5-HT1A receptor imaging in the human brain:: Effect of tryptophan depletion and infusion on [18F]MPPF binding

被引:34
作者
De Haes, JIU
Bosker, FJ
Van Waarde, A
Pruim, J
Willemsen, ATM
Vaalburg, W
Den Boer, JA
机构
[1] Univ Groningen Hosp, Dept Biol Psychiat, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen Hosp, PET Ctr, NL-9700 RB Groningen, Netherlands
关键词
PET; 5-HT1A receptor; serotonin; F-18]MPPF; intrasynaptic; extrasynaptic; affinity;
D O I
10.1002/syn.10134
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The 5-HT1A receptor has been implicated in a variety of physiological processes, psychiatric disorders, and neurodegenerative disorders. [F-18]MPPF is a useful radioligand for quantitative imaging of 5-HT1A receptors in human subjects. Previous studies have shown that the binding of some radioligands is sensitive to changes in neurotransmitter concentration, whereas in other cases, binding is not affected. In the present study we investigated if [F-18]MPPF binding to the 5-HT1A receptor is sensitive to changes in 5-HT. Changes in 5-HT levels were achieved by influencing its synthesis through tryptophan depletion, including a tryptophan-free amino acid drink 4.5 h prior to the PET scan and tryptophan infusion (10 mg/ml, 50 mg/kg, 30 min, starting 60 min prior to the PET scan). Binding of [F-18]MPPF in the brain of six healthy, male volunteers was compared in these two conditions. Mean binding potentials in the medial temporal cortex, cortical regions, and raphe nucleus did not significantly differ between the two conditions. The results of the study show that, under the experimental conditions used, [F-18]MPPF binding was not affected. It is hypothesized that the increases in 5-HT levels needed to produce a measurable effect on [F-18]MPPF binding would be significantly greater than that possible with tryptophan manipulation. Therefore, in pathological conditions, where such large increases in 5-HT levels are not expected, [F-18]MPPF seems a useful ligand to measure 5-HT1A receptor distribution without the interference of endogenous 5-HT. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:108 / 115
页数:8
相关论文
共 52 条
[21]  
Kema IP, 2001, CLIN CHEM, V47, P1811
[22]   QUANTITATIVE AUTORADIOGRAPHIC CHARACTERIZATION OF THE BINDING OF [H-3] WAY-100635, A SELECTIVE 5-HT1A RECEPTOR ANTAGONIST [J].
KHAWAJA, X .
BRAIN RESEARCH, 1995, 673 (02) :217-225
[23]  
KHAWAJA X, 1995, J NEUROCHEM, V64, P2716
[24]  
Larisch R, 2000, J NUCL MED, V41, p135P
[25]   Imaging synaptic neurotransmission with in vivo binding competition techniques:: A critical review [J].
Laruelle, M .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2000, 20 (03) :423-451
[26]   High-yield radiosynthesis and preliminary in vivo evaluation of p-[18F]MPPF, a fluoro analog of WAY-100635 [J].
Le Bars, D ;
Lemaire, C ;
Ginovart, N ;
Plenevaux, A ;
Aerts, J ;
Brihaye, C ;
Hassoun, W ;
Leviel, V ;
Mekhsian, P ;
Weissmann, D ;
Pujol, JF ;
Luxen, A ;
Comar, D .
NUCLEAR MEDICINE AND BIOLOGY, 1998, 25 (04) :343-350
[27]   In vivo binding properties of [carbonyl-11C]WAY-100635:: Effect of endogenous serotonin [J].
Maeda, J ;
Suhara, T ;
Ogawa, M ;
Okauchi, T ;
Kawabe, K ;
Zhang, MR ;
Semba, J ;
Suzuki, K .
SYNAPSE, 2001, 40 (02) :122-129
[28]  
McNair D. MM., 1971, Manual for the Profile of Mood States (POMS)
[29]   DOSE-RESPONSE DECREASE IN PLASMA TRYPTOPHAN AND IN BRAIN TRYPTOPHAN AND SEROTONIN AFTER TRYPTOPHAN-FREE AMINO-ACID MIXTURES IN RATS [J].
MOJA, EA ;
CIPOLLA, P ;
CASTOLDI, D ;
TOFANETTI, O .
LIFE SCIENCES, 1989, 44 (14) :971-976
[30]   FURTHER EVIDENCE FOR DIFFERENTIAL AFFINITY STATES OF THE SEROTONIN-1A RECEPTOR IN RAT HIPPOCAMPUS [J].
MONGEAU, R ;
WELNER, SA ;
QUIRION, R ;
SURANYICADOTTE, BE .
BRAIN RESEARCH, 1992, 590 (1-2) :229-238