Comparison of the effects of citalopram and escitalopram on 5-Ht-mediated neuroendocrine responses

被引:37
作者
Nadeem, HS [1 ]
Attenburrow, MJ [1 ]
Cowen, PJ [1 ]
机构
[1] Univ Oxford, Warneford Hosp, Dept Psychiat, Oxford OX3 7JX, England
基金
英国医学研究理事会;
关键词
citalopram; escitalopram; saliva; cortisol; serotonin;
D O I
10.1038/sj.npp.1300475
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Acute oral administration of selective serotonin re-uptake inhibitors (SSRIs) increases plasma cortisol by facilitating brain serotonin activity. Recently, salivary cortisol sampling has grown in popularity as a noninvasive means of assessing HPA axis activity. The aim of the present study was to find out whether acute oral administration of the SSRI, citalopram, increases salivary cortisol in healthy volunteers and whether the increase produced by an equivalent dose of its active isomer, escitalopram, is greater. A total of 15 healthy subjects were tested on three occasions receiving either oral citalopram ( 20 mg), escitalopram ( 10 mg), or placebo in a double-blind, randomized, crossover design. Salivary cortisol and plasma cortisol and prolactin were measured for 240 min after each treatment. Relative to placebo, both citalopram and escitalopram increased salivary and plasma cortisol levels with no evidence of consistent differences between them. Plasma prolactin concentration was not altered by either active treatment. Plasma and salivary cortisol responses after citalopram but not escitalopram correlated significantly. The present study does not support an enhanced effect of escitalopram on 5-HT-mediated neuroendocrine responses.
引用
收藏
页码:1699 / 1703
页数:5
相关论文
共 22 条
  • [1] Attenburrow MJ, 2001, PSYCHOPHARMACOLOGY, V155, P323
  • [2] Acute citalopram administration produces correlated increases in plasma and salivary cortisol
    Bhagwagar, Z
    Hafizi, S
    Cowen, PJ
    [J]. PSYCHOPHARMACOLOGY, 2002, 163 (01) : 118 - 120
  • [3] Acute changes in cerebrospinal fluid 5-HIAA following oral paroxetine challenge in healthy humans
    Carpenter, LL
    Anderson, GM
    Siniscalchi, JM
    Chappell, PB
    Price, LH
    [J]. NEUROPSYCHOPHARMACOLOGY, 2003, 28 (02) : 339 - 347
  • [4] CLEMENT EM, 2001, J PSYCHOPHARMACOL S, V15, pA64
  • [5] Changes in plasma prolactin during SSRI treatment: evidence for a delayed increase in 5-HT neurotransmission
    Cowen, PJ
    Sargent, PA
    [J]. JOURNAL OF PSYCHOPHARMACOLOGY, 1997, 11 (04) : 345 - 348
  • [6] Central serotonergic effects of m-chlorophenylpiperazine (mCPP) among normal control adolescents
    Ghaziuddin, N
    Welch, K
    Greden, J
    [J]. NEUROPSYCHOPHARMACOLOGY, 2003, 28 (01) : 133 - 139
  • [7] Efficacy Comparison of Escitalopram and Citalopram in the Treatment of Major Depressive Disorder: Pooled Analysis of Placebo-Controlled Trials
    Gorman, Jack M.
    Korotzer, Andrew
    Su, Guojin
    [J]. CNS SPECTRUMS, 2002, 7 (04) : 40 - 44
  • [8] Pharmacokinetic comparison of oral solution and tablet formulations of citalopram: A single-dose, randomized, crossover study
    Gutierrez, MM
    Abramowitz, W
    [J]. CLINICAL THERAPEUTICS, 2000, 22 (12) : 1525 - 1532
  • [9] Oral application of citalopram (20 mg) and its usefulness for neuroendocrine challenge tests
    Hennig, J
    Netter, P
    [J]. INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2002, 5 (01) : 67 - 71
  • [10] Paroxetine as a 5-HT neuroendocrine probe
    Kojima, H
    Terao, T
    Iwakawa, M
    Soya, A
    Inoue, N
    Shiraishi, Y
    Son, Y
    Soeda, S
    Ueda, N
    Yoshimura, R
    Nakamura, J
    [J]. PSYCHOPHARMACOLOGY, 2003, 167 (01) : 97 - 102