Pain Flashcards
on what basis are opioids classified?
their actions are reversed by the opioid receptor antagonist naloxone
what type of pain are opioids used for? when are they not effective?
they’re used for mild - severe pain
but they cannot be used for neuropathic pain
what is spinal analgesia?
which opiate receptors are used?
spinal analgesia involves the the MU and delta opioid receptors.
opioid receptors are inhibitory- most of them are pre-synaptic:
- prevent neurotransmitter release at the C fibre nerve terminals
- they do this by opening potassium channels
the remaining post-synaptic receptors:
- prevent the generation of an AP by
- hyperporalsing dendrites of projection neurones, and interneurones and disinhibiting inhibitory neurones
why is complete C fibre inhibition not possible when nerve damage is associated?
in nerve damage:
- there is excessive NMDA firing, which is hard to inhibit
- CCK is immobilised in the spinal cord, which interferes with opiate action
pre-emptive analgesia, aid in the reduction of post operative pain by preventing the activations of these systems
what is supraspinal analgesia?
those involve nuclei in the brainstem and mid-brain
e.g.
locus corelus - producing noradrenaline
raphe nuclei - producing 5HT
periaqueductal grey - producing encephalin
those nuclei have opiate receptors, and thus they alter activity of the descending pathways from these zones to the level of the spinal cord
mechanism of action not known:
- blur pain sensation?
- turn off spinal cord transmission of pain?
list some of the drugs used in neuropathic pain
amitriptyline - used to inhibit Na and 5HT re-uptale
-actually an anti-depressant
gabapetine- calcium channel blocker (an anti -epileptic drug)
phenytoin and carbamazepine (used to stabilise membrane potential)
lidocaine (LA - used to stabilise membrane potential)
what are the CNS affects of opiates?
reduced sensitivity to PCo2 causes respiratory depression (most common cause of death)
activation of chemoreceptor trigger zone: causing nausea and vomitting
inhibition of reflex pathways due to opiate inhibition of brainstem nuclei: causes cough suppression
why does the use of opiate raise fear of addiction? why is that not the case?
opioids raise dopamine levels in the ventral tegmentum
they also raise noradrenaline levels and transmission in the locus coreulus
both sites are involved with the reward and dependance processes - but dependance does not occur in cases of pain
what is the difference between the Mu opioid receptors and the kappa/delta receptors!
kappa and delta - they’re associated with less respiratory depression
kappa no danger of dependance, but accompanied by aversion and non-rewards side-effects
what are the peripheral affects of opiates?
- constriction of GI smooth muscle causes constipation
- constriction of pupils, because they act on the oculmotor nucleus
- diminished propulsion coupled with their lack of secretion, causes an anti-dirroheal effect
- constricts all sphincters within the GI tract
- morphine can cause histamine release from mast cells (leading to bronchospasm and irritation, but only at very high concentrations)
- at therapeutic dosages, the opiate agonists do not have cardiovascular effect)
which receptor do all clinically significant opioid agonists work on?
give the name of three agonists?
what is the exception?
all significant ones act on Mu receptors
- codeine (weak opiate, orally effective)
- methadone (long duration, orally effective)
- fentanyl (very potent, short duration)
exception: pentazocine which acts on a kappa receptor
how do heroine and tramdol produce analgesia?
herione:
- very lipophilic, crosses the blood brain barrier
- in brain is metabolised to morphine
- acts on MU receptors
tramadol:
- only weak opiate actions
- prevents the reuptake of 5HT and NA
- thus producing analgesia
what is nalaxone? when is it used?
naloxone is a competitive antagonist at all three opioid receptors, but with the highest affinity to the mu receptor
used in cases of overdose, in particular to reverse respiratory depression.
antagonists used to probe the function of the opioid receptors
what role does inflammation play in peripheral sensitisation
inflammation causes the release of many mediators
prostaglandins - from membrane
bradykinin - from vasculature
5HT release
those act on C fibre nerve terminals at high concentration, activating the C fibres
they lower the threshold stimulus of nociceptors, so that they respond to lower stimulus
how is pain associated with inflammation treated, mainly?
using NSAIDs - those block prostanglandin production, but this has major affect in the GI system
cyclooxygenase inhibitors can also be used, with less marked GI side effects?
