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Effect of menstrual cycle phase on neuroendocrine and behavioral responses to the serotonin agonist m-chlorophenylpiperazine in women with premenstrual syndrome and controls.

Abstract
To evaluate the potential role of serotonin in the premenstrual syndrome (PMS), we investigated the effects of menstrual cycle phase on neuroendocrine and behavioral responses to the serotonergic agent m-chlorophenylpiperazine (m-CPP) in women with PMS and controls. A single oral dose of m-CPP (0.5 mg/kg) was administered to 10 PMS patients and 10 healthy controls during the follicular and luteal phases of the menstrual cycle. We observed the following. m-CPP administration during the luteal phase resulted in an acute improvement of PMS symptoms; the plasma cortisol and ACTH responses to m-CPP were blunted in both menstrual cycle phases in PMS patients compared with controls. These data provide evidence for the acute efficacy of m-CPP in the treatment of PMS. Although there is additional evidence for dysregulation of either the hypothalamic-pituitary-adrenal axis or serotonin control of the hypothalamic-pituitary-adrenal axis in women with PMS, there is little evidence for luteal phase-specific serotonergic dysfunction. These findings, nonetheless, implicate the serotonin system as a modulating (not causal) factor in PMS.
AuthorsT P Su, P J Schmidt, M Danaceau, D L Murphy, D R Rubinow
JournalThe Journal of clinical endocrinology and metabolism (J Clin Endocrinol Metab) Vol. 82 Issue 4 Pg. 1220-8 (Apr 1997) ISSN: 0021-972X [Print] United States
PMID9100599 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
Chemical References
  • Hormones
  • Piperazines
  • Serotonin Receptor Agonists
  • 1-(3-chlorophenyl)piperazine
Topics
  • Adult
  • Affect (drug effects)
  • Behavior (drug effects)
  • Female
  • Follicular Phase
  • Hormones (blood)
  • Humans
  • Luteal Phase
  • Menstrual Cycle
  • Neurosecretory Systems (drug effects)
  • Piperazines (blood, therapeutic use)
  • Premenstrual Syndrome (drug therapy, physiopathology, psychology)
  • Reference Values
  • Self Concept
  • Serotonin Receptor Agonists (pharmacology)

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