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Psychopharmacology; Sep2005, Vol. 181 Issue 3, p537-549
Hou, R. H., Freeman, C., Langley, R. W., Szabadi, E., Bradshaw, C.
M.
Does modafinil activate the locus coeruleus in man? Comparison of modafinil
and clonidine on arousal and autonomic functions in human volunteers.
Rationale: Modafinil is a wakefulness-promoting drug
which is likely to activate some wakefulness-promoting and/or inhibit
sleep-promoting neurones in the brain. The locus coeruleus (LC) is a wakefulness-promoting
noradrenergic nucleus whose activity can be "switched off" by
the a2-adrenoceptor agonist clonidine, leading to sedative and sympatholytic
effects.
Objective: The aim of the study is to compare the effects
of single doses of modafinil and clonidine on arousal and autonomic functions
in human volunteers.
Methods: Sixteen healthy male volunteers participated
in four experimental sessions (modafinil 200 mg; clonidine 0.2 mg; modafinil
200 mg + clonidine 0.2 mg; placebo) at weekly intervals, according to
a balanced double-blind protocol. Arousal [pupillary "fatigue waves"
(PFW), critical flicker fusion frequency, self-ratings of alertness] and
autonomic functions (pupil diameter, pupillary light and darkness reflex
responses, blood pressure, heart rate, salivation) were recorded. Data
were analyzed with ANOVA, with multiple comparisons.
Results: Clonidine reduced subjective alertness, pupil
diameter, the initial velocity and amplitude of the darkness reflex response,
systolic and diastolic blood pressure and salivation, prolonged the recovery
time of the light reflex response and increased PFW. Modafinil reduced
PFW, increased pupil diameter and the initial velocity of the darkness
reflex response and tended to reduce the effect of clonidine on pupil
diameter and PFW. Modafinil had no effect on non-pupillary autonomic functions.
Conclusions: Clonidine exerted sympatholytic and sedative
effects, whereas modafinil had sympathomimetic and some alerting effects.
Modafinil may activate noradrenergic neurones in the LC involved in arousal
and pupillary control, without affecting extracoerulear noradrenergic
neurones involved in cardiovascular and salivary regulation.
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