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… 
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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
TLDR
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
PET quantification of 5-HT2A receptors in the human brain: a constant infusion paradigm with [18F]altanserin.
TLDR
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.
Kinetics and Modeling of l-6-[18F]Fluoro-DOPA in Human Positron Emission Tomographic Studies
  • S. Huang, D. Yu, +6 authors M. Phelps
  • Biology, Chemistry
    Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism
  • 1991
TLDR
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
  • B. Sadzot, C. Lemaire, +8 authors G. Franck
  • Biology, Chemistry
    Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism
  • 1995
TLDR
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.
TLDR
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
TLDR
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
...
1
2
3
4
5
...