Uptake and distribution of a new SSRI, NS2381, studied by PET in living porcine brain.

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Uptake and distribution of a new SSRI, NS2381, studied by PET in living porcine brain. / Smith, D F; Gee, A D; Hansen, Søren Baarsgaard; Moldt, P; Nielsen, E Ø; Scheel-Krüger, J; Gjedde, A.

In: European Neuropsychopharmacology, Vol. 9, No. 4, 1999, p. 351-9.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Smith, DF, Gee, AD, Hansen, SB, Moldt, P, Nielsen, EØ, Scheel-Krüger, J & Gjedde, A 1999, 'Uptake and distribution of a new SSRI, NS2381, studied by PET in living porcine brain.', European Neuropsychopharmacology, vol. 9, no. 4, pp. 351-9.

APA

Smith, D. F., Gee, A. D., Hansen, S. B., Moldt, P., Nielsen, E. Ø., Scheel-Krüger, J., & Gjedde, A. (1999). Uptake and distribution of a new SSRI, NS2381, studied by PET in living porcine brain. European Neuropsychopharmacology, 9(4), 351-9.

Vancouver

Smith DF, Gee AD, Hansen SB, Moldt P, Nielsen EØ, Scheel-Krüger J et al. Uptake and distribution of a new SSRI, NS2381, studied by PET in living porcine brain. European Neuropsychopharmacology. 1999;9(4):351-9.

Author

Smith, D F ; Gee, A D ; Hansen, Søren Baarsgaard ; Moldt, P ; Nielsen, E Ø ; Scheel-Krüger, J ; Gjedde, A. / Uptake and distribution of a new SSRI, NS2381, studied by PET in living porcine brain. In: European Neuropsychopharmacology. 1999 ; Vol. 9, No. 4. pp. 351-9.

Bibtex

@article{05f59800b31511debc73000ea68e967b,
title = "Uptake and distribution of a new SSRI, NS2381, studied by PET in living porcine brain.",
abstract = "This study tests the utility of a new selective serotonin reuptake inhibitor (SSRI), [11C]NS2381 {(+/-)-(8-[11C]methyl-3-(4-trifluoromethyl-phenyl)-8-azabicyclo[3.2.1]oc t-2-ene)}, as positron-emitting radioligand for labelling serotonin (5-HT) reuptake sites in living brain. Studies of monoamine uptake were carried out initially in vitro using rat brain synaptosomes. They showed that NS2381 and its precursor NS2435 are selective inhibitors of serotonin (5-HT) uptake. Then, studies were carried out in vivo on the uptake and distribution of [11C]NS2381 in living porcine brain. They showed that the radiotracer accumulates readily in brain, and binds reversibly in regions rich in serotonin uptake sites (e.g. raphe, basal ganglia and thalamus). In addition, [11C]NS2381 was displaced from brain tissue by the potent SSRI citalopram. The enantiomers of [11C]NS2381 were, in general, found to be similar to the racemate in terms of their uptake and distribution in living pig brain. Thus, [11C]NS2381 fulfilled several criteria of a PET radioligand for studying 5-HT uptake sites in the living brain.",
author = "Smith, {D F} and Gee, {A D} and Hansen, {S{\o}ren Baarsgaard} and P Moldt and Nielsen, {E {\O}} and J Scheel-Kr{\"u}ger and A Gjedde",
year = "1999",
language = "English",
volume = "9",
pages = "351--9",
journal = "European Neuropsychopharmacology",
issn = "0924-977X",
publisher = "Elsevier",
number = "4",

}

RIS

TY - JOUR

T1 - Uptake and distribution of a new SSRI, NS2381, studied by PET in living porcine brain.

AU - Smith, D F

AU - Gee, A D

AU - Hansen, Søren Baarsgaard

AU - Moldt, P

AU - Nielsen, E Ø

AU - Scheel-Krüger, J

AU - Gjedde, A

PY - 1999

Y1 - 1999

N2 - This study tests the utility of a new selective serotonin reuptake inhibitor (SSRI), [11C]NS2381 {(+/-)-(8-[11C]methyl-3-(4-trifluoromethyl-phenyl)-8-azabicyclo[3.2.1]oc t-2-ene)}, as positron-emitting radioligand for labelling serotonin (5-HT) reuptake sites in living brain. Studies of monoamine uptake were carried out initially in vitro using rat brain synaptosomes. They showed that NS2381 and its precursor NS2435 are selective inhibitors of serotonin (5-HT) uptake. Then, studies were carried out in vivo on the uptake and distribution of [11C]NS2381 in living porcine brain. They showed that the radiotracer accumulates readily in brain, and binds reversibly in regions rich in serotonin uptake sites (e.g. raphe, basal ganglia and thalamus). In addition, [11C]NS2381 was displaced from brain tissue by the potent SSRI citalopram. The enantiomers of [11C]NS2381 were, in general, found to be similar to the racemate in terms of their uptake and distribution in living pig brain. Thus, [11C]NS2381 fulfilled several criteria of a PET radioligand for studying 5-HT uptake sites in the living brain.

AB - This study tests the utility of a new selective serotonin reuptake inhibitor (SSRI), [11C]NS2381 {(+/-)-(8-[11C]methyl-3-(4-trifluoromethyl-phenyl)-8-azabicyclo[3.2.1]oc t-2-ene)}, as positron-emitting radioligand for labelling serotonin (5-HT) reuptake sites in living brain. Studies of monoamine uptake were carried out initially in vitro using rat brain synaptosomes. They showed that NS2381 and its precursor NS2435 are selective inhibitors of serotonin (5-HT) uptake. Then, studies were carried out in vivo on the uptake and distribution of [11C]NS2381 in living porcine brain. They showed that the radiotracer accumulates readily in brain, and binds reversibly in regions rich in serotonin uptake sites (e.g. raphe, basal ganglia and thalamus). In addition, [11C]NS2381 was displaced from brain tissue by the potent SSRI citalopram. The enantiomers of [11C]NS2381 were, in general, found to be similar to the racemate in terms of their uptake and distribution in living pig brain. Thus, [11C]NS2381 fulfilled several criteria of a PET radioligand for studying 5-HT uptake sites in the living brain.

M3 - Journal article

C2 - 10422897

VL - 9

SP - 351

EP - 359

JO - European Neuropsychopharmacology

JF - European Neuropsychopharmacology

SN - 0924-977X

IS - 4

ER -

ID: 14943513