| Literature DB >> 26909848 |
Chelsea A Vadnie1, Jennifer Ayers-Ringler1, Alfredo Oliveros2, Osama A Abulseoud3, Sun Choi2, Mario J Hitschfeld3, Doo-Sup Choi4.
Abstract
Although neurotensin (NT) analogs are known to produce antipsychotic-like effects, the therapeutic possibility of a brain penetrant NTS1 agonist in treating psychiatric disorders has not been well studied. Here, we examined whether PD149163, a brain-penetrant NTS1-specific agonist, displays antipsychotic-like effects in C57BL/6J mice by investigating the effect of PD149163 on amphetamine-mediated hyperactivity and amphetamine-induced disruption of prepulse inhibition. In addition, we assessed the effect of PD149163 on glycogen synthase kinase-3 (GSK-3) activity, a downstream molecular target of antipsychotics and mood stabilizers, using phospho-specific antibodies. PD149163 (0.1 and 0.5mg/kg) inhibited amphetamine-induced hyperactivity in mice, indicating that NTS1 activation inhibits psychomotor agitation. PD149163 (0.5mg/kg) also increased prepulse inhibition, suggesting that NTS1 activation reduces prepulse inhibition deficits which often co-occur with psychosis in humans. Interestingly, PD149163 increased the inhibitory serine phosphorylation on both GSK-3α and GSK-3β in a dose- and time-dependent manner in the nucleus accumbens and medial prefrontal cortex of the mice. Moreover, PD149163 inhibited GSK-3 activity in the nucleus accumbens and medial prefrontal cortex in the presence of amphetamine. Thus, like most current antipsychotics and mood stabilizers, PD149163 inhibited GSK-3 activity in cortico-striatal circuitry. Together, our findings indicate that PD149163 may be a novel antipsychotic.Entities:
Keywords: Amphetamine; Glycogen synthase kinase 3; Locomotion; Neurotensin type 1 receptor; Prepulse inhibition
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Year: 2016 PMID: 26909848 PMCID: PMC4808331 DOI: 10.1016/j.bbr.2016.02.019
Source DB: PubMed Journal: Behav Brain Res ISSN: 0166-4328 Impact factor: 3.332