Influx of a choline analog to dog brain measured by positron emission tomography.

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Influx of a choline analog to dog brain measured by positron emission tomography. / Redies, C; Diksic, M; Collier, B; Gjedde, A; Thompson, C J; Gauthier, S; Feindel, W H.

In: Synapse, Vol. 2, No. 4, 1988, p. 406-11.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Redies, C, Diksic, M, Collier, B, Gjedde, A, Thompson, CJ, Gauthier, S & Feindel, WH 1988, 'Influx of a choline analog to dog brain measured by positron emission tomography.', Synapse, vol. 2, no. 4, pp. 406-11. https://doi.org/10.1002/syn.890020407

APA

Redies, C., Diksic, M., Collier, B., Gjedde, A., Thompson, C. J., Gauthier, S., & Feindel, W. H. (1988). Influx of a choline analog to dog brain measured by positron emission tomography. Synapse, 2(4), 406-11. https://doi.org/10.1002/syn.890020407

Vancouver

Redies C, Diksic M, Collier B, Gjedde A, Thompson CJ, Gauthier S et al. Influx of a choline analog to dog brain measured by positron emission tomography. Synapse. 1988;2(4):406-11. https://doi.org/10.1002/syn.890020407

Author

Redies, C ; Diksic, M ; Collier, B ; Gjedde, A ; Thompson, C J ; Gauthier, S ; Feindel, W H. / Influx of a choline analog to dog brain measured by positron emission tomography. In: Synapse. 1988 ; Vol. 2, No. 4. pp. 406-11.

Bibtex

@article{2b1a1bb0b31511debc73000ea68e967b,
title = "Influx of a choline analog to dog brain measured by positron emission tomography.",
abstract = "The influx of the 11C-labeled choline analog pyrrolidinocholine into tissue was measured in the brain of three dogs by positron emission tomography (PET). During the first 90 s after the intravenous bolus injection of the tracer, transfer of tracer from plasma to tissue was unidirectional. The influx constant for pyrrolidinocholine into intracranial tissue, Kin, was 0.017 ml/g/min (0.008 SD), and the initial volume of distribution, V0, was 0.08 ml/g (0.03 SD). The influx constant was at least five times larger than the value expected if simple diffusion were to account for tissue uptake. The method presented in this paper can be used to investigate the availability of plasma choline and its analogs to the living human brain and other tissue in degenerative diseases affecting the cholinergic system, and to provide in vivo information on a choline transport system.",
author = "C Redies and M Diksic and B Collier and A Gjedde and Thompson, {C J} and S Gauthier and Feindel, {W H}",
year = "1988",
doi = "10.1002/syn.890020407",
language = "English",
volume = "2",
pages = "406--11",
journal = "Synapse",
issn = "0887-4476",
publisher = "Wiley",
number = "4",

}

RIS

TY - JOUR

T1 - Influx of a choline analog to dog brain measured by positron emission tomography.

AU - Redies, C

AU - Diksic, M

AU - Collier, B

AU - Gjedde, A

AU - Thompson, C J

AU - Gauthier, S

AU - Feindel, W H

PY - 1988

Y1 - 1988

N2 - The influx of the 11C-labeled choline analog pyrrolidinocholine into tissue was measured in the brain of three dogs by positron emission tomography (PET). During the first 90 s after the intravenous bolus injection of the tracer, transfer of tracer from plasma to tissue was unidirectional. The influx constant for pyrrolidinocholine into intracranial tissue, Kin, was 0.017 ml/g/min (0.008 SD), and the initial volume of distribution, V0, was 0.08 ml/g (0.03 SD). The influx constant was at least five times larger than the value expected if simple diffusion were to account for tissue uptake. The method presented in this paper can be used to investigate the availability of plasma choline and its analogs to the living human brain and other tissue in degenerative diseases affecting the cholinergic system, and to provide in vivo information on a choline transport system.

AB - The influx of the 11C-labeled choline analog pyrrolidinocholine into tissue was measured in the brain of three dogs by positron emission tomography (PET). During the first 90 s after the intravenous bolus injection of the tracer, transfer of tracer from plasma to tissue was unidirectional. The influx constant for pyrrolidinocholine into intracranial tissue, Kin, was 0.017 ml/g/min (0.008 SD), and the initial volume of distribution, V0, was 0.08 ml/g (0.03 SD). The influx constant was at least five times larger than the value expected if simple diffusion were to account for tissue uptake. The method presented in this paper can be used to investigate the availability of plasma choline and its analogs to the living human brain and other tissue in degenerative diseases affecting the cholinergic system, and to provide in vivo information on a choline transport system.

U2 - 10.1002/syn.890020407

DO - 10.1002/syn.890020407

M3 - Journal article

C2 - 3263708

VL - 2

SP - 406

EP - 411

JO - Synapse

JF - Synapse

SN - 0887-4476

IS - 4

ER -

ID: 14945441