Pharmacology · MU Sofia

36. Opioid analgesics.

Covers opioids, from their natural, semi-synthetic and synthetic classes through to their mu-receptor action and reward-system effects. It then goes through routes of administration, lipophilicity and albumin binding, liver metabolism by CYP3A4 and CYP2D6, and half-lives of common agents such as morphine, fentanyl and methadone. Side effects, a list of drug interactions, therapeutic uses and risks in pregnancy and lactation close the note, followed by a short set of recap questions.

Inside: 1 section · 4 labelled pictures · 10 flashcards · 4 min

Topic 35 of 93 in the MU Sofia syllabus for Pharmacology (Medicine, Year 3). The free AceMed note covers it in 1 section, about 580 words (4 min of reading), with 10 flashcards.

In this note

  1. Opioids

Opioids

Opioids are a class of drugs that include natural, synthetic, and semi-synthetic compounds derived from the opium poppy plant or synthesized to mimic the action of natural opiates. These drugs are primarily used for pain relief but have the potential for abuse and addiction due to their effects on the brain's reward system.

Classification

Natural Opioids:

  • Morphine
  • Codeine

Semi-Synthetic Opioids:

  • Oxycodone
  • Hydrocodone
  • Heroin

Synthetic Opioids:

  • Fentanyl
  • Methadone
  • Tramadol
  • Pethidine

Pharmacodynamics

Opioids work by binding to opioid receptors in the central nervous system (CNS) and peripheral nervous system. The mu-opioid receptor is primarily involved in pain relief, and its activation leads to:

  • Inhibition of pain signal transmission
  • Altered pain perception
  • Production of feelings of euphoria

Additionally, opioids affect the brain's reward system, which leads to well-being and pleasure but also contributes to their potential for abuse and addiction.

Pharmacokinetics

Opioids can be administered via different routes:

  • Oral (common for chronic pain management)
  • Intravenous (IV), Intramuscular (IM), Subcutaneous (SC) (for acute pain)
  • Transdermal patches (for sustained release in chronic pain)
  • Rectal (when oral administration is not possible)

Absorption and Distribution:

  • Opioids are lipophilic, allowing them to cross the blood-brain barrier effectively.
  • They are widely distributed throughout the body, including the CNS.
  • They are plasma protein-bound, primarily to albumin, influencing their distribution and half-life.

Metabolism:

  • Most opioids are metabolized in the liver by cytochrome P450 enzymes, particularly CYP3A4 and CYP2D6.

Half-life of Common Opioids:

  • Morphine: 2-4 hours
  • Hydrocodone: 3-5 hours
  • Fentanyl: 3-12 hours (with transdermal system providing sustained release over 72 hours)
  • Methadone: 8-59 hours (long half-life supports its use in opioid dependence treatment)

Excretion: Opioids and their metabolites are primarily excreted by the kidneys via urine.

Side Effects

Common Side Effects:

  • Nausea, vomiting, constipation, drowsiness, dizziness, dry mouth

Severe Side Effects:

  • Respiratory depression, tolerance, dependence, addiction, overdose, and death

Drug Interactions

  • CNS depressants (e.g., benzodiazepines, alcohol): Increases the risk of respiratory depression and sedation.
  • CYP3A4 inhibitors (e.g., ketoconazole): Increase opioid levels, leading to toxicity.
  • CYP3A4 inducers (e.g., rifampin): Reduce opioid efficacy.
  • CYP2D6 inhibitors (e.g., fluoxetine): Lower the conversion of prodrugs like codeine, reducing pain relief.
  • Combining opioids with monoamine oxidase inhibitors (MAOIs) can cause severe reactions, including serotonin syndrome.
  • Serotonergic drugs (e.g., SSRIs) increase the risk of serotonin syndrome.
  • Anticholinergics (e.g., diphenhydramine): Enhance constipation and CNS depression.
  • Diuretics: Reduced effectiveness due to opioid-induced fluid retention.
  • Antiretrovirals: Alter opioid levels, requiring dose adjustments.
  • Anticonvulsants (e.g., gabapentin): Increase sedation and respiratory depression.

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