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AbstractAbstract
[en] Iodovesamicol analogs, radioiodinated at the ortho (1), meta(2) and para(3) positions of the 4-phenylpiperidine moiety, were evaluated as potential presynaptic cholinergic neuron mapping agents. Significant accumulation of m-[125I]iodovesamicol (mIV(2)) (about 3% of the injected dose) was noted in the rat brain with prolonged retention times. The accumulation of mIV(2) in the rat brain was decreased by 67% by 5 min pre-injection of dl-vesamicol(1 μmol/kg). Pre-injection of (+)-3-(3-hydroxyphenyl)-N-(1-propyl)piperdine[(+)-3-PPP](0.75 μmol/kg) did not markedly decrease the levels of radiotracers (oIV(1) and mIV(2)) in the rat brain. These results suggest that radioiodinated m-iodovesamicol (mIV(2)) is suitable for use in presynaptic cholinergic neuron mapping
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Copyright (c) 1995 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
Record Type
Journal Article
Journal
Country of publication
AMINES, ANIMAL CELLS, ANIMALS, AZINES, BETA DECAY RADIOISOTOPES, BODY, CENTRAL NERVOUS SYSTEM, CHEMICAL REACTIONS, DAYS LIVING RADIOISOTOPES, ELECTRON CAPTURE RADIOISOTOPES, HALOGENATION, HETEROCYCLIC COMPOUNDS, INTERMEDIATE MASS NUCLEI, INTERNAL CONVERSION RADIOISOTOPES, IODINE ISOTOPES, ISOTOPES, MAMMALS, NERVOUS SYSTEM, NUCLEI, ODD-EVEN NUCLEI, ORGANIC COMPOUNDS, ORGANIC NITROGEN COMPOUNDS, ORGANS, PYRIDINES, RADIOISOTOPES, RODENTS, SOMATIC CELLS, VERTEBRATES
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