BACKGROUND: Methylphenidate has been suggested to exert its therapeutic effect mainly by blocking the dopamine transporter. In spite of the importance of this interaction, no detailed information is available yet on its actions on single dopaminergic neurons. METHODS: We examined the effects of methylphenidate on dopaminergic neurons using electrophysiological recordings from rat midbrain slices. RESULTS: Methylphenidate inhibited spontaneous firing and caused a membrane hyperpolarization in current clamp or an outward current in voltage clamp. These effects were antagonized by the D(2) receptor antagonist sulpiride. An acute dopamine-depleting treatment of the slices with the dopa-decarboxylase inhibitor carbidopa significantly reduced the effects of methylphenidate. This drug potentiated, in a concentration-dependent manner, cellular responses to exogenous dopamine application. CONCLUSIONS: Our electrophysiological data are consistent with the hypothesis that methylphenidate inhibits dopamine transporter and suggest that the depression of firing is mediated by the release of newly synthesized dopamine which accumulates extracellularly due to inhibition of its reuptake.
BACKGROUND:Methylphenidate has been suggested to exert its therapeutic effect mainly by blocking the dopamine transporter. In spite of the importance of this interaction, no detailed information is available yet on its actions on single dopaminergic neurons. METHODS: We examined the effects of methylphenidate on dopaminergic neurons using electrophysiological recordings from rat midbrain slices. RESULTS:Methylphenidate inhibited spontaneous firing and caused a membrane hyperpolarization in current clamp or an outward current in voltage clamp. These effects were antagonized by the D(2) receptor antagonist sulpiride. An acute dopamine-depleting treatment of the slices with the dopa-decarboxylase inhibitor carbidopa significantly reduced the effects of methylphenidate. This drug potentiated, in a concentration-dependent manner, cellular responses to exogenous dopamine application. CONCLUSIONS: Our electrophysiological data are consistent with the hypothesis that methylphenidate inhibits dopamine transporter and suggest that the depression of firing is mediated by the release of newly synthesized dopamine which accumulates extracellularly due to inhibition of its reuptake.
Authors: Felipe Schmitz; Paula Pierozan; André F Rodrigues; Helena Biasibetti; Matheus Grunevald; Letícia F Pettenuzzo; Giselli Scaini; Emilio L Streck; Carlos A Netto; Angela T S Wyse Journal: Mol Neurobiol Date: 2016-06-21 Impact factor: 5.590
Authors: Mauro Federici; Emanuele Claudio Latagliata; Ada Ledonne; Francesca R Rizzo; Marco Feligioni; Dave Sulzer; Matthew Dunn; Dalibor Sames; Howard Gu; Robert Nisticò; Stefano Puglisi-Allegra; Nicola B Mercuri Journal: J Biol Chem Date: 2013-11-26 Impact factor: 5.157
Authors: Johannes Buchmann; A Dueck; W Gierow; H Zamorski; S Heinicke; H Heinrich; J Hoeppner; T Klauer; O Reis; F Haessler Journal: J Neural Transm (Vienna) Date: 2009-12-10 Impact factor: 3.575
Authors: Belén Goitia; Mariana Raineri; Laura E González; José L Rozas; Edgar Garcia-Rill; Verónica Bisagno; Francisco J Urbano Journal: J Neurochem Date: 2013-01-07 Impact factor: 5.372