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ANALGESICSsss
ThewordanalgesicderivesfromGreek
an(without)andalgos(pain).
Drugsthatselectivelyinhibittheperception(sensation)ofpain
.
Analgesic any drug that relieves pain selectively
withoutblockingtheconductionofnerveimpulses,markedly
alteringsensoryperception,or affectingconsciousness.
Thisselectivityisanimportantdistinctionbetweenananal
gesicandan anesthetic.
CLASSIFICATIONOF
ANALGESICS
Analgesicaredividedintotwomain groups.
ANALGESICS
Opioidan
algesics
Nonopioida
nalgesics
Naturalopium
alkaloids
Semi-
synthetic
opiates
synthetic
opioids
OPIOIDANALGESICS
Narcotics/morphinelikeanalgesicsareincludedinthiscate
gory.Theopioidanalgesicswereonce
callednarcoticdrugsbecausetheyactonthebrainandcaninduc
e sleep. The opioid analgesics can be used for eithershort-
termorlong-termreliefofseverepain.
SUBCLASSESOFOPIOID
Furtherdividedintothreesubclasseswhichare;
 Naturalopium alkaloids
• Morphine
• Codeine(mostcommonlyusestronganalgesic,less addictivethan
morphine,similartomorphineexceptforthereplacementofaOHgroup
with OCH3group).
Methadone
• Hydromorphone
•

CONTINUE…
 Semi-synthetic opiates
 Diacetylmorphine
 Oxymorphone
 Pholcodeine
 Synthetic opioids
Pethidine
 Methadone
 Dextropropoxyphene
NONOPIOIDANALGESICS
NSAIDS (non-steroidal anti-inflammatory drugs) /
nonnarcotics/aspirinlikeanalgesics
 Nonopioidanalgesicswhichalleviatepainbyreducinglocal
inflammatory responses. In contrast, the anti-inflammatory
compounds are used for short-term pain
reliefandformodestpain,suchasthatofheadache,musclestrain,
bruising,orarthritis.
PAIN
Aprotectivemechanismtowarnofdamageorthepresenceofdisea
se.
PAIN
ACUTE
PAIN
CHRONIC
PAIN
CLASSIFICATIONOFPAIN;
On basisof onsetanddurationtherearetwotypesof pain
ACUTEPAIN
Suddeninonset.
Usuallysubsidesoncetreated.
CHRONICPAIN
Persistent (continual) or recurring (happen or occur again).Often
difficult totreat.
MAJORSOURECSOFPAIN
Source Areainvolved Characteristics treatment
Somatic Body framework ThrobbingStabbin
g(sharp)
Narcotics
NSAIDs
visceral KidneysIn
testinesLi
ver
Aching
(usuallymoderat
elypain)Throbbi
ng
Narcotics
NSAIDs
neuropathic Nerves Burning
Tingling
Narcotics
NSAIDs
AntidepressantsA
nticonvulsants
Non opioid analgesics ( anti-
inflammatoryanalgesics)
Mostanti-
inflammatoryanalgesicsarederivedfromthreecompoundsd
iscoveredinthe19thcentury
 salicylicacid,
 pyrazolone,
 phenacetin(oracetophenetidin).
 Althoughchemicallyunrelated,thedrugsinthesefamilieshav
e the ability to relieve mild to moderate pain
throughactionsthatreduceinflammationatitssource.
SALICYLICACID
�SalicylicacidhastheformulaC7H6O3.
�itiscolorlesscrystallineorganicacid.
� Salicylic acid as a medication is used most commonly to help remove the
outerlayer of the skin. As such, it is used to treat warts (Warts are typically
small,rough, andhardgrowths thataresimilarincolortothe restof theskin)
psoriasis(Psoriasis is a long-lasting autoimmune disease characterized by
patches ofabnormalskin.Theseskinpatchesaretypicallyred,itchy,and
scaly),dandruff,acne,ringworm(Dermatophytosis,alsoknownasringworm, isa
fungalinfectionoftheskin).
3-PYRAZOLONE 5-PYRAZOLONE
PYRAZOLONE
The drugs of these families have the ability to relieve mild
tomoderatepainthroughactionsthatreduceinflammationatitsso
urce.
PHENACETIN
Phenacetin(oracetophenetidin)is apain-relievingand fever-reducingdrug,whichwas
widely used between its introduction in 1887 and the 1983 ban imposed
bytheU.S.Foodand DrugAdministration.
Mechanismofactions;
itsanalgesiceffects areduetoitsactionson thesensory tractsof
thespinalcord.Inaddition,phenacetinhasadepressantactionon theheart,whereitactsas
a
negativeinotrope.Itis an antipyretic,actingon thebraintodecreasethe temperatureset
point. It is also used to treat rheumatoid arthritis (Rheumatoid arthritis (RA) is
along-term autoimmune disorder that primarily affects joints. It typically results
inwarm, swollen,and painfuljoints).Itis metabolizedinthe body
toparacetamol(acetaminophen),whichis alsoaclinicallyrelevantanalgesic.
Ahand affectedbyrheumatoidarthritis
SALICYLICACID
DERIVATIVES;
Acetylsalicylicacid,or
aspirin,whichisderivedfromsalicylicacid,isthemostwid
elyusedmild analgesic.
Itisconsideredtheprototypefor anti-
inflammatoryanalgesics.
PHENACETINDERIVATIVES;
Acetaminophen (a derivative of phenacetin) and the aspirin-
likedrugs,ornonsteroidalanti-
inflammatorydrugs(NSAIDs),which include compounds such
as ibuprofen, naproxen, andfenoprofen.
PYRAZOLONEDERIVATIVES
�Pyrazolone derivatives, with some exceptions, are
nolongerwidelyusedinmanycountries,becauseoftheirte
ndencytocauseanacuteinfectionknown
as agranulocytosis (Agranulocytosis, also known
asagranulosis or granulopenia, is an acute
conditioninvolving a severe and dangerous leukopenia
(loweredwhite blood cell count), most commonly of
neutrophilscausing a neutropenia in the circulating
blood. It is aseverelackofonemajor classofinfection-
fightingwhitebloodcells).
MECHANISMOFACTIONS
�Inhibitionofthesynthesisofprostaglandins;
�Aspirin and NSAIDs appear to share a similar molecular
mechanismofaction—namely,inhibitionofthesynthesis
ofprostaglandins(naturalproductsofinflamedwhitebloodcells)thatinduc
e the responses in local tissue that include pain andinflammation.
� In fact, aspirin and all aspirin-like analgesics, including
indomethacinand sulindac, which are derived from a heterocyclic
organiccompound known as indole, inhibit prostaglandin synthesis
andrelease.
CONTINUE….
�Divisionofagents;
AlltheseagentscanbefurtherdividedintononselectiveCO
XinhibitorsandselectiveCOXinhibitors.
�COX,orcyclooxygenase;
COX,orcyclooxygenase,isanenzymeresponsibleforthesynt
hesisofprostaglandinsandrelatedcompounds.
CONTINUE…
�FormsofCOX;
Ithastwoforms.COX-1 andCOX-2
�COX-1,which isfoundinmostnormaltissues.
�COX-2, which is induced in the presence of
inflammation.BecauseCOX-
2isnotnormallyexpressedinthestomach.
CONTINUE…
�AdvantageofCOX-2inhibitors;
The use of COX-2 inhibitors (e.g., rofecoxib, celecoxib) seems
toresult in less gastric ulceration than occurs with other anti-
inflammatory analgesics, particularly aspirin. However, COX-
2inhibitorsdo notreducetheabilityofplateletsto
formclots,abenefitassociatedwithaspirinandothernonselectiveCOX
inhibitors.
COMPARISON
�PreferencesinCOXselectivityandthepossibilityofadditionalmolecularactio
nsofNSAIDsmayexplaindifferencesinthetherapeuticeffects between
aspirin, acetaminophen, and NSAIDs. For example,aspirin is effective
in reducing fever, as well as relieving inflammation,while
acetaminophen and NSAIDs are more potent antipyretic (fever-
reducing) analgesics. Acetaminophen,ontheotherhand, possessesinferior
anti-inflammatory activity compared with aspirin and NSAIDsand thus
is relatively ineffective in treating inflammatory
conditionssuchasrheumatoidarthritis.
CONTINUE…
�Despite this, acetaminophen is a popular mild analgesic
andantipyretic and is a suitable alternative to aspirin for patients
whodevelopseveresymptomsofstomachirritation,becauseitisnotash
armful tothe gastrointestinaltract.
COMMONLYUSED
ACETOMINOPHIN
�Paracetamol(N-acetyl-P-Aminophenol)
�Itisanalgesicandantipyreticdrug.
�Orallyinduceddrughasmaximaleffects oftwo tofourhours.
�Overdosescauses damagingof liverandkidneys.
SIDEEFFECTS
�As might be expected from their common mechanisms
ofaction, many of the anti-inflammatory analgesic
drugssharesimilarsideeffects.
HYPERSENSITIVITY
�Hypersensitivityresponsestoaspirin-likedrugsarethoughttobedue to an
accumulation of prostaglandins after the pathways
thatbreakdownprostaglandinsareblocked.Theseresponsescanbefatal
whenverystronganti-inflammatorycompounds aregiven.
PEPTIC ULCERS, LIVER DAMAGE
&RENALTOXICITY
�Inhibition of prostaglandin synthesis may result in other serious
sideeffects, such as peptic ulcers and a reduced ability of platelets
in thebloodto aggregateandformclots.
�Liver damage occasionally occurs after administration
ofacetaminophen.
�Renaltoxicityissometimesseenwith useofNSAIDs.
ASPIRINSIDEEFFECTS
Aspirinitself,takeninoverdose,cancause
�Deafness
�Ringingintheears
�Diarrhea
�Nausea
�Headache,whichdisappearwhenthedoseisreducedor stopped.
�Reyesyndrome
REYESYNDROME
�Aspirin is also thought to be a causative agent of Reye syndrome, a
rareandseriousdegenerativediseaseof
thebrainandfattytissueoftheliverthataccompaniescertainviralinfectionsin
childrenandyoungadults.
Someaspirin-likeanalgesicsalsohavespecifictoxiceffects
OPIOIDANALGESICS
�The term opioid has been adopted as a
generalclassification of all those agents that share
chemicalstructures, sites, and mechanisms of action
with
theendogenousopioidagonists(endogenoussubstancesare
thoseproducedinsidethehumanbody).
GROUPOFENDOGENEOUSSUBSTANC
ES
�There are three groups of endogenous substances
whichare;
�Enkephalins
�Stimulatesdeltareceptors
�Endorphins
CONTINUE…
�Actonmuanddeltareceptors
�Reducespainandhaspositiveeffectonbrain
�Dynorphins
�Stimulatesthekappareceptors
�Allthreehaveopioidlikeactionsandarefoundinthebody
� They are naturally occurring peptides that possess analgesic action and
addictionpotential.
�Thesereceptorscanbeblockedby naloxone,whichisa morphineantagonist.
OPIOIDSUBSTANCES
�Opioidsubstancesencompassallthenatural
and synthetic chemical compounds closely
relatedto morphine, whether they act as agonists
(cellularactivators)orantagonists(substancesthatblo
cktheactionsofagonists).
ADDICTIVEDRUGS
�Although interest in these drugs had always been
highbecause of their value in pain relief and because
ofproblemsofabuseandaddiction,interestintensifiedinthe19
70s and ’80s by discoveries about the naturallyoccurring
morphine like substances, the
endogenousopioidneuropeptides.
OPIUM
�Opiumis thepowder from thedried
juiceofthepoppyPapaversomniferum.
�When taken orally, opium produces sleep and induces a state
ofpeacefulwell-being.
�ItsusedatesbackatleasttoBabyloniancivilization.
�In the early 19th century opium extract was found to contain more
than20distinctcomplexorganicbases,calledalkaloids,ofwhichmorphine,
codeine, and papaverine are the most important. These
purealkaloidsreplacedcrudeopiumextractsintherapeutics.
MECHANISMOFACTION
�In the 1950s several new morphine like drugs
weredeveloped. Despite the increase in the number
ofcompoundsavailableforpainrelief,however,littlewasu
nderstoodof theirsitesandmechanisms ofaction.
ENKEPHALINS;
�The first real breakthrough came from the discovery,
byneuroscientistsJohnW.HughesandHansW.Kosterlitzatt
he University of Aberdeen in Scotland, of two
potentnaturally occurring analgesic Penta peptides
(peptidescontaining five linked amino acids) in extracts
of pigbrain. They called these compounds enkephalins,
andsincethenatleastsixmorehavebeenfound.
ENDORPHINS;
�Larger peptides, called endorphins, have been
isolated,andthesecontainsequencesofaminoacidsthatca
nbesplitoffasenkephalins.
TYPESOFRECEPTORS
�There are atleastthreetypesofreceptorson
brain neurons that are activated by the
enkephalins.Morphineanditscongeners
arethoughttoexerttheireffectsbyactivatingoneormore
ofthesereceptors.
�Painreliever;
USESOFOPIOIDDRUGS
Opioiddrugsareusefulinthetreatmentof
generalpostoperativepain,severepain,andotherspecificconditions.
Theuseof opioidstorelievethepainassociatedwithkidney
stonesorgallstonespresumablydependsontheirabilitytoaffectopioidrecept
orsinthesetissuesandtoinhibitcontractility.
�Reliefofrespiratorydistress;
�Low doses of opioids are also used for relief of the respiratory
distressthat accompanies acute cardiac insufficiency complicated by
thebuildupoffluidin thelungs.
CONTINUE…
Relieveabdominaldistress;
�Opioids are also able to relieve the abdominal distress and fluid
lossofdiarrhea.
�Usedindrugtherapeutics;
�Several commonly used natural or synthetic derivatives of morphine
areusedindrugtherapeutics.
�Codeine;
�Codeine, a naturally occurring opium alkaloid that can be
madesynthetically,isausefuloralanalgesic,especiallywhenusedin
combinationwith aspirin.
�Meperidine
CONTINUE…
Meperidine was an early synthetic analog of morphine, marketed
underthetradename Demerol,
thatwasoriginallythoughttobeabletoprovidesignificant short-lasting
analgesia and little or no addiction because of
itsshorteneddurationofaction;however,thisbeliefprovedfalse.
�Methadone;
Methadone, a synthetic opioid analgesic, has long-lasting
analgesiceffects(sixtoeighthours)when
takenorallyandisusedtomoderatetheeffectofwithdrawalfrom
heroinaddiction.
OPIOIDANTAGONISTDRUGS;
�Among the opioid antagonist drugs, naloxone and its longer-
lastingorally active version, naltrexone, are used primarily to
reversemorphine overdoses and to reverse the chemical stupor of a
widervariety of causes, including alcohol intoxication and anesthesia.
Inopioid overdoses, these drugs provide recovery within minutes
ofinjection. They can, however, also precipitate severe
withdrawalreactionsin apersonaddictedto opiates.
SIDE EFFECTS OF
NARCOTICANALGESICS
�Chestpain
�Troublebreathing(respiratory depression)
�Abnormalheartbeats
�Cardiacarrest
�Death
Narcoticsapplicationsindentistry;
�Narcotics analgesics are extremely effective in
reducingacutedentalandpostoperativepain
�The narcotics analgesics have established a niche for
thetreatment of pain in those situations where the
NSAIDsarelesseffective.
�Hydrocodone, oxycodone. Codeine and
occasionallymeperidinearethenarcoticsusedto
treatdentalpain.
�Vomiting
MORPHINE SIDEEFFECTS
�Respiratorydepression
�Decreasingofbloodpressure
�Sideeffectsofopioidanalgesics
�Respiratorydepression
�Euphoria
�Relaxationandsleep
�Tranquilization
�Decreasedbloodpressure
�Constipation
�Hypothermia
�Flushedandwarmedskin
SIDE EFFECTSOFANALGESIC
�Constipation.
�Drowsiness.
�Dizziness.
�Upsetstomach.
�Ringinginyourears.
�Skinitchingorrash.
�Drymouth.
�Aggravationofasthma
�Heartburn

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