Abstract

Several lines of evidence indicate that the use of stimulant drugs, including methylphenidate (MPD), increases tobacco smoking. This has raised concerns that MPD use during adolescence could facilitate nicotine abuse. Preclinical studies have shown that repeated treatment with an addictive drug produces sensitization to that drug and usually cross-sensitization to other drugs. Behavioral sensitization has been implicated in the development of drug addiction. We examined whether repeated oral MPD administration during adolescence could induce behavioral sensitization to MPD and long-lasting cross-sensitization to nicotine. Adolescent male Wistar rats were treated orally with 10 mg/kg MPD or saline (SAL) from postnatal day (PND) 27 to 33. To evaluate behavioral sensitization to MPD in adolescent rats (PND 39), the SAL pretreated group was subdivided into two groups that received intragastric SAL (1.0 mL/kg) or MPD (10 mg/kg); MPD pretreated rats received MPD (10 mg/kg). Cross-sensitization was evaluated on PND 39 or PND 70 (adulthood). To this end, SAL- and MPD-pretreated groups received subcutaneous injections of SAL (1.0 mL/kg) or nicotine (0.4 mg/kg). All groups had 8 animals. Immediately after injections, locomotor activity was determined. The locomotor response to MPD challenge of MPD-pretreated rats was not significantly different from that of the SAL-pretreated group. Moreover, the locomotor response of MPD-pretreated rats to nicotine challenge was not significantly different from that of the SAL-pretreated group. This lack of sensitization and cross-sensitization suggests that MPD treatment during adolescence does not induce short- or long-term neuroadaptation in rats that could increase sensitivity to MPD or nicotine.

Highlights

  • Attention deficit hyperactivity disorder (ADHD) is the most commonly diagnosed and treated psychiatric disorder of childhood

  • Comparisons across groups indicated for both adolescent and adult rats that nicotine significantly increased locomotor activity in both saline- (SAL + NIC) and MPD- (MPD + NIC) pretreated groups compared to the control (SAL + SAL) group

  • Our data demonstrated that repeated treatment with intragastric MPD did not induce behavioral sensitization in adolescent rats

Read more

Summary

Introduction

Attention deficit hyperactivity disorder (ADHD) is the most commonly diagnosed and treated psychiatric disorder of childhood. The psychostimulant methylphenidate (MPD), commonly known as Ritalin®, is one of the most prescribed drugs for the treatment of ADHD. Children with ADHD are treated for several years, with drug administration often extending to adolescence and adulthood [1]. MPD promotes many of the neurochemical effects typically associated with other psychomotor stimulants, including increases in extracellular dopamine and norepinephrine [2]. These effects are mediated by MPD binding to the dopamine transporter and to the norepinephrine transporter, respectively, which blocks the neurotransmitters’ transport through the nerve terminals [2]. MPD may act on serotonin transporters [3]

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call