Nocturnal hormone profiles in patients with schizophrenia treated with olanzapine

被引:64
作者
Mann, K
Rossbach, W
Müller, MJ
Müller-Siecheneder, F
Pott, T
Linde, I
Dittmann, RW
Hiemke, C
机构
[1] Johannes Gutenberg Univ Mainz, Dept Psychiat, D-55101 Mainz, Germany
[2] Lilly Deutschland GmbH, Homburg, Germany
[3] Univ Hamburg, Childrens Hosp, Psychosomat Dept, Hamburg, Germany
关键词
olanzapine; nocturnal hormone profiles; sleep EEG; schizophrenia;
D O I
10.1016/j.psyneuen.2005.08.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nocturnal hormone profiles were measured in patients with schizophrenia with predominantly negative symptoms both under drug-free baseline conditions and after subchronic administration of the atypical antipsychotic olanzapine, with the aim of characterizing its pharmacological properties on the neuroendocrine level. The following hormones were studied in the steep laboratory under polysomnographic control: adrenocorticotrophic hormone, cortisol, growth hormone (GH), prolactin, testosterone, and melatonin. Blood samples were taken at regular time intervals over the night, and serum concentrations of the hormones were determined. Ten patients completed the study, two of them were excluded from analysis due to incomplete hormone profiles. The dynamics of baseline nocturnal hormone secretion were similar to the patterns known from healthy subjects. After the treatment period of about 4 weeks, hypothalamic-pituitary-adrenal axis activity was reduced with decreased cortisol plasma levels compared to baseline conditions. Olanzapine induced a moderate prolactin elevation. The characteristic GH peak around steep onset, clearly present under baseline conditions, was markedly reduced after treatment. Testosterone and melatonin secretion were not significantly altered. In conclusion, although interpretation is difficult in some cases due to interference with indirect effects of olanzapine administration and the consequences of the clinical course of the underlying schizophrenic disorder, the neuroendocrine findings are consistent with the receptor-binding profile of olanzapine where, beside the D-2 antagonism, the antiserotonergic properties are most important. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:256 / 264
页数:9
相关论文
共 50 条
[1]   HPA axis and cytokines dysregulation in schizophrenia: potential implications for the antipsychotic treatment [J].
Altamura, AC ;
Boin, F ;
Maes, M .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 1999, 10 (01) :1-4
[2]  
[Anonymous], WILLIAMS TXB ENDOCRI
[3]   Pharmacokinetic-pharmacodynamic study of apomorphine's effect on growth hormone secretion in healthy subjects [J].
Aymard, G ;
Berlin, I ;
de Brettes, B ;
Diquet, B .
FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2003, 17 (04) :473-481
[4]   Effects of the antipsychotic drug sulpiride on reproductive hormones in healthy men: Relationship with body weight regulation [J].
Baptista, T ;
Alastre, T ;
Contreras, Q ;
Martinez, JL ;
de Baptista, EA ;
Paez, X ;
Hernandez, L .
PHARMACOPSYCHIATRY, 1997, 30 (06) :250-255
[5]   Dopamine as a prolactin (PRL) inhibitor [J].
Ben-Jonathan, N ;
Hnasko, R .
ENDOCRINE REVIEWS, 2001, 22 (06) :724-763
[6]   Olanzapine - An updated review of its use in the management of schizophrenia [J].
Bhana, N ;
Foster, RH ;
Olney, R ;
Plosker, GL .
DRUGS, 2001, 61 (01) :111-161
[7]   THE GONADAL AXIS IN MEN WITH SCHIZOPHRENIA [J].
BROWN, AS ;
HEMBREE, WC ;
FRIEDMAN, JH ;
KAUFMANN, CA ;
GORMAN, JM .
PSYCHIATRY RESEARCH, 1995, 57 (03) :231-239
[8]   Antagonism by olanzapine of dopamine D1, serotonin2, muscarinic, histamine H1 and α1,-adrenergic receptors in vitro [J].
Bymaster, FP ;
Nelson, DL ;
DeLapp, NW ;
Falcone, JF ;
Eckols, K ;
Truex, LL ;
Foreman, MM ;
Lucaites, VL ;
Calligaro, DO .
SCHIZOPHRENIA RESEARCH, 1999, 37 (01) :107-122
[9]   Radioreceptor binding profile of the atypical antipsychotic olanzapine [J].
Bymaster, FP ;
Calligaro, DO ;
Falcone, JF ;
Marsh, RD ;
Moore, NA ;
Tye, NC ;
Seeman, P ;
Wong, DT .
NEUROPSYCHOPHARMACOLOGY, 1996, 14 (02) :87-96
[10]  
Bymaster FP, 1997, J CLIN PSYCHIAT, V58, P28