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Early Adolescence is a Critical Period for the Maturation of Inhibitory Behavior.

Author(s): Reynolds LM, Yetnikoff L, Pokinko M, Wodzinski M, Epelbaum JG, Lambert LC, Cossette MP, Arvanitogiannis A, Flores C

Cereb Cortex. 2018 Oct 06;: Authors: Reynolds LM, Yetnikoff L, Pokinko M, Wodzinski M, Epelbaum JG, Lambert LC, Cossette MP, Arvanitogiannis A, Flores C

Article GUID: 30295713

Differential sensitivity to the acute and sensitizing behavioral effects of methylphenidate as a function of strain in adolescent and young adult rats.

Author(s): Yetnikoff L, Arvanitogiannis A

Behav Brain Funct. 2013 Oct 17;9:38 Authors: Yetnikoff L, Arvanitogiannis A

Article GUID: 24134881

Endocannabinoids promote cocaine-induced impulsivity and its rapid dopaminergic correlates.

Author(s): Hernandez G, Oleson EB, Gentry RN, Abbas Z, Bernstein DL, Arvanitogiannis A, Cheer JF

Biol Psychiatry. 2014 Mar 15;75(6):487-98 Authors: Hernandez G, Oleson EB, Gentry RN, Abbas Z, Bernstein DL, Arvanitogiannis A, Cheer JF

Article GUID: 24138924

Dampened Mesolimbic Dopamine Function and Signaling by Saturated but not Monounsaturated Dietary Lipids.

Author(s): Hryhorczuk C, Florea M, Rodaros D, Poirier I, Daneault C, Des Rosiers C, Arvanitogiannis A, Alquier T, Fulton S

Neuropsychopharmacology. 2016 Feb;41(3):811-21 Authors: Hryhorczuk C, Florea M, Rodaros D, Poirier I, Daneault C, Des Rosiers C, Arvanitogiannis A, Alquier T, Fulton S

Article GUID: 26171719

Non-Contingent Exposure to Amphetamine in Adolescence Recruits miR-218 to Regulate Dcc Expression in the VTA.

Author(s): Cuesta S, Restrepo-Lozano JM, Silvestrin S, Nouel D, Torres-Berrío A, Reynolds LM, Arvanitogiannis A, Flores C

Neuropsychopharmacology. 2018 03;43(4):900-911 Authors: Cuesta S, Restrepo-Lozano JM, Silvestrin S, Nouel D, Torres-Berrío A, Reynolds LM, Arvanitogiannis A, Flores C

Article GUID: 29154364

Adolescent Exposure to Methylphenidate Increases Impulsive Choice Later in Life.

Author(s): Abbas Z, Sweet A, Hernandez G, Arvanitogiannis A

Front Behav Neurosci. 2017;11:214 Authors: Abbas Z, Sweet A, Hernandez G, Arvanitogiannis A

Article GUID: 29163086


Title:Adolescent Exposure to Methylphenidate Increases Impulsive Choice Later in Life.
Authors:Abbas ZSweet AHernandez GArvanitogiannis A
Link:https://www.ncbi.nlm.nih.gov/pubmed/29163086?dopt=Abstract
Category:Front Behav Neurosci
PMID:29163086
Dept Affiliation: CSBN
1 Department of Psychology, Center for Studies in Behavioral Neurobiology, Concordia University, Montreal, QC, Canada.
2 Groupe de Recherche sur le Système Nerveux Central, Faculté de Pharmacie, Université de Montréal, Montreal, QC, Canada.
3 Groupe de Recherche sur le Système Nerveux Central, Département de Pharmacologie et Physiologie, Université de Montréal, Montreal, QC, Canada.
4 Département de Neuroscience, Université de Montréal, Montreal, QC, Canada.

Description:

Adolescent Exposure to Methylphenidate Increases Impulsive Choice Later in Life.

Front Behav Neurosci. 2017;11:214

Authors: Abbas Z, Sweet A, Hernandez G, Arvanitogiannis A

Abstract

Background: The psychostimulant methylphenidate (MPH) is known to temporarily reduce impulsive choice and promote self-control. What is not sufficiently understood is how repeated treatment with MPH affects impulsive choice in the long run, and whether any such effect is contingent on exposure at certain developmental stages. Methods: Using an animal model for impulsive choice, we examined first whether giving MPH through early adolescence alters delay discounting, an operational measure of impulsive choice, later in adulthood. We then tested whether equivalent long-term effects are observed if exposure to the drug occurred during adulthood. Starting on postnatal day 25 or postnatal day 60, male rats received one of a range of doses of MPH for 10 consecutive days. Twenty-six days later, all rats were trained to choose between a lever that produced a small immediate reward and a lever that produced a large reward after a range of delays. Results: Rats showed a long-term decrease in the selection of the delayed larger reward when treated with moderate doses of MPH during early adolescence, but not when treated with the lower or higher doses. In contrast, no differences were observed in the selection of the delayed larger reward in animals that were treated with various doses of MPH during adulthood. Conclusions: Our findings suggest effects of MPH on impulsive choice that are contingent on dosage and on the developmental period of exposure. When administered during adolescence, moderate doses of MPH increase impulsive choice long after the end of treatment, whereas these same doses administered during adulthood were without effect.

PMID: 29163086 [PubMed]