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Exploration of Sulfur‐Containing Analogues for Imaging Vesicular Acetylcholine Transporter in the Brain
Author(s) -
Luo Zonghua,
Liu Hui,
Jin Hongjun,
Gu Jiwei,
Yu Yanbo,
Kaneshige Kota,
Perlmutter Joel S.,
Parsons Stanley M.,
Tu Zhude
Publication year - 2018
Publication title -
chemmedchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.817
H-Index - 100
eISSN - 1860-7187
pISSN - 1860-7179
DOI - 10.1002/cmdc.201800411
Subject(s) - vesicular acetylcholine transporter , chemistry , in vivo , ligand (biochemistry) , striatum , transporter , receptor , biodistribution , stereochemistry , ex vivo , pharmacology , biochemistry , in vitro , acetylcholine , endocrinology , biology , dopamine , microbiology and biotechnology , gene , choline acetyltransferase
Sixteen new sulfur‐containing compounds targeting the vesicular acetylcholine transporter (VAChT) were synthesized and assessed for in vitro binding affinities. Enantiomers (−)‐(1‐(3‐hydroxy‐1,2,3,4‐tetrahydronaphthalen‐2‐yl)piperidin‐4‐yl)(4‐(methylthio)phenyl)methanone [(−)‐ 8 ] and (−)‐(4‐((2‐fluoroethyl)thio)phenyl)(1‐(3‐hydroxy‐1,2,3,4‐tetrahydronaph‐thalen‐2‐yl)piperidin‐4‐yl)methanone [(−)‐ 14 a ] displayed high binding affinities, with respective K i values of 1.4 and 2.2 n m for human VAChT, moderate and high selectivity for human VAChT over σ 1 (≈13‐fold) and σ 2 receptors (>420‐fold). Radiosyntheses of (−)‐[ 11 C] 8 and (−)‐[ 18 F] 14 a were achieved using conventional methods. Ex vivo autoradiography and biodistribution studies in Sprague–Dawley rats indicated that both radiotracers have the capacity to penetrate the blood–brain barrier, with high initial brain uptake at 5 min and rapid washout. The striatal region had the highest accumulation for both radiotracers. Pretreating the rats with the VAChT ligand (−)‐vesamicol decreased brain uptake for both radiotracers. Pretreating the rats with the σ 1 ligand YUN‐122 ( N ‐(4‐benzylcyclohexyl)‐2‐(2‐fluorophenyl)acetamide) also decreased brain uptake, suggesting these two radiotracers also bind to the σ 1 receptor in vivo. The microPET study of (−)‐[ 11 C] 8 in the brain of a non‐human primate showed high striatal accumulation that peaked quickly and washed out rapidly. Although preliminary results indicated these two sulfur‐containing radiotracers have high binding affinities for VAChT with rapid washout kinetics from the striatum, their σ 1 receptor binding properties limit their potential as radiotracers for quantifying VAChT in vivo.