Measurement of the serotonin 1A receptor availability in patients with schizophrenia during treatment with the antipsychotic medication ziprasidone

被引:8
作者
Frankle, W. Gordon [1 ,2 ]
Lombardo, Ilise [3 ]
Kegeles, Lawrence S. [1 ,2 ]
Slifstein, Mark [1 ,2 ]
Martin, John H. [2 ,4 ]
Huang, Yiyun [1 ,2 ,5 ]
Hwang, Dah-Ren [1 ,2 ,5 ]
Reich, Elisa [1 ,2 ]
Cangiano, Claudine [1 ,2 ]
Gil, Roberto [1 ,2 ]
Abi-Dargham, Anissa [1 ,2 ,5 ]
Laruelle, Marc [1 ,2 ,5 ,6 ,7 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Psychiat, New York, NY USA
[2] New York State Psychiat Inst & Hosp, New York, NY 10032 USA
[3] Pfizer Inc, New York, NY USA
[4] Columbia Univ, Coll Phys & Surg, Ctr Neurobiol & Behav, New York, NY USA
[5] Columbia Univ, Coll Phys & Surg, Dept Radiol, New York, NY USA
[6] GlaxoSmithKline Inc, Neurosci Ctr Excellence Drug Discovery, Schizophrenia & Cognit Disorder Discovery Perform, Harlow, Essex, England
[7] Univ London Imperial Coll Sci Technol & Med, Dept Neurosci, London, England
关键词
(11)C]WAY 100635; 5-HT1A receptor; PET; schizophrenia; ziprasidone; POSITRON-EMISSION-TOMOGRAPHY; 5-HT1A RECEPTOR; HUMAN-BRAIN; PREFRONTAL CORTEX; IN-VIVO; AUTORADIOGRAPHIC LOCALIZATION; DOPAMINE RELEASE; PARTIAL AGONIST; DRUG-ACTION; BINDING;
D O I
10.1177/0269881110388329
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The aim of this study was to compare 5-HT(1A) availability in vivo in individuals with schizophrenia before and during treatment with the atypical antipsychotic ziprasidone. Six individuals with schizophrenia underwent two PET scans with [(11)C]WAY 100635; the first while medication-free (baseline) and the second while taking the atypical antipsychotic ziprasidone (on-medication). Regional volumes of distribution (V(T), mL g(-1)) were derived using a two-tissue compartment kinetic model. Outcome measures included binding potential relative to the plasma (BP(P), mL g(-1)) and the binding potential relative to the nonspecific distribution volume (BP(ND), unitless). No significant differences were observed in regional BP(P) or BP(ND) with ziprasidone treatment. A significant correlation was noted between BP(P) measured in the orbitofrontal cortex during the on-medication condition and degree of improvement in negative symptoms with treatment (r = 0.96, p = 0.004). Consistent with the published literature of changes in 5-HT(1A) binding during treatment with 5-HT(1A) receptor agonists, this study did not detect a significant reduction in 5-HT(1A) binding with ziprasidone. The finding of a relationship between 5-HT(1A) binding and the degree of improvement in negative symptoms provides further support for the role of the 5-HT(1A) receptor in the pathophysiology and treatment of this symptom domain.
引用
收藏
页码:734 / 743
页数:10
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