Modafinil, a wake-promoting drug used to treat narcolepsy, is increasingly being used
as a cognitive enhancer. Although initially launched as distinct from stimulants that
increase extracellular dopamine by targeting dopamine transporters, recent preclinical
studies suggest otherwise.
To measure the acute effects of modafinil at doses used therapeutically (200 mg and
400 mg given orally) on extracellular dopamine and on dopamine transporters in the
male human brain.
Positron emission tomography with [(11)C]raclopride (D(2)/D(3) radioligand sensitive
to changes in endogenous dopamine) and [(11)C]cocaine (dopamine transporter radioligand)
was used to measure the effects of modafinil on extracellular dopamine and on dopamine
transporters in 10 healthy male participants. The study took place over an 8-month
period (2007-2008) at Brookhaven National Laboratory.
Primary outcomes were changes in dopamine D(2)/D(3) receptor and dopamine transporter
availability (measured by changes in binding potential) after modafinil when compared
with after placebo.
Modafinil decreased mean (SD) [(11)C]raclopride binding potential in caudate (6.1%
[6.5%]; 95% confidence interval [CI], 1.5% to 10.8%; P = .02), putamen (6.7% [4.9%];
95% CI, 3.2% to 10.3%; P = .002), and nucleus accumbens (19.4% [20%]; 95% CI, 5% to
35%; P = .02), reflecting increases in extracellular dopamine. Modafinil also decreased
[(11)C]cocaine binding potential in caudate (53.8% [13.8%]; 95% CI, 43.9% to 63.6%;
P < .001), putamen (47.2% [11.4%]; 95% CI, 39.1% to 55.4%; P < .001), and nucleus
accumbens (39.3% [10%]; 95% CI, 30% to 49%; P = .001), reflecting occupancy of dopamine
transporters.
In this pilot study, modafinil blocked dopamine transporters and increased dopamine
in the human brain (including the nucleus accumbens). Because drugs that increase
dopamine in the nucleus accumbens have the potential for abuse, and considering the
increasing use of modafinil, these results highlight the need for heightened awareness
for potential abuse of and dependence on modafinil in vulnerable populations.