Literature DB >> 30030127

Recovery from behavior and developmental effects of chronic oral methylphenidate following an abstinence period.

Connor Martin1, Dennis Fricke1, Abisha Vijayashanthar1, Courtney Lowinger1, Dimitris Koutsomitis1, Daniel Popoola1, Michael Hadjiargyrou2, David E Komatsu3, Panayotis K Thanos4.   

Abstract

Chronic oral methylphenidate (MP) exposure in rats is associated with numerous developmental and behavioral consequences. The present study investigated the persistence of the effects of chronic oral MP exposure after abstinence from MP use. Male and female rats were exposed to daily orally self-administered water, low dose MP (LD), or high dose (HD) MP for 13 weeks, followed by a 4-week abstinence period. Fluid, food consumption and bodyweights were monitored and animals were tested for locomotor activity, anxiety- and depressive-like symptoms, learning and memory, and social behavior during both the treatment and abstinence phases of the experiment. During treatment, MP attenuated bodyweight regardless of sex, but increased food and fluid consumption in females and males by 20.7% and 30.1%, respectively. MP also increased locomotor activity in both males and females observed as increased distance travelled in an open field. (59.1% and 95.9%, respectively) and increased locomotor activity in the home cage over a 24-hour circadian cycle (45.5% and 63.0%). Additionally, MP exerted an anxiolytic effect observed as increased time spent in the open arms of an elevated plus maze (31.1% in HD males, 59.2% in HD females), and an increased latency to immobility in a forced swim test (330% in HD males, 418% in HD females). The effects of MP (bodyweight, consumption, locomotion, anxiolytic, and anti-depressive) were, almost without exception, eliminated during the abstinence period. MP had no impact on learning and memory performance as measured by a T-maze, or social behavior during treatment. These findings suggest that the behavioral consequences of chronic oral MP treatment in our preclinical model are reversible in rats following an abstinence period from use of the drug.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Anxiety; Attention Deficit Hyperactivity Disorder; Methylphenidate; Psychostimulant; Ritalin; Sensitization

Mesh:

Substances:

Year:  2018        PMID: 30030127      PMCID: PMC6319957          DOI: 10.1016/j.pbb.2018.07.001

Source DB:  PubMed          Journal:  Pharmacol Biochem Behav        ISSN: 0091-3057            Impact factor:   3.533


  56 in total

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4.  Chronic oral methylphenidate treatment reversibly increases striatal dopamine transporter and dopamine type 1 receptor binding in rats.

Authors:  Lisa S Robison; Mala Ananth; Michael Hadjiargyrou; David E Komatsu; Panayotis K Thanos
Journal:  J Neural Transm (Vienna)       Date:  2017-01-23       Impact factor: 3.575

5.  Methylphenidate treatment during pre- and periadolescence alters behavioral responses to emotional stimuli at adulthood.

Authors:  Carlos A Bolaños; Michel Barrot; Olivier Berton; Deanna Wallace-Black; Eric J Nestler
Journal:  Biol Psychiatry       Date:  2003-12-15       Impact factor: 13.382

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Authors:  Claudio Lorello; Gary S Goldfield; Eric Doucet
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7.  Methylphenidate disrupts social play behavior in adolescent rats.

Authors:  Louk J M J Vanderschuren; Viviana Trezza; Sanne Griffioen-Roose; Olga J G Schiepers; Natascha Van Leeuwen; Taco J De Vries; Anton N M Schoffelmeer
Journal:  Neuropsychopharmacology       Date:  2008-02-27       Impact factor: 7.853

8.  Methylphenidate improves prefrontal cortical cognitive function through alpha2 adrenoceptor and dopamine D1 receptor actions: Relevance to therapeutic effects in Attention Deficit Hyperactivity Disorder.

Authors:  Amy Ft Arnsten; Anne G Dudley
Journal:  Behav Brain Funct       Date:  2005-04-22       Impact factor: 3.759

9.  Methylphenidate regulation of osteoclasts in a dose- and sex-dependent manner adversely affects skeletal mechanical integrity.

Authors:  Sardar M Z Uddin; Lisa S Robison; Dennis Fricke; Evan Chernoff; Michael Hadjiargyrou; Panayotis K Thanos; David E Komatsu
Journal:  Sci Rep       Date:  2018-01-24       Impact factor: 4.379

10.  Social Isolation Stress Induces Anxious-Depressive-Like Behavior and Alterations of Neuroplasticity-Related Genes in Adult Male Mice.

Authors:  Alessandro Ieraci; Alessandra Mallei; Maurizio Popoli
Journal:  Neural Plast       Date:  2016-01-06       Impact factor: 3.599

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  3 in total

1.  Brief and extended abstinence from chronic oral methylphenidate treatment produces reversible behavioral and physiological effects.

Authors:  Leanna Kalinowski; Carly Connor; Rathini Somanesan; Emily Carias; Kaleigh Richer; Lauren Smith; Connor Martin; Macauley Mackintosh; Daniel Popoola; Michael Hadjiargyrou; David E Komatsu; Panayotis K Thanos
Journal:  Dev Psychobiol       Date:  2019-08-27       Impact factor: 3.038

2.  Weekday-only chronic oral methylphenidate self-administration in male rats: Reversibility of the behavioral and physiological effects.

Authors:  Emily Carias; Dennis Fricke; Abisha Vijayashanthar; Lauren Smith; Rathini Somanesan; Connor Martin; Leanna Kalinowski; Daniel Popoola; Michael Hadjiargyrou; David E Komatsu; Panayotis K Thanos
Journal:  Behav Brain Res       Date:  2018-08-24       Impact factor: 3.332

3.  Fluoxetine Potentiates Oral Methylphenidate-Induced Gene Regulation in the Rat Striatum.

Authors:  Connor Moon; Matt Marion; Panayotis K Thanos; Heinz Steiner
Journal:  Mol Neurobiol       Date:  2021-07-02       Impact factor: 5.682

  3 in total

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