Opiates Flashcards
Define acute pain
short term with easily identifiable cause- warning of damage or disease by body, has physio purpose
Define chronic pain
persists longer than should, constant or intermittent but outlives purpose
Name 5 types of pain
Acute, chronic, neuropathic, visceral, somatic
Nociception
ability to perceive pain
Analgesia
loss of sensitivity to pain without loss of consciousness
Hyperalgesia
Increased response to painful stimuli when tissue already damaged
Allodynia
Pain caused by stim that wouldnt normally cause
Physio changes in pain (5)
CV (increased symp), HPA stress response, hyperglycemia (increased glycogenolysis), ileus (reduced GI), reduced immune function (wound healing)
What drugs are antitussive
Codeine and butorphanol
What drug is an emetic
hydromorphone
Three types of analgesics
Block transduction, block trasmission in sensory nerves, block/change transmission in spinal pathways (perception)
Which analgesic drugs block transduction
NSAIDs
Which analgesic drugs block transmission
Locals
Which analgesic drugs block spinal transmission/alter perception
Opioids, A2Agonsits, NMDAs, NSAIDs, locals
A2Agonists, NMDAs and opioids all work on ____ sites of action
CNS and spinal
Cannabinoids work at what site of action
CNS
NSAIDS work at what sites of action
Spinal cord and peripheral
What are the three receptors
delta, kappa, mu (OP1,2,3)
What is the ceiling effect
Dose at which no effects can be produced anymore
Receptors, which do dogs have many of? which do horses have many of?
Dogs- mu, horses- K
What systems are effected by the pharmacological actions of opioids
CNS (analgesia, mood, sedation, RR, nausea/vomiting), GI- constipation; CV- bradycardia, hypotension
Describe the effect of opioid analgesia at teh spinal cord
Hyperpolarization of neural cells via increased K activity
What are the two levels of action of CNS analgesia
Spinal cord- modulation of substance P and supraspinal decreased affective pain response (fear/anxiety)
Which receptor provides the most analgesia
mu
Which species experience myosis
dogs, primates
Which species experience mydriasis
small ruminants, cows, horses
How is ventilation depressed in opioid analgesia
Depressed PCO2 sensitivity in brainstem
How can ventilatory depression be reversed
Naloxone
What can reverse CV effects of opioids
Anti-cholinergic agents (to increase HR and BP)
What receptors does morphine act on
Mu- full agonist
Describe solubility and BBB of morphine
Low lipid solubility, low BBB
Morphine- metabolism
Glucuronic conjugation into M6G and M3G
Why is morphine less effective in cats
Less glucuronidation
What is the potency 1 prototype for all opioid receptor classes
Morphine
Side effects- morphine
Vomiting
Butorphanol- type
Agonist-antagonist (K, mu)
What drug can preserve analgesia and still reverse mu agonists
Butorphanol (k-ag, mu-antag)
What drug is best for patients with cardiac or respiratory issues
Butorphanol - less CV and respiratory depression
What drug is best in horses and ruminants
Butorphanol
What type of drug is buprenorphine
Partial mu agonist
Level of analgesia- morphine
moderate to high
Level of analgesia- butorphanol
mild
Level of analgesia- buprenorphine
mild to moderate
Advantages of buprenorphine
High bioavailability
What type of drug is naloxone
Full antagonist
Fentanyl - type
Opioid agonist
Fentanyl- potency
100x more than morphine (dosing 100x less)
Better CV drug - morphine or fentanyl - why
Fentanyl bc less histamine release
Meperidine- type
mu agonist
What drug is best in geriatric and young patients
Meperidine
What drug is the only opioid to cause increased HR
Meperidine ( like atropine)
Describe neuroleptanalgesia
Combination of analgesic with sedative (ex. alpha-2 agonist with phenothiazines)
Which drug has a short half life compared to others
Naloxone