Author/Authors :
John L. Musachio، نويسنده , , Jinsoo Hong، نويسنده , , Masanori Ichise، نويسنده , , Nicholas Seneca، نويسنده , , Amira K. Brown، نويسنده , , Jeih-San Liow، نويسنده , , Christer Halldin، نويسنده , , Robert B. Innis، نويسنده , , Victor W. Pike، نويسنده , , Rong He، نويسنده , , Wen-Jia Zhou، نويسنده , , Alan P. Kozikowski، نويسنده ,
Abstract :
11C-labeled (+)-trans-2-[[(3R,4S)-4-(4-chlorophenyl)-1-methylpiperidin-3-yl]methylsulfanyl]ethanol ([11C]5) and (+)-trans-2-[[(3R,4S)-4-(4-chlorophenyl)-1-methylpiperidin-3-yl]methylsulfanyl]-1-(piperidin-1-yl)ethanone ([11C]6) were synthesized and evaluated as new imaging agents for the norepinephrine transporter (NET). [11C]5 and [11C]6 display high affinity for the NET in vitro (Ki = 0.94 and 0.68 nM, respectively) and significant selectivity over the dopamine (DAT) and serotonin transporters (SERT). Because of their high affinity and favorable transporter selectivities we speculated that these ligands might serve as useful PET agents for imaging NET in vivo. Contrary to our expectations, both of these ligands provided brain images that were more typical of those shown by agents binding to the DAT.
Keywords :
PET imaging , DAT radioligands , Antidepression , NET radioligands , Brain imaging agents , Monoamine transporter inhibitors