Reinforcing, subject-rated, and physiological effects of intranasal methylphenidate in humans: A dose-response analysis

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51 Citas (Scopus)

Resumen

The results of previously published reports suggest that oral methylphenidate has potential for abuse. An increase in insufflation of methylphenidate has been reported recently. To our knowledge, however, there are no published reports that examined the effects of intranasal methylphenidate. The purpose of this experiment was to characterize the reinforcing, subject-rated, and physiological effects of intranasal methylphenidate (0, 10, 20, and 30 mg). Eight volunteers (five males and three females) with recent histories of recreational stimulant use were recruited to participate in this experiment. Drug doses were administered in a double-blind fashion under medical supervision, but for safety purposes they were administered in ascending order. Intranasal methylphenidate increased the crossover point on the Multiple-Choice Questionnaire in a linear fashion, which suggests that intranasal methylphenidate functioned as a reinforcer. Intranasal methylphenidate also produced linear dose-dependent prototypical stimulant-like subjective effects (e.g. increases in ratings of Good Effects and High). Intranasal methylphenidate increased heart rate as a function of dose, but the magnitude of this effect was not clinically significant (i.e. average peak heart rate following administration of the highest dose was less than 82 beats per min). The results of this study suggest that across a range of doses, intranasal methylphenidate produces behavioral effects that are characteristic of abused stimulants. Future studies should test higher doses and directly compare the behavioral effects of intranasal methylphenidate to those of a prototypical abused stimulant (e.g. cocaine).

Idioma originalEnglish
Páginas (desde-hasta)179-186
Número de páginas8
PublicaciónDrug and Alcohol Dependence
Volumen71
N.º2
DOI
EstadoPublished - ago 20 2003

Nota bibliográfica

Funding Information:
This research was funded by the National Institute on Drug Abuse Grant DA 12665 (C.R.R.) and Grant M01 RR02602. W.W. Stoops is supported by NIDA Training Grant 5-T32-DA07304-03 awarded to the University of Kentucky Department of Behavioral Science.

Financiación

This research was funded by the National Institute on Drug Abuse Grant DA 12665 (C.R.R.) and Grant M01 RR02602. W.W. Stoops is supported by NIDA Training Grant 5-T32-DA07304-03 awarded to the University of Kentucky Department of Behavioral Science.

FinanciadoresNúmero del financiador
University of Kentucky Department of Behavioral Science
National Institute on Drug AbuseM01 RR02602, DA 12665
National Institute of Development Administration5-T32-DA07304-03

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Toxicology
    • Pharmacology
    • Psychiatry and Mental health
    • Pharmacology (medical)

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