Analyses of [18F]altanserin bolus injection PET data. II: Consideration of radiolabeled metabolites in humans
@article{Price2001AnalysesO,
title={Analyses of [18F]altanserin bolus injection PET data. II: Consideration of radiolabeled metabolites in humans},
author={Julie C. Price and Brian J Lopresti and Carolyn C. Meltzer and G. S. Smith and Neale S. Mason and Y. Huang and Daniel P. Holt and Roger N. Gunn and Chester A. Mathis},
journal={Synapse},
year={2001},
volume={41}
}Imaging serotonin‐2A (5‐HT2A) neuroreceptors with positron emission tomography (PET) and [18F]altanserin has been the focus of a series of PET studies, as [18F]altanserin is one of the most selective 5‐HT2A antagonist radiotracers. Previous animal studies showed that radiolabeled metabolites (radiometabolites) of [18F]altanserin crossed the blood–brain barrier (BBB) to localize nonspecifically in brain, consistent with a constant radioactivity “background.” In this work, we evaluated human…
60 Citations
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References
SHOWING 1-10 OF 73 REFERENCES
Analyses of [18F]altanserin bolus injection PET data. I: Consideration of radiolabeled metabolites in baboons
- BiologySynapse
- 2001
After bolus injection in baboons, two of the major radiometabolites of [18F]altanserin crossed the BBB and contributed to a fairly uniform background of nonspecific radioactivity, which suggests that conventional analyses are appropriate for human bolus injections [18 F]altanerin PET data, although these methods may overestimate [18f]altANSerin nonspecial binding.
[18F]Altanserin PET Studies of Serotonin-2A Binding: Examination of Nonspecific Component
- Biology, Chemistry
- 1998
CHAPTER 44 – Characterization of the Radiolabeled Metabolites of [18F]Altanserin: Implications for Kinetic Modeling
- Biology, Chemistry
- 1998
PET quantification of 5-HT2A receptors in the human brain: a constant infusion paradigm with [18F]altanserin.
- BiologyJournal of nuclear medicine : official publication, Society of Nuclear Medicine
- 2000
The results demonstrate the feasibility of equilibrium imaging with [18F]altanserin over more than 5 radioactive half-lives and suggest a method to overcome difficulties associated with lipophilic radiolabeled metabolites.
Characterization of radioactive metabolites of 5-HT2A receptor PET ligand [18F]altanserin in human and rodent.
- Chemistry, BiologyNuclear medicine and biology
- 1999
Kinetics and Modeling of l-6-[18F]Fluoro-DOPA in Human Positron Emission Tomographic Studies
- Biology, ChemistryJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism
- 1991
Results showed that a model consisting of three separate compartments for tissue FDOPA, tissue 6-[18F]fluorodopamine (FDA) and its metabolites, and tissue l-3,4-dihydroxy-6-[18f]fluoro-3-O-methylphenylalanine (3-OMFD) could describe adequately the striatal kinetics in humans.
Serotonin 5HT2 Receptor Imaging in the Human Brain Using Positron Emission Tomography and a New Radioligand, [18F]Altanserin: Results in Young Normal Controls
- Biology, ChemistryJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism
- 1995
The results suggest that [18F]altanserin is selective for S2 receptors in vivo as it is in vitro, and indicate that it is suitable for imaging and quantifying S1 receptors with PET in humans.
Fluorine-18-altanserin: a radioligand for the study of serotonin receptors with PET: radiolabeling and in vivo biologic behavior in rats.
- Biology, ChemistryJournal of nuclear medicine : official publication, Society of Nuclear Medicine
- 1991
This radiopharmaceutical appears to be more selective for S2 receptor sites than other ligands available today and allows the study of S2 receptors under in vivo conditions.
Test–retest variability of serotonin 5‐HT2A receptor binding measured with positron emission tomography and [18F]altanserin in the human brain
- BiologySynapse
- 1998
Results demonstrate that the test–retest variability of [18F]altanserin‐specific binding is comparable to that of other PET radiotracers and that the regional specific binding of [ 18F]ALTanser in human brain was correlated with the known regional distribution of 5‐HT2A receptors.
Visualisation of loss of 5-HT2A receptors with age in healthy volunteers using [18F]altanserin and positron emission tomographic imaging
- Biology, MedicinePsychiatry Research: Neuroimaging
- 1996