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Norzimelidine, a metabolite of a highly selective 5-hydroxytryptamine uptake inhibitor, can inhibit the uptake of noradrenaline in-vivo.

Abstract
Zimelidine and norzimelidine were tested for their ability to counteract reserpine (2.5 mg kg-1)- or apomorphine (1-16 mg kg-1)-induced hypothermia and to potentiate TRH (40 mg kg-1)-induced hyperthermia in mice. Norzimelidine produced positive results in all three tests, behaving like a weak NA uptake inhibitor. Zimelidine was practically inactive. We conclude that the weak inhibitory effect of norzimelidine on the uptake of NA (in-vitro experiments) may be of importance for its pharmacological action and for the clinical action of zimelidine.
AuthorsL Pawłowski, H Mazela
JournalThe Journal of pharmacy and pharmacology (J Pharm Pharmacol) Vol. 36 Issue 12 Pg. 855-8 (Dec 1984) ISSN: 0022-3573 [Print] England
PMID6151986 (Publication Type: Journal Article)
Chemical References
  • Antidepressive Agents
  • Propylamines
  • Citalopram
  • Zimeldine
  • norzimelidine
  • Thyrotropin-Releasing Hormone
  • Reserpine
  • Apomorphine
  • Norepinephrine
Topics
  • Animals
  • Antidepressive Agents (pharmacology)
  • Apomorphine (pharmacology)
  • Body Temperature (drug effects)
  • Citalopram
  • Male
  • Mice
  • Norepinephrine (metabolism)
  • Propylamines (pharmacology)
  • Reserpine (pharmacology)
  • Thyrotropin-Releasing Hormone (pharmacology)
  • Zimeldine (analogs & derivatives, pharmacology)

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