Smith.Ch3.Pain Flashcards
hyepralgesia deifnition
exaggerated responses to painful stimuli
allodynia
pain resulting from normally innocuous simtuli
In regards to pain management what are the regulations of the ELDU under AMDCUA
- ELDU is allowed only by or under the supervision of a veterinarian
- ELDU is allowed only for US food and drug Administration (FDA) approved animal and human drugs
- ELDU is only permitted when the health of the animal is threatened and not for production purposes
- ELDU in feed is prohibited
- ELDU is not permitted if it results in a violative drug residue in food intended for human consumption
Lidocaine has a rapid onset of activity in what time period?
and duration of action?
2 to 5 minutes onset of activity
90 minutes duration of action
NSAID produce analgesia an dantiinflammatory effects through which mechanism?
prostaglandin (PG) synteshsis through inhibition of enzyme cyclo-oxygenase (COX) in peripehra ltissues and centrla nervous system
COX-1 is expressed on what tissues?
peripheral and central nervous systems
**expression enhanced by pain and inflammatory mediators
COX-2 is expressed on what tissues?
ubiquitous in the CNS
– only becomes the major enzyme for PG syntehsis after induction by facotrs released during cell damage and death
What is the mean bioavailability of topical flunixin used in cattle?
48% (range: 34 to 61%)
What is the mean half life for topical flunixin?
6.42 hours (range 5.22 to 9.76 hours)
Phenylbutazone use is not approved for use in cattle because what effects have been seen in humans?
fatal bloo dsycrasias, including aplastic anemia, leukopenia, agranulocytosis, trhombocytopenia, deahts in humans
The analgesic effects of opioids are associated with binding to spinal and supraspinal:
mu
kappa
sigma receptors
The binding of opioids to respective receptors causes what:
decreased propagation of the nociceptive signal by activating receptor linked potassium channels and inhibiting voltage-gated calcium channels
MOA of ketamine
N-methylD aspartate (NMDA) receptor antagonist
Gabapentin MOA (suspected)
binds alpha2-delta subunit of voltage gated calcium channels acting presynaptically to decrease the release of excitatory neurotransmitters