Entity

Time filter

Source Type


Carli M.,Laboratory Neurochemistry and Behavior | Kostoula C.,Laboratory Neurochemistry and Behavior | Sacchetti G.,Laboratory Neurochemistry and Behavior | Mainolfi P.,Laboratory Neurochemistry and Behavior | And 3 more authors.
Journal of Neurochemistry | Year: 2015

Variants of tryptophan hydroxylase-2 (Tph2), the gene encoding enzyme responsible for the synthesis of brain serotonin (5-HT), have been associated with neuropsychiatric disorders, substance abuse and addiction. This study assessed the effect of Tph2 gene deletion on motor behavior and found that motor activity induced by 2.5 and 5 mg/kg amphetamine was enhanced in Tph2-/- mice. Using the in vivo microdialysis technique we found that the ability of amphetamine to stimulate noradrenaline (NA) release in the striatum was reduced by about 50% in Tph2-/- mice while the release of dopamine (DA) was not affected. Tph2 deletion did not affect the release of NA and DA in the prefrontal cortex. The role of endogenous 5-HT in enhancing the effect of amphetamine was confirmed showing that treatment with the 5-HT precursor 5-hydroxytryptophan (10 mg/kg) restored tissue and extracellular levels of brain 5-HT and the effects of amphetamine on striatal NA release and motor activity in Tph2-/- mice. Treatment with the NA precursor dihydroxyphenylserine (400 mg/kg) was sufficient to restore the effect of amphetamine on striatal NA release and motor activity in Tph2-/- mice. These findings indicate that amphetamine-induced hyperactivity is attenuated by endogenous 5-HT through the inhibition of striatal NA release. Tph2-/- mice may be a useful preclinical model to assess the role of 5-HT-dependent mechanisms in the action of psychostimulants. © 2015 International Society for Neurochemistry. Source

Discover hidden collaborations