Literature DB >> 7669486

Influence of the dosing interval on prolactin release after remoxipride.

G Movin-Osswald1, M Hammarlund-Udenaes, C Von Bahr, P Eneroth, K Walton-Bowen.   

Abstract

1. The prolactin response following administration of the D2-dopamine receptor antagonist remoxipride was studied in eight healthy male volunteers. The purpose of the study was to investigate the duration of a refractory period of prolactin release following two doses of remoxipride. A further aim was to compare the prolactin response following remoxipride and thyrotropin release hormone (TRH) during the refractory period. The subjects received two 30 min intravenous (i.v.) infusions of remoxipride 50 mg with different time intervals between the two doses, in a randomized six period crossover design. The time intervals between the two remoxipride doses were 2, 8, 12, 24 and 48 h. On one occasion the remoxipride dose was followed by an i.v. injection of TRH after 2 h. 2. The plasma peak prolactin concentrations obtained after the first remoxipride dose correspond to a maximal release of prolactin according to earlier studies. A small second peak of prolactin was observed after 2 h. The release was gradually increased with longer time intervals between the consecutive doses. The refractory period for a second prolactin release similar to the first one after remoxipride was found to be 24 h for most of the subjects. 3. TRH resulted in a faster and higher increase in prolactin response of a shorter duration than after remoxipride administered 2 h after the first dose.

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Year:  1995        PMID: 7669486      PMCID: PMC1365057          DOI: 10.1111/j.1365-2125.1995.tb04487.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  33 in total

Review 1.  The regulation of prolactin secretion in humans.

Authors:  A G Frantz
Journal:  Front Neuroendocrinol       Date:  1973       Impact factor: 8.606

Review 2.  Drug-induced changes in prolactin secretion. Clinical implications.

Authors:  K Hell; H Wernze
Journal:  Med Toxicol Adverse Drug Exp       Date:  1988 Nov-Dec

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Authors:  G Movin-Osswald; M Hammarlund-Udenaes
Journal:  Br J Clin Pharmacol       Date:  1991-09       Impact factor: 4.335

4.  Neuroendocrine responses to single oral doses of remoxipride and sulpiride in healthy female and male volunteers.

Authors:  C von Bahr; F A Wiesel; G Movin; P Eneroth; P Jansson; L Nilsson; S Ogenstad
Journal:  Psychopharmacology (Berl)       Date:  1991       Impact factor: 4.530

5.  Differential prolactin responses to haloperidol and TRH in normal adult men.

Authors:  S E Hays; R T Rubin
Journal:  Psychoneuroendocrinology       Date:  1981       Impact factor: 4.905

6.  Remoxipride in schizophrenia: effects on plasma prolactin.

Authors:  G Chouinard; L Turnier; M A Kallai-Sanfacon
Journal:  Prog Neuropsychopharmacol Biol Psychiatry       Date:  1985       Impact factor: 5.067

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Authors:  M E McMurdo; P W Howie; M Lewis; M Marnie; J McEwen; A S McNeilly
Journal:  Br J Clin Pharmacol       Date:  1987-08       Impact factor: 4.335

8.  Remoxipride, a new potential antipsychotic compound with selective antidopaminergic actions in the rat brain.

Authors:  S O Ogren; H Hall; C Köhler; O Magnusson; L O Lindbom; K Angeby; L Florvall
Journal:  Eur J Pharmacol       Date:  1984-07-20       Impact factor: 4.432

9.  A controlled dose-ranging study of remoxipride and haloperidol in schizophrenia--a Canadian multicentre trial.

Authors:  Y D Lapierre; N P Nair; G Chouinard; A G Awad; B Saxena; B Jones; D J McClure; D Bakish; P Max; R Manchanda
Journal:  Acta Psychiatr Scand Suppl       Date:  1990

10.  Safety evaluation in both short- and long-term treatment of schizophrenia with remoxipride.

Authors:  D Morrison; A Englund; V Lawrie; T Lewander; A Schlachet; S E Westerbergh
Journal:  Acta Psychiatr Scand Suppl       Date:  1990
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