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Abstract
The effect of an initial challenge with the serotonin (5-HT) uptake inhibitor clomipramine
(CMI) on subsequent rechallenge was studied in healthy men who served as volunteers.
Carefully screened volunteers were assigned to one of three conditions: (1) CMI challenge
followed 2 weeks later by CMI rechallenge; (2) placebo challenge followed 2 weeks
later by CMI challenge; and (3) CMI challenge followed 4 weeks later by CMI rechallenge.
We found significant blunting of the prolactin response to CMI rechallenge 2 weeks
(Signed Rank = −12, p = 0.05), but not 4 weeks after an initial challenge. Placebo
challenge did not affect CMI challenge 2 weeks later. These findings suggest that
a single exposure to IV CMI may cause 5-HT receptor changes that are present 2, but
not 4 weeks later. The ramifications of this finding with regard to the use of 5-HT
challenge paradigms in a test-retest design are discussed.
Keywords
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References
- Amitriptyline sensitization of a serotonin-mediated behavior depends on the passage of time and not repeated treatment.Life Sci. 1983; 33: 1727-1730
- One stressful event blocks multiple actions of diazepam for up to at least a month.Brain Res. 1988; 445: 380-385
- Repeated tricyclics induce a progressive dopamine autoreceptor subsensitivity independent of daily drug treatment.Nature. 1980; 287: 451-454
- Efficacy of odansetron (GR 38032F) and the role of serotonin in cisplatin-induced nausea and vomiting.N Engl J Med. 1990; 322: 810-815
- Neuroendocrine effects of intravenous clomipramine in depressed patients and health subjects.Am J Psychiatry. 1992; 149: 1168-1175
- Abnormal neuroendocrine responsivity to acute i.v. clomipramine challenge in depressed patients.Psychiatry Res. 1990; 31: 39-47
- The effects of intravenous clomipramine on neurohormones in normal subjects.J Clin Endocrinol. 1989; 68: 632-637
- Comparison of growth hormone and prolactin stimulation induced by chlorimioramine and desipramine in man in connection with chlorimipramine metabolims.Psychopharmacology. 1984; 82: 62-67
- cortical B-adrenergic subsensitivity after desmethylimipramine may depend on the passage of time rather than daily treatment.Brain Res. 1983; 278: 359-361
- 3H-imipramine binding and 3H-5-HT uptake in human blood platelets: Changes after one week chlormipramine treatment.Eur J Pharmacology. 1984; 106 (1984): 629-633
- Acute antidepressant effect following pulse loading with intravenous and oral clomipramine.Arch Gen Psychiatry. 1989; 46: 29-35
- The schedule for affective Disorders and Schizophrenia.3rd ed. New York State Psychiatric Institute, New York1978
- Test-retest reliability of the prolactin and cortical response to D,L-fenfluramine challenge in dispruptive behavior disorders.Psychiatry Res. 1992; 42: 65-72
- Neuroendocrine aspects of the serotonergic hypothesis of depression.Neurosci Behav Rev. 1989; 13: 237-246
Article info
Publication history
Received in revised form:
August 5,
1993
Received:
June 11,
1992
Footnotes
☆Presented in part at the 47th Annual Meeting of the Society for Biological Psychiatry, Washington DC, April 30, 1992.
☆☆This research was supported in part by NIMH grants MH-42145, MH-19111, (MH-33127, and by NIH grant RR00046. Intravenous clomipramine (Anafranil) was provided by Ciba-Geigy.
Identification
Copyright
© 1993 Published by Elsevier Inc.