Correction to In Vivo Imaging of Human Neuroinflammation
Author(s) -
Daniel Albrecht,
Cristina Granziera,
Jacob M. Hooker,
Marco L. Loggia
Publication year - 2018
Publication title -
acs chemical neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.158
H-Index - 69
ISSN - 1948-7193
DOI - 10.1021/acschemneuro.8b00188
Subject(s) - neuroinflammation , neuroscience , in vivo , neuroimaging , computational biology , psychology , medicine , pharmacology , computer science , biology , inflammation , microbiology and biotechnology
We recently noticed a typo in our 2016 article, “In Vivo Imaging of Human Neuroinflammation” published in ACS Chemical Neuroscience. In the original version, the language on page 474 reads: Selective MAO-B antagonists have been radiolabeled for PET imaging of astrocytes, including [C]-D-deprenyl and its deuterium substituted analogue, [C]-deprenyl-D2. [C]deprenyl-D2 is the most commonly used astrocyte tracer, because of its favorable kinetics compared to [C]deprenyl. However, specific binding of the molecule has been questioned. The first “[C]-D-deprenyl” should have been “[C]-Ldeprenyl”. We also add a statement about [C]-D-deprenyl. The corrected language is as follows: Selective MAO-B antagonists have been radiolabeled for PET imaging of astrocytes, including [C]-L-deprenyl and its deuterium substituted analogue, [C]-L-deprenyl-D2. [C]-L-deprenyl-D2 is the most commonly used astrocyte tracer, because of its favorable kinetics compared to [C]-Ldeprenyl. The mirror enantiomer of L-deprenyl, D-deprenyl, has also been radiolabeled for use as an astrocytic marker. However, reduced affinity for MAO-B and questionable specific binding of the molecule limit the practicality of using Ddeprenyl as an astrocytic marker. Correction
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