opioids Flashcards
Pain control can be provided by:
- local anesthetics
2. opioids
Most induction agents or inhaled agents
do not provide pain relief (ketamine provides a little pain relief)
Opiate
is the term used to designate drugs derived from opium
Opioid
refers to all substances natural (morphine) and synthetic (fentanyl) and semi-synthetic (heroin) that bind to opioid receptors and produce an agonist effect
Structure of opioids
- Phenanthrenes- morphine, codeine, thebaine
2. Benzylisoquinolones- (lack analgesic activity)- papaverine & noscapine
Opioid Classification
- naturally occurring
- semisynthetic
- synthetic
Naturally occurring opioid
Morphine
Semisynthetic opioids
analogs of morphine (difference in changing the structure slightly
- heroin
- hydromorphone
- codeine
Synthetic opioids
Exogenous (4 groups)
- Morphinan derivatives
- Diphenyl derivatives
- Benzomorphans
- Phenylpiperidines
Morphinan derivatives
- agonist-antagonists
1. Levorphenol
2. Butorphenol
Diphenyl derivatives
Methadone
Benzomorphans
- Phenazocine
- Pentazocine
* *used more for vasodilation than for pain
Phenylpiperidines
VERY COMMON IN THE OR
- Meperidine
- Fentanyl
- Alfentanil
- Sufentanil
- Remifentanil
Further classification of opioids
- agonist
- partial agonist (weaker drugs)
- buprenorphine: regardless of dose- can’t produce full mu receptor effects like morphine - 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 - Antagonist
- naloxone
Opiate Receptors
1973- researchers described the presence of receptors
1975- endogenous agonists were identified
1. enkephalins
2. endorphins
3. dynorphins
Opioid Receptors
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)
Mu receptor
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
Mu-1 receptor
Effects:
- Analgesia: supraspinal (mainly), spinal (lesser)
- Euphoria
- Miosis
- . Bradycardia
- Hypothermia
- Urinary retention
- Low abuse potential
Agonists: morphine, all endogenous, exogenous, synthetic opioids
Antagonists: naloxone, naltrexone, nalmefene
Mu-2 receptor
Effects:
- Analgesia: spinal analgesia
- hypoventilation
- MARKED constipation
- physical dependence
Agonists: morphine all endogenous, exogenous, synthetic opioids
Antagonists: naloxone, naltrexone, nalmefene
Kappa receptor
Effects:
- Analgesia: supraspinal and spinal (equally)
- Dysphoria
- Sedation
- Miosis
- Diuresis
- Low abuse potential
Agonists: Dynorphins
Antagonists: naloxone, naltrexone, nalmefene
Delta receptor
Effects:
- Analgesia: supraspinal and spinal (equally)
- Hypoventilation
- Urinary retention
- MINIMAL constipation
- Physical dependence
Agonists: Enkephalins
Antagonists: naloxone, naltrexone, nalmefene