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Nociception
Neural processing of noxious stimuli
Nociceptors
Another term for pain receptors
F; receptors also are located peripherally
True or False: Opiate receptors are only centrally located
Threshold
This must be reached before nocieptors trigger a signal
F: endogenous opioids occur
True or False: Opioid receptors respond only to exogenous compounds
Opium
The first opioid important into the US
Opium poppy
The sourece of opiates
Narcotics
An alternative term for opioids because of their ability to induced sleep
Opiates are "natural"; opioids also include synthetics, but all bind opioid receptors
The difference between opioids and opiates
Mu
The receptors responsible for euphoria characteristic of opioids
Mu, Kappa
The two primary opioid receptors targeted for control of analgesia
Mu, Kappa (agonist)
Receptors targeted by morphine, fentanly and oxymorphone
Mu (antagonist), Kappa (agonist)
Targeted by butorphanol
Naloxone
A "pure" mu opioid antagonist
Butorphanol
A "mixed" mu opioid antagonist
Buprenorphine
A "partial" mu opioid agonist
cAMP inhibited
The secondary messenger system for opioid receptors and how it is affected
G-proteins
Opioid rectpors are coupled to this
Inhibited release (also serotonin, substance P)
Opioid receptors stimulation has this effect on acetylcholine and dopamine
Decrease sensitivity to CO2
Opioids cause respiratory depression because of this effect
Constipation
Opioids have this effect on the gastrointestinal tract
Stimulation
Opioids generally have this effect on the emetic center
Apomorphine
An opioid used to induce emesis when appropriate for toxin ingestion
First pass metabolism
The reason that many opioids can not be given orally
Constant rate infusion
Some opioids are given via this route and method because of their short half-life
Fentanyl
An opioid available in a transdermal delivery system
Fentanyl
The most potent of the model opioids
Oxymorphone
A pure mu agonist approved for use in dogs and cats
Short eliminatinon half-life
A reason that fentanyl is administered as a transdermal patch
12 to 24 hours
The approximate time to onset of fentanyl when adminsitered as a transdermal patch
Horses, cows, cats
Species for which opioids may cause dysphoria rather than euphoria
Butorphanol and buprenorphine
This drug has very high affinity for Mu receptors and as such, is not easily reversed
Butorphanol
This drug can be used to reverse the effects of opioids at mu receptors while maintaining some analgesic effects
Buprenorphine
This opioid in general has a longer duration of action than most because of its tight affinity for mu receptors
Half-life is shorter than the agent being reversed
Why does naloxone administration generally have to be repeated when reversing opoids
Class II
The DEA schedule for fentanyl and morphine
Class III
The DEA schedule for buprenorphine
Class IV
The DEA schedule for butorphanol
Drug Enforcement or DEA
The agency other than the FDA that regulates opioids