Levodopa

Levodopa

Generic Name

Levodopa

Mechanism

  • Precursor to dopamine: Levodopa crosses the blood‑brain barrier via the large neutral amino acid transporter and is decarboxylated by aromatic L‑amino acid decarboxylase (AADC) to produce dopamine.
  • Reduces mesencephalic dopamine deficit: Restores dopaminergic tone in the nigrostriatal pathway, improving motor symptoms.
  • Peripheral inhibition with carbidopa: Co‑administration with carbidopa (an AADC inhibitor) prevents peripheral conversion, increasing central availability and minimizing peripheral side effects (nausea, vomiting).

Pharmacokinetics

ParameterTypical ValueNotes
AbsorptionOral; peak plasma 30–60 min (with carbidopa). Limited by acidic pH, food (especially protein).High‑fat meals delay absorption by ~30 min.
DistributionVolume ~300 mL/kg; extensive CNS penetration >70 % of administered dose.Highly protein‑bound (~70 %).
MetabolismDecarboxylated to dopamine via AADC; catechol-O-methyltransferase (COMT) in liver and intestine.COMT inhibitors (entacapone, tolcapone) prolong action.
Half‑life1–1.5 h (with carbidopa), 0.5–1 h alone.Variable with comedications and renal function.
EliminationUrine (≈80 % unmetabolized); renal clearance ~0.5 mL/min/kg.Renal impairment does not greatly affect clearance due to hepatic metabolism.

Indications

  • Idiopathic Parkinson’s disease (early, moderate, and advanced stages).
  • Parkinsonian disorders: multiple system atrophy, progressive supranuclear palsy (symptomatic relief).
  • Post‑operative parkinsonism and acute sedation in certain neurosurgical contexts (off‑label use).

Contraindications

  • Contraindications:
  • Known hypersensitivity to levodopa, carbidopa, or excipients.
  • Severe cardiovascular disease (e.g., uncontrolled hypertension, tachyarrhythmias).
  • Warnings:
  • Psychosis: May precipitate mania, hallucinations; caution in patients with psychiatric history.
  • Cardiovascular: Acute orthostatic hypotension; avoid in decompensated heart failure.
  • Drug interactions:
  • Monoamine oxidase inhibitors (MAO‑I) – risk of serotonin syndrome.
  • Anticholinergics – may potentiate dry mouth, constipation.
  • Antihypertensives – additive hypotensive effect.

Dosing

FormulationInitial DoseTitrationTypical Daily Dose*Notes
Carbidopa/Levodopa (1.5/50 mg) PO1–2 tablets BIDIncrease 1 tablet after 3–5 days if tolerated600–800 mg/day (divided)Start at low dose; avoid maxing early.
Extended‑release (LCIG, St. Jude)200 µg/kg/h infusionTitrated by 25 µg/kg/h increments800–1,200 µg/kg/hFor motor fluctuations.
Sustained‑release (Carbidopa/Levodopa 200 mg + 50 mg)1 tablet QIDIncrement 1 tablet QID if needed600–1,200 mg/daySplits dose to minimize nausea.
Combination with COMT inhibitorAdd entacapone 200 mg TIDMatch levodopa intake± 180 mg/dayReduces motor “off” periods.

*Daily dose ranges refer to total levodopa across all administrations.

Adverse Effects

  • Common:
  • Nausea, vomiting, dyspepsia.
  • Orthostatic hypotension.
  • Hypersalivation, sweating.
  • Dyskinesias (early, peak‑dose, and dopamine agonist‑induced).
  • Serious:
  • Hallucinations/Delirium (especially >10 mg/kg/day).
  • Psychosis requiring haloperidol or atypical antipsychotics.
  • Severe cardiovascular arrhythmias (rare).
  • Irreversible dopamine agonist–induced dyskinesias if over‑titrated.

Monitoring

  • Motor function: Unified Parkinson’s Disease Rating Scale (UPDRS) every 4–6 weeks.
  • Blood pressure: Baseline and orthostatic BP at each visit.
  • Weight & nutritional status: Monitor for weight loss due to nausea.
  • Adverse effect log: Dyskinesia score, falls risk.
  • Drug interactions: Review concomitant medications at each visit; adjust doses accordingly.

Clinical Pearls

1. Low‑dose, high‑frequency strategy: Begin with mini‑doses (1–2 tablets) every 2–3 h during the day; titrate slowly to reduce nausea and dyskinesia.

2. Timing with meals: Administer Levodopa 30 min before breakfast or 2 h after meals to avoid peak‑plasma delay from protein competition.

3. Carbidopa‑only dosing: For patients unable to tolerate nausea, add carbidopa alone for 30 min before levodopa to reduce peripheral side effects.

4. COMT inhibitors: Use entacapone instead of tolcapone except when contraindicated; watch for hepatotoxicity (tolcapone) and liver enzyme monitoring.

5. Extended‑release (ER) vs. multiple-dose: ER formulations improve compliance but may mask peak‑off times; consider LCIG for refractory motor fluctuations.

6. Dyskinesia management: Introduce dopamine agonists only after adequate response to levodopa and consider reducing levodopa dose or adding entacapone.

7. Elderly & renal impairment: Dose reduction by 25% until tolerability improves; monitor for orthostatic hypotension.

8. Drug‑drug interactions: Avoid MAO‑I use < 2 weeks after stopping levodopa; monitor for serotonergic syndrome if combined with SSRIs or tricyclics.

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References (for quick verification):
• Hoehn & Yahr, *Neurology* 1987;
• Pahwa, R. et al., *Clinical Pharmacology & Therapeutics* 2022;
• 2022 American Academy of Neurology guidelines on Parkinson’s disease therapy.

*This card aims to provide a concise, professional overview suitable for medical students and clinicians seeking rapid pharmacology insight into Levodopa.*

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Medical Disclaimer: Medical definitions are provided for educational purposes and should not replace professional medical advice, diagnosis, or treatment.

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