Premium
Inverse changes in raphe and cortical 5‐HT 1B receptor availability after acute tryptophan depletion in healthy human subjects
Author(s) -
Baldassarri Stephen R.,
Park Eunkyung,
Finnema Sjoerd J.,
Planeta Beata,
Nabulsi Nabeel,
Najafzadeh Soheila,
Ropchan Jim,
Huang Yiyun,
Hannestad Jonas,
Maloney Kathleen,
Bhagwagar Zubin,
Carson Richard E.
Publication year - 2020
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/syn.22159
Subject(s) - serotonergic , raphe nuclei , raphe , radioligand , serotonin , binding potential , medicine , endocrinology , chemistry , median raphe nucleus , tryptophan , dorsal raphe nucleus , receptor , amino acid , biochemistry
Serotonergic neurotransmission plays a key role in the pathophysiology and treatment of various neuropsychiatric diseases. The purpose of this study was to investigate changes in serotonergic neurotransmission after acute tryptophan depletion (ATD) using positron emission tomography (PET) with [ 11 C]P943, a 5‐HT 1B receptor radioligand previously shown to be sensitive to changes in 5‐HT. Five healthy subjects were scanned on a high resolution PET scanner twice on the same day, before and approximately 5 hours after ingesting capsules containing an amino acid mixture that lacks tryptophan. For each scan, emission data were acquired for 120 min after intravenous bolus injection of [ 11 C]P943. Binding potential ( BP ND ) values were estimated from parametric images using the second version of the multilinear reference tissue model (MRTM2, t * = 20 min) with cerebellar grey matter used as a reference region. The change in [ 11 C]P943 binding (Δ BP ND , %) was calculated as ( BP ND,post − BP ND,pre )/( BP ND,pre ) × 100, and correlation analysis was performed to measure linear associations of Δ BP ND between raphe and other regions of interest (ROIs). Δ BP ND ranged from −6% to 45% in the raphe, with positive values indicating reduced competition from 5‐HT. In cortical regions, Δ BP ND ranged from −28% to 7%. While these changes did not reach significance, there were significant negative correlations of Δ BP ND of the raphe with those of cerebral cortical regions and the thalamus (e.g., r = −.96, p = .011 for average cortex). These findings support the hypothesis that raphe serotonin is a critical modulator of cortical serotonin release via projecting neurons in healthy human subjects.