Analgesic Drugs 1: Opiates and Opioids Flashcards
What sort of pain do opioids/opiates deal with?
Nociceptive and inflammatory pain
Possible ways of administering opioids
Orally
Parenteraly: intramuscular, intravenous
transmucosal
transdermal
Opiates vs opioids
Opiates are the narcotic analgesic derived from the opium plant naturally
Opioids are narcotic analgesics made synthetically, not found in nature
Commonly used opioids
Morphine; fentanyl; pethidine; codeine; methadone
Opioid receptors
Are presynaptic receptors that belong to the G protein coupled family of receptors.
Some post synaptic receptors
Mechanism of action of opioids
1) Activates G proteins causing inhibition of adenylate cyclase. This causes a decrease in Ca2+ channel permeability, so transmitters are not released
2) On post synaptic receptors, increase K+ conductance, causing hyperpolarisation, so a decreased response
What are the three kinds of opioid receptors?
Mu, kappa and delta found in the CNS
Mu-2 evokes a lot of responses (euphoria, analegesia)
Opioid receptor synthesis
Tissue damage occurs, causing the dorsal root ganglion to synthesise the receptors and place themselves along the axons
Opioid receptor agonists and antagonists, partial agonists
Agonists: morphine, pethidine, fentanyl but to different receptors at different affinities
Antagonists: Naloxone
partial agonists: bup re morphine
Adverse effects of opioids
Resp depression; drowsiness; constipation; nausea/vomiting; bradycardia, hypotension (morphine)
Natural opiates
Morphine and codeine
Semi-synthetic opioids
Bup-re-norphine
Heroin
Oxycodone
Synthetic opioids
Fentanyl
Pethidine
Methadone
tramadol
Endogenous opioids
endorphins (mu); endomorphins (mu); enkephalins; dynorphins
What are used to manage opioid withdrawal and some adjunctives
Metahodone and bup-re norphine with Clonidine (reduce autonomic response) promethazine for vomiting diazepam for muscle spasms anti diarrheal
OR rapid opiate detoxification, us of high doses of naltrexone under GA
Details about MORPHINE
dynamics and kinetics
eye?
note bioavailability 25%
Powerful analgesia
cough suppression
pin point pupil miosis
euphoria
Large volume of distribution (1/3 boud to plasma proteins)
3 hour half life
low lipid solubility (slow onset long duration)
Morphine metabolism
M3G
M6G which is potent analgesic, long half life
Pethidine details: side effects etc
bioavailability 50%
Synthetic
Tachycardia; dry mouth, miosis less marked
high lipid solubility so fats onset
Metabolism of pethidine note
Metabolism product norpethidine has a long half life and can cause renal failure, cause hallucinations and seizures
Fentanyl
High lipid sol. - fast onset
mu receptor agonist strong
80-100 times more potent.
Normally IV or transdermal patches
Methadone
Well absorbed from all routes oral is common
rapid onset of analgesia
no cognitive impairment or euphoria
Can be used for chronic pain and neuropathic pain due o NMDA receptor antagonism
Tramadol
Oral administration good
Inhibits uptake of noradrenaline and serotonin
Can cause serotonin syndrome in conjunction with other drugs suchs as SSRI’s
Nitrous oxide: preparation; onset; effects
Prep: entonox (half N2O and O2)in birth,wund dressing change
Powerful analgesic, rapid onset and offset
Euphoric; not addictive