Acute hormonal changes after IV citalopram and treatment response in OCD

被引:4
作者
Corregiari, Fabio M.
Gattaz, Wagner F.
Bernik, Marcio
机构
[1] Univ Sao Paulo, Hosp Clin, Fac Med, Inst Psiquiatria,Ambulatorio Ansiedade, Sao Paulo, Brazil
[2] Univ Sao Paulo, Hosp Clin, Fac Med, Inst Psiquiatria, Sao Paulo, Brazil
[3] Univ Sao Paulo, Hosp Clin, Fac Med, Inst Psiquiatria,Lab Neurociencias,LIM 27, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
obsessive-compulsive disorder; serotonin; prolactin; cortisol; growth hormone; therapeutic response; serotonin reuptake inhibitors; prognosys; citalopram;
D O I
10.1007/s00213-007-0793-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale Serotonergic pharmacological challenges have failed to produce consensual results in patients with obsessive-compulsive disorder (OCD), suggesting a heterogeneous 5-hydroxytryptamine (5-HT) activity in this disorder. Objectives The aim of this study was to compare the neuroendocrine response to a serotonergic challenge in OCD patient responders (RP) and nonresponders (NR) to serotonin reuptake inhibitors treatment and healthy volunteers. Materials and methods Thirty OCD treatment NR, 30 RP, and 30 controls (CN) matched for sex and age were included. Each subject received 20 mg of intravenous citalopram. Prolactin, cortisol, and growth hormone plasma concentration were measured at times-20, 0, 20, 40, 60, 80, 100, 120, 140, and 160 min after the onset of citalopram infusion. Results Citalopram did not induce anxiety or OCD symptoms in patients. Citalopram was associated with stronger prolactin response in the CN group (maximal percentage variation [max%Delta]=65.76 +/- 105.1) than in NR (max%Delta=17.41 +/- 31.06) and RP groups (max%Delta=15.87 +/- 31.71; p=0.032; Friedman chi(2)=6.87; df=2). On the other hand, cortisol response did not differ between CN and RP groups and was blunted in the NR group (NR max%Delta=20.98 +/- 58.14 vs RP max%Delta=47.69 +/- 66.94; CN max%Delta=63.58 +/- 88.4; p=0.015; Friedman chi(2)=8.60; d=2). Conclusion Compared to CN, both treatment RP and NR patients showed blunted prolactin response to citalopram, but only NR patients showed an attenuated cortisol response, suggesting a more disrupted central serotonergic transmission in this group.
引用
收藏
页码:487 / 494
页数:8
相关论文
共 28 条
[1]   Patients with obsessive-compulsive disorder have increased 5-HT2A receptor binding in the caudate nuclei [J].
Adams, KH ;
Hansen, ES ;
Pinborg, LH ;
Hasselbalch, SG ;
Svarer, C ;
Holm, S ;
Bolwig, TG ;
Knudsen, GM .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2005, 8 (03) :391-401
[2]  
Attenburrow MJ, 2001, PSYCHOPHARMACOLOGY, V155, P323
[3]   Opposite effects of antidepressants and corticosterone on the sensitivity of hippocampal CA1 neurons to 5-HT1A and 5-HT4 receptor activation [J].
Bijak, M ;
Zahorodna, A ;
Tokarski, K .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2001, 363 (05) :491-498
[4]  
CHARNEY DS, 1988, ARCH GEN PSYCHIAT, V45, P177
[5]   MCPP-induced hyperactivity in 5-HT2c receptor mutant mice is mediated by activation of multiple 5-HT receptor subtypes [J].
Dalton, GL ;
Lee, MD ;
Kennett, GA ;
Dourish, CT ;
Clifton, PG .
NEUROPHARMACOLOGY, 2004, 46 (05) :663-671
[6]   Pharmacotherapy of obsessive-compulsive disorder and obsessive-compulsive spectrum disorders [J].
Denys, Damiaan .
PSYCHIATRIC CLINICS OF NORTH AMERICA, 2006, 29 (02) :553-+
[7]   Effects of chronic antidepressants and electroconvulsive shock on serotonergic neurotransmission in the rat hypothalamus [J].
Dremencov, E ;
Gur, E ;
Lerer, B ;
Newman, ME .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2002, 26 (06) :1029-1034
[8]   Brain 5-HT function in obsessive-compulsive disorder - Prolactin responses to d-fenfluramine [J].
Fineberg, NA ;
Roberts, A ;
Montgomery, SA ;
Cowen, PJ .
BRITISH JOURNAL OF PSYCHIATRY, 1997, 171 :280-282
[9]   A comparison of d,l-fenfluramine and citalopram challenges in healthy adults [J].
Flory, JD ;
Manuck, SB ;
Perel, JM ;
Muldoon, MF .
PSYCHOPHARMACOLOGY, 2004, 174 (03) :376-380
[10]   Serotonin, the periaqueductal gray and panic [J].
Graeff, FG .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2004, 28 (03) :239-259