opioids Flashcards

1
Q

Pain control can be provided by:

A
  1. local anesthetics

2. opioids

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2
Q

Most induction agents or inhaled agents

A

do not provide pain relief (ketamine provides a little pain relief)

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3
Q

Opiate

A

is the term used to designate drugs derived from opium

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4
Q

Opioid

A

refers to all substances natural (morphine) and synthetic (fentanyl) and semi-synthetic (heroin) that bind to opioid receptors and produce an agonist effect

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5
Q

Structure of opioids

A
  1. Phenanthrenes- morphine, codeine, thebaine

2. Benzylisoquinolones- (lack analgesic activity)- papaverine & noscapine

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6
Q

Opioid Classification

A
  1. naturally occurring
  2. semisynthetic
  3. synthetic
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7
Q

Naturally occurring opioid

A

Morphine

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8
Q

Semisynthetic opioids

A

analogs of morphine (difference in changing the structure slightly

  1. heroin
  2. hydromorphone
  3. codeine
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9
Q

Synthetic opioids

A

Exogenous (4 groups)

  1. Morphinan derivatives
  2. Diphenyl derivatives
  3. Benzomorphans
  4. Phenylpiperidines
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10
Q

Morphinan derivatives

A
  • agonist-antagonists
    1. Levorphenol
    2. Butorphenol
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11
Q

Diphenyl derivatives

A

Methadone

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12
Q

Benzomorphans

A
  1. Phenazocine
  2. Pentazocine
    * *used more for vasodilation than for pain
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13
Q

Phenylpiperidines

A

VERY COMMON IN THE OR

  1. Meperidine
  2. Fentanyl
  3. Alfentanil
  4. Sufentanil
  5. Remifentanil
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14
Q

Further classification of opioids

A
  1. agonist
  2. partial agonist (weaker drugs)
    - buprenorphine: regardless of dose- can’t produce full mu receptor effects like morphine
  3. Mixed agonist/antagonist (much better option that antagonist when reversing)
    - nalbuphine- agonist at kappa receptor and antagonist at mu receptor= reverses respiratory depression while still acting on kappa
  4. Antagonist
    - naloxone
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15
Q

Opiate Receptors

A

1973- researchers described the presence of receptors
1975- endogenous agonists were identified
1. enkephalins
2. endorphins
3. dynorphins

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16
Q

Opioid Receptors

A

1980s- existence of opioid receptor and began naming them (mu, kappa, delta)— most drugs aren’t specific and work all of the receptors

  • believed that synthetic opioids mimic action of endogenous opioids by binding to the opioid receptors
  • when binding occurs= activation of pain modulating systems in brain and spinal cord
  • *antinociceptive- inhibits excitatory neurotransmitters (is substance P)
17
Q

Mu receptor

A

There are 2 subtypes (mu-1 and mu-2)
Mu-3 are thought to be involved in the immune process

ALL ENDOGENOUS AND EXOGENOUS AGONISTS ACT ON MU RECEPTORS
-mu receptors are primarily in the brain and spinal cord

18
Q

Mu-1 receptor

A

Effects:

  1. Analgesia: supraspinal (mainly), spinal (lesser)
  2. Euphoria
  3. Miosis
  4. . Bradycardia
  5. Hypothermia
  6. Urinary retention
  7. Low abuse potential

Agonists: morphine, all endogenous, exogenous, synthetic opioids
Antagonists: naloxone, naltrexone, nalmefene

19
Q

Mu-2 receptor

A

Effects:

  1. Analgesia: spinal analgesia
  2. hypoventilation
  3. MARKED constipation
  4. physical dependence

Agonists: morphine all endogenous, exogenous, synthetic opioids
Antagonists: naloxone, naltrexone, nalmefene

20
Q

Kappa receptor

A

Effects:

  1. Analgesia: supraspinal and spinal (equally)
  2. Dysphoria
  3. Sedation
  4. Miosis
  5. Diuresis
  6. Low abuse potential

Agonists: Dynorphins
Antagonists: naloxone, naltrexone, nalmefene

21
Q

Delta receptor

A

Effects:

  1. Analgesia: supraspinal and spinal (equally)
  2. Hypoventilation
  3. Urinary retention
  4. MINIMAL constipation
  5. Physical dependence

Agonists: Enkephalins
Antagonists: naloxone, naltrexone, nalmefene