Narcotic Analgesics Flashcards

1
Q

Opioids

A

Natural or synthetic morphine-like agents

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2
Q

Enkephalin Structure

A

Tyr-Gly-Gly-Phe- (Met/Leu)

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3
Q

Endorphins

A

30aa long- metenkephalin are last 5

Similar acting sites

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4
Q

Natural Opioids

A

Papaver Somniferum seed- morphine and codeine (3-methyl morphine)

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5
Q

Semi-Synthetic Opioid

A

Heroin (3,6 diacetyl morphine)

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6
Q

CNS Effects of Morphine

A
Dec. Pain perception- spinal effect
Inc. pain tolerance- supraspinal effect
Mood via Nucleus Acumbens- euphoria, dysphoria, restlesness
Sedation via locus coeruleus
Resp depression via medulla
N&V at CTZ
Miosis via occulomotor nuclei
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7
Q

Analgesic Effects of Opioids

A

Spinal- decreased ascending activity
Supraspinal- increased descending activity
Peripheral- opioid receptors expressed peripherally on chronic pain
Neuropathic- hyperalgesia & allodynia

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8
Q

Mu Opioid Receptors

A

Presynaptic inhibition: Dec. Ca influx
Postsynaptic inhibition: Inc. K influx
GPCR
Long-term: Activates MAP Kinase mediating physical dependence

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9
Q

GI Effects

A

Inc tone, dec. peristalsis
Delayed passage- increased water reabsorption
Constipation
Dec HCl secretion
Constriction of Sphincter of Oddi- increase bile pressure

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10
Q

Other Effects

A

Bronchoconstriction and vasodilation- increased histamine release
Urinary retention
Haemodynamic effects

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11
Q

Codeine

A

Weak agonist-no change in mood
1/10 analgesia of morphine
Antitussive at subanalgesic doses

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12
Q

Heroin

A

X3 analgesic potency of morphine
Easily passes through BBB
Hydrolysed to morphine and 6-monoacetylmorphine
Less emetic than morphine

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13
Q

Methadone

A
Slow onset, long duration >24 hours
Stabilise addicts
Cardiotoxicity risk
Oral or IV
Less euphoria
Attenuates withdrawal syndrome
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14
Q

Remifentanil

A
Ultra-short acting
Methyl ester hydrolysed by esterases
IV analgesia in minor surgery
Easily controlled
T1/2: 5 minutes
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15
Q

Naloxone

A
Competitive antagonist at all receptors
Short half-life: 30 minute duration
Precipitates withdrawal symptoms
Reduce stress-induced analgesia
Rapidly metabolised by liver
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16
Q

Methyl Naltrexone

A

Methyl group prevents BBB cross

Prevents CNS effects but peripheral antagonism at mu

17
Q

Morphine

A

Free OH on benzene ring bound to N
Active metabolite: morphine-6-glucoronide
Emetic

18
Q

Biased Agonism

A

Gi- therapeutic effects
B-Arrestin: down regulation
Oliceridine is selective for Gi and is in clinical trials

19
Q

Entero-hepatic Recirculation

A

Glucuronidated morphine excreted in bile
Gut flora remove glucuronide creating free morphine
Free morphine is reabsorbed causing a second peak

20
Q

Receptor Classes

A

All are GPCR’s
Mu- most analgesia
Delta- analgesia but pro-convulsant
Kappa- dynorphins bind- dysphoria. Pentazocine is a partial agonist
Functional heteromers occur creating diversity