(08) Narcotic Analgesics Flashcards

1
Q
  1. What is a useful and inexpensive analgesic and sedative, used widely along in dogs?
  2. selective or no?
  3. can it be used orally?

why?

A
  1. morphine
  2. non-selective opiod agonist
  3. no

highly metabolized during its first pass through liver and trapped in the stomach of animals who have highly acidic gastric fluids

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2
Q
  1. What is a potent analgesic agent by its interaction with kappa receptors?
  2. How relative to morphine (potency, deficiency)?
  3. more or less respiratoy/gi depressant effects than morphine?
  4. What else can it do?
A
  1. Butorphanol
  2. It is a long acting narcotic analgesic that is 4-7 times more potent than morphine but less efficacious.
  3. Used clinically, it produces fewer respiratory depressant and GI effects than morphine
  4. Butorphanol may be useful to reverse a morphine-induced respiratory depression but still provide some analgesia
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3
Q
  1. What 3. Nalorphine is a partial narcotic analgesic agonist that is inexpensive an a sufficiently weak agonist that it is used to reverse opioid activity?
  2. Unfortunately it also has enough agonistic activity that it can induce what at high doses?
  3. The respiratory depressant effect of nalorphine can be antagonized by what?
A
  1. nalorphine
  2. respiratory depression (so readministration should be done with caution)
  3. naloxone
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4
Q
  1. What is a pure optiod antagonist?
  2. . It is relatively non-selective and expensive - does it have respiratory depressant effect?
  3. . It is short acting, so how much you administer?
A
  1. naloxone
  2. no
  3. so it must be readministered frequently until the opioid agonist has worn off.
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5
Q
  1. What is an opiate that is about 10 times more potent than morphine,?
  2. more or less

respiratory depression

sedation

A
  1. oxymorphone
  2. less

more

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6
Q
  1. What is a potent (about 100-150 times) more potent than morphine—and short acting opioid agonist
  2. usually mixed with what as a neuroleptoanalgesic mixture?
  3. It is usually coadministred with what?
A
  1. Fentanyl
  2. major tranquillizers
  3. droperidol
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7
Q
  1. Can The antitussive effect of an opiod agonist be reversed by an opioid antagonist?
A
  1. no
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8
Q
  1. Do opiate antagonists and partial agonists stimulate receptors maximally?
  2. Compared to either butorphanol or fentanyl, diprenorphine has the more or least analgesic efficiacy.
A
  1. no
  2. least
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9
Q
    1. Opiates reduce neuronal transmission by doing what?
  1. Opiate analgesic drugs alleviate pain by doing what?
A
  1. opening neuronal K channels
  2. decreasing neurotransmitter release from pain transmitting neurons in spinal cord and brain.
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10
Q
    1. Morphine decreases propulsive movements of what?
A
  1. intestine and clamp sphincters
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11
Q
    1. Morphine is a useful analgesic in horses if its administration is preceded by a large dose of what?
A
  1. an appropriate sedative, such as xylazine
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12
Q
  1. What is a weak narctoic analgesic (1/3 morphine’s potency) use for equine colic?
  2. agonist of what?
  3. can also decrease the analgesic actions of what?
  4. It may even precipitate withdrawal in highly dependant individuals
  5. Its sigma activity results in what?
A
  1. pentazocrine
  2. kappa
  3. of B-endorphin that are mediated by mu-opioid receptors
  4. dysphoria
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