Chapter 7; Nervous System and Euthanasia Flashcards
Anticonvulsant Drugs: Barbiturates
Depresses the motor centres of the cerebral cortex
Controlled substance
Long-acting: 6-8 hours - phenobarbital
Short-acting: 1-2 hours - pentobarbital
Ultrashort-acting: 10-15 minutes - thiopental methohexital
Anticonvulsant Drugs: Barbiturates
phenobarbital
Long-acting; 6-8 hours
Dogs and cats
Highly protein bound
CYP450 inducer
liquid or tablet
side effects; PU, PD, PP (polyphagia), liver damage
Anticonvulsant Drugs: Benzodiazepines
Enhances GABA which is an inhibitory neutotransmitter
Controlled substance
Side effect: sedation
Anticonvulsant Drugs: Benzodiazepines
diazepam
Emergency drug given IV or rectally to conrtol status epilepticus
Anticonvulsant Drugs: Potassium Bromide
Combintation with phenobarbitol or forst line drug
Enhances GABA
Liquid
Serum monitoring needed
Side effect: vomiting, sedation
DO NOT USE WITH CATS - allgeric bronchitis
Anticonvulsant Drugs: Add-Ons
levetriacetam
Binds to synaptic vesicle protein and prevents conduction of impulses across the synapse
Liquid or tablet
Side effect: sedation, ataxia
Anticonvulsant Drugs: Add-Ons
gabapentin
Inhibits calcium channels
Excreted by kidney - kidney disease
tablet
Side effect: sedation, ataxia
Narcotic Analgesics: Opioids
Mimic action of andogenous opioids produced in nervous and endocrine system
Complex interaction at opioid recptors: mu, kappa, and delta
Activity in central areas of brain, GI tract, smooth muscle
Side effect: sedation, vomiting, salivation, ileus, slowed HR and hypotension
Morphine is the opioid to which all other opioids are compared
Narcotic Analgesics: Opioids
fentanyl
200X
IV as CRI (IM, SC) (q 2 hours)
transdermal patch (3 days)
full mu agonist
Narcotic Analgesics: Opioids
hydromorphone
5-7X
IV, IM, SC (q 4-6 hours)
full mu agonist
Narcotic Analgesics: Opioids
butorphanol
2-5X
IV, IM, SC (short duration 1-2 hours)
partial mu agonist
pre-anaesthetic sedation/analgesia
Narcotic Analgesics: Opioids
buprenorphine
30X
IM (q 8-10 hours)
transmucousal (q 12 hours)
SC slow release (depot) (q 72 hours)
mu agonist
used for post-surgical anaglesia
few side effects
Narcotic Analgesics: Opioids
naloxone
Full mu antagonist
strong affinity for receptor but has no activity st receptor site
opioid reveral agent
Narcotic Analgesics: Opioid?
tramadol
IV, IM or oral (q 8-12 hours)
partial mu agonist
inhibits reuptake of serotonin and NE
post-operative and chronic pain managment
Local Anesthetics
Block sensory and pain transmission at site of application - prevent nerve impluse conduction in peripheral nerves
Possible side effect: seizures, arrythmias