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Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on August 8, 2008; DOI: 10.1124/jpet.108.143610


0022-3565/08/3272-573-583$20.00
JPET 327:573-583, 2008
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NEUROPHARMACOLOGY

Antidepressant-Like Pharmacological Profile of a Novel Triple Reuptake Inhibitor, (1S,2S)-3-(Methylamino)-2-(naphthalen-2-yl)-1-phenylpropan-1-ol (PRC200-SS)

Yanqi Liang, Amanda M. Shaw, Mona Boules, Siobhan Briody, Jessica Robinson, Alfredo Oliveros, Eric Blazar, Katrina Williams, Yiqun Zhang, Paul R. Carlier, and Elliott Richelson

Neuropsychopharmacology Laboratory, Mayo Foundation for Medical Education and Research and Mayo Clinic, Jacksonville, Florida (Y.L., A.M.S., M.B., S.B., J.R., A.O., E.B., K.W., E.R.); and Virginia Polytechnic Institute and State University, Department of Chemistry, Blacksburg, Virginia (Y.Z., P.R.C.)

Due to the putative involvement of dopaminergic circuits in depression, triple reuptake inhibitors are being developed as a new class of antidepressant, which is hypothesized to produce a more rapid onset and better efficacy than current antidepressants selective for serotonin or norepinephrine neurotransmission. (1S,2S)-3-(Methylamino)-2-(naphthalen-2-yl)-1-phenylpropan-1-ol (PRC200-SS), a new triple reuptake inhibitor, potently bound to the human serotonin, norepinephrine, and dopamine transporters with Kd values of 2.3, 0.63, and 18 nM, respectively. Inhibition of serotonin, norepinephrine, and dopamine uptake by PRC200-SS was also shown in cells expressing the corresponding transporter (Ki values of 2.1, 1.5, and 61 nM, respectively). In vivo, PRC200-SS dose-dependently decreased immobility in the forced-swim test in rats and in the tail-suspension test in mice, models predictive of antidepressant activity, with effects comparable with imipramine. These results in the behavioral models did not seem to result from the stimulation of locomotor activity. Consistent with the in vitro data and behavioral effects, peripheral administration of PRC200-SS (5 and 10 mg/kg i.p.) significantly increased extracellular levels of serotonin and norepinephrine in the medial prefrontal cortex, and of serotonin and dopamine in the core of nucleus accumbens, with reduction of levels of 3,4-dihydroxyphenylacetic acid, homovanillic acid, and 5-hydroxyindoleacetic acid compared with levels for saline control. Furthermore, PRC200-SS self-administration, which was used as a marker of abuse liability, was not observed with rats. Therefore, it seems that PRC200-SS may represent a novel triple reuptake inhibitor and possess antidepressant activity.


Received for publication July 16, 2008
Accepted August 7, 2008.

Address correspondence to: Dr. Yanqi Liang, Mayo Clinic, 4500 San Pablo Rd., Jacksonville, FL 32224. E-mail: liang.yanqi{at}mayo.edu







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