-metabolizingenzyme(肝藥酶)About
50CYParefunctionallyactiveinhumanTheyarecategorizedinto
17families8to10isoformsinthe
CYP1,CYP2,CYP3
areinvolvedinthemajorityofalldrugmetabolismreactions
inhumanbeings.CytochromeP-450(CYP)細(xì)胞色素P-45032CYP3A4andCYP3A5areinvolvedinthemetabolismofabout50%ofdrugs.IsoformsintheCYP2CfamilyandCYP2D6subfamilyalsoareinvolvedtoalargeextentinthemetabolismofdrugs.
Awomantakescarbamazepine
(卡馬西平)
totreatepilepsy(癲癇).Complain:unplannedpregnancy.Why?
Co-administrationofantiseizure
(抗癲癇藥)
andoralcontraceptives
(口服避孕藥)CarbamazepineinducesCYP3A4.OralcontraceptivesaremetabolizedbyCYP3A4.Whathappens?Treatmentwithcarbamazepinecanenhancethedegradationoforalcontraceptives.5.Clinicalresearchandevaluation
ofnewdrugs
III.MaincontentsofclinicalpharmacologyEverynewdrugmustcompleteclinicaltrials
before
itsmanufactureisapprovedClinicalpharmacologyresearchplaysthemostimportantroleinnewdrugdevelopment
IV.Pharmacogenomics
藥物基因組學(xué)
36Newwords:
gene(基因)
genome
(基因組)
genomics(基因組學(xué))
pharmacogenomics(藥物基因組學(xué))Whatispharmacogenomics?studyofthegeneticvariations(遺傳變異)
thatcauseindividualdifferencesindrugresponse37
*
Enzymesthathavefunctional
allelicvariants(等位基因變異)38CPY2D6hasgeneticpolymorphisms
(基因多態(tài)性)inCYP2D6gene:about
70singlenucleotidepolymorphisms(SNP,單核苷多態(tài)性)Asaresult,4phenotypicsubpopulations(顯型亞群)ofmetabolizers
(代謝者)exist:poor(PM),intermediate(IM),
extensive(EM),ultra-rapid(UM)39CPY2D6Morethan65
commonlyuseddrugsaremetabolizedbyCYP2D6,tricyclicantidepressants(三環(huán)類(lèi)抗抑郁藥)opiates(阿片制劑)TheclinicalimportanceoftheCYP2D6polymorphism:PMs:ADRorinefficacy?Ums:ADRorinefficacy?40SignificancePrecisionmedicine(精準(zhǔn)醫(yī)學(xué))2015,USAPresident
Obamaproposed“Precisionmedicineplan”:basedongenomic(基因組學(xué))andproteomic
(蛋白組學(xué))
detection,
t
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