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Effects of alpha-methyl-para-tyrosine-induced catecholamine depletion in patients with seasonal affective disorder in summer remission.

Abstract
Noradrenergic and dopaminergic mechanisms have been proposed for the pathophysiology of seasonal affective disorder (SAD). We investigated the effects of catecholamine depletion using alpha-methyl-para-tyrosine (AMPT), an inhibitor of tyrosine hydroxylase, in patients with SAD in natural summer remission. Nine drug-free patients with SAD by DSM-IV criteria, in summer remission for at least eight weeks, completed a double-blind, crossover study. Behavioral ratings and serum HVA and MHPG levels were obtained for 3-day sessions during which patients took AMPT or an active control drug, diphenhydramine. The active AMPT session significantly reduced serum levels of HVA and MHPG compared with the control diphenhydramine session. The AMPT session resulted in higher depression ratings with all nine patients having significant clinical relapse, compared with two patients during the diphenhydramine session. All patients returned to baseline scores after drug discontinuation. Catecholamine depletion results in significant clinical relapse in patients with SAD in the untreated, summer-remitted state. AMPT-induced depressive relapse may be a trait marker for SAD, and/or brain catecholamines may play a direct role in the pathogenesis of SAD.
AuthorsR W Lam, E M Tam, A Grewal, L N Yatham
JournalNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology (Neuropsychopharmacology) Vol. 25 Issue 5 Suppl Pg. S97-101 (Nov 2001) ISSN: 0893-133X [Print] England
PMID11682283 (Publication Type: Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Catecholamines
  • Enzyme Inhibitors
  • alpha-Methyltyrosine
  • Tyrosine 3-Monooxygenase
  • Dopamine
  • Norepinephrine
Topics
  • Affect (drug effects)
  • Catecholamines (deficiency)
  • Cross-Over Studies
  • Dopamine (blood, metabolism)
  • Double-Blind Method
  • Enzyme Inhibitors (pharmacology)
  • Female
  • Humans
  • Male
  • Norepinephrine (blood, metabolism)
  • Remission, Spontaneous
  • Seasonal Affective Disorder (chemically induced, physiopathology, psychology)
  • Seasons
  • Tyrosine 3-Monooxygenase (antagonists & inhibitors)
  • alpha-Methyltyrosine (pharmacology)

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