The discriminative stimulus properties of methylphenidate in C57BL/6J mice
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作者:
McGovern, Robin W.
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Med Univ S Carolina, Ctr Drug & Alcohol Programs, Charleston, SC 29425 USA
Med Univ S Carolina, Dept Pharmaceut & Biomed Sci, Charleston, SC 29425 USAMed Univ S Carolina, Ctr Drug & Alcohol Programs, Charleston, SC 29425 USA
McGovern, Robin W.
[1
,4
]
Middaugh, Lawrence D.
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Med Univ S Carolina, Ctr Drug & Alcohol Programs, Charleston, SC 29425 USA
Med Univ S Carolina, Dept Neurosci, Charleston, SC 29425 USAMed Univ S Carolina, Ctr Drug & Alcohol Programs, Charleston, SC 29425 USA
Middaugh, Lawrence D.
[1
,3
]
Patrick, Kennerly S.
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Med Univ S Carolina, Dept Pharmaceut & Biomed Sci, Charleston, SC 29425 USAMed Univ S Carolina, Ctr Drug & Alcohol Programs, Charleston, SC 29425 USA
Patrick, Kennerly S.
[4
]
Griffin, William C., III
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Med Univ S Carolina, Ctr Drug & Alcohol Programs, Charleston, SC 29425 USA
Med Univ S Carolina, Dept Psychiat & Behav Sci, Charleston, SC 29425 USAMed Univ S Carolina, Ctr Drug & Alcohol Programs, Charleston, SC 29425 USA
Griffin, William C., III
[1
,2
]
机构:
[1] Med Univ S Carolina, Ctr Drug & Alcohol Programs, Charleston, SC 29425 USA
[2] Med Univ S Carolina, Dept Psychiat & Behav Sci, Charleston, SC 29425 USA
[3] Med Univ S Carolina, Dept Neurosci, Charleston, SC 29425 USA
[4] Med Univ S Carolina, Dept Pharmaceut & Biomed Sci, Charleston, SC 29425 USA
Methylphenidate (MPH) therapy for attention-deficit/hyperactivity disorder is common in children and adults. Concerns regarding abuse of MPH prompted studies to better understand its pharmacology. We used an established drug discrimination task to determine whether MPH could be discriminated by C57BL/6J (B6) mice. B6 mice learned to discriminate cues produced by racemic MPH (dl-MPH 5.0 mg/kg) or half the dose of pure d-isomer (2.5 mg/kg), and dose-response tests established appropriate reductions in discrimination with declining dose. Importantly, the two drug forms generalized to each other completely in substitution tests; consistent with reports that the l-isomer is pharmacodynamically inactive. An additional experiment indicated that lower doses (1 and 2 mg/kg) of dl-MPH did not support acquisition of MPH discrimination despite extensive training. Mice acquired discrimination of dl-MPH only when the dose was increased to 4 mg/kg. Thus, although these lower doses increased drug lever responding in mice trained on the higher dose, their stimuli were not sufficient to support acquisition of the discrimination task. These findings correspond to earlier studies conducted in our laboratory on threshold doses needed to produce stimulatory effects of motor activity in B6 mice. These preclinical findings provide insight into the relative potency, and by extension, efficacy of dl-MPH versus d-MPH doses. Behavioural Pharmacology 22: 14-22 (C) 2011 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.