Comparison of pramipexole and amisulpride on alertness, autonomic and endocrine functions in healthy volunteers
Comparison of pramipexole and amisulpride on alertness, autonomic and endocrine functions in healthy volunteers
Rationale In a previous study in healthy volunteers, the anti-Parkinsonian drug pramipexole caused sedation and pupil dilatation, consistent with the stimulation of inhibitory D2/D3 autoreceptors on the ventral tegmental area dopaminergic neurones. The sedation may be related to the removal of the dopaminergic excitation of the locus coeruleus (via the meso-coerulear pathway), whereas the pupil dilatation may be due to the removal of the dopaminergic excitation of the Edinger–Westphal nucleus (via a putative meso-pupillomotor pathway).
Objectives We investigated the hypothesis that amisulpride, a D2/D3 receptor antagonist, would have effects opposite to those of pramipexole on alertness, pupillary and endocrine functions.
Materials and methods Pramipexole (0.5 mg), amisulpride (50 mg), and their combination were administered to 16 healthy males in a balanced, cross-over, double-blind design. Tests included measures of alertness (Pupillographic Sleepiness Test, critical flicker fusion frequency, visual analogue scales), pupillary functions (resting pupil diameter, light and darkness reflex responses), non-pupillary autonomic functions (heart rate, blood pressure, salivation, core temperature), and endocrine functions [blood concentrations of prolactin, growth hormone (GH) and thyroid stimulating hormone (TSH)]. Data were analysed by ANOVA.
Results Pramipexole reduced alertness and pupillary light reflex response amplitude, tended to reduce core temperature, reduced prolactin levels and increased GH levels. Amisulpride reduced pupil diameter, increased the amplitude of the light reflex response and prolactin and TSH levels.
Conclusions The opposite effects of pramipexole and amisulpride on alertness, pupillary function and pituitary hormone levels are consistent with their interactions with inhibitory D2/D3 receptors on VTA neurones and in the tuberoinfundibular system.
pramipexole, amisulpride, alertness, pupil diameter, locus coeruleus, Edinger–Westphal
nucleus . Ventral tegmental area
498-510
Samuels, E.R.
be1fd344-e73a-43da-aca8-33c6e21cb7f2
Hou, R.H.
470bdcbc-93a9-4dad-aac5-26d455c34376
Langley, R.W.
579cc42e-972f-4422-952f-1c76ecc4b4e3
Szabadi, E.
cff688f8-264f-4ca3-a2c4-cb10930f1956
Bradshaw, C.M.
0baafd10-0e91-4113-b90b-27132bd77305
September 2006
Samuels, E.R.
be1fd344-e73a-43da-aca8-33c6e21cb7f2
Hou, R.H.
470bdcbc-93a9-4dad-aac5-26d455c34376
Langley, R.W.
579cc42e-972f-4422-952f-1c76ecc4b4e3
Szabadi, E.
cff688f8-264f-4ca3-a2c4-cb10930f1956
Bradshaw, C.M.
0baafd10-0e91-4113-b90b-27132bd77305
Samuels, E.R., Hou, R.H., Langley, R.W., Szabadi, E. and Bradshaw, C.M.
(2006)
Comparison of pramipexole and amisulpride on alertness, autonomic and endocrine functions in healthy volunteers.
Psychopharmacology, 187 (4), .
(doi:10.1007/s00213-006-0443-y).
(PMID:16802163)
Abstract
Rationale In a previous study in healthy volunteers, the anti-Parkinsonian drug pramipexole caused sedation and pupil dilatation, consistent with the stimulation of inhibitory D2/D3 autoreceptors on the ventral tegmental area dopaminergic neurones. The sedation may be related to the removal of the dopaminergic excitation of the locus coeruleus (via the meso-coerulear pathway), whereas the pupil dilatation may be due to the removal of the dopaminergic excitation of the Edinger–Westphal nucleus (via a putative meso-pupillomotor pathway).
Objectives We investigated the hypothesis that amisulpride, a D2/D3 receptor antagonist, would have effects opposite to those of pramipexole on alertness, pupillary and endocrine functions.
Materials and methods Pramipexole (0.5 mg), amisulpride (50 mg), and their combination were administered to 16 healthy males in a balanced, cross-over, double-blind design. Tests included measures of alertness (Pupillographic Sleepiness Test, critical flicker fusion frequency, visual analogue scales), pupillary functions (resting pupil diameter, light and darkness reflex responses), non-pupillary autonomic functions (heart rate, blood pressure, salivation, core temperature), and endocrine functions [blood concentrations of prolactin, growth hormone (GH) and thyroid stimulating hormone (TSH)]. Data were analysed by ANOVA.
Results Pramipexole reduced alertness and pupillary light reflex response amplitude, tended to reduce core temperature, reduced prolactin levels and increased GH levels. Amisulpride reduced pupil diameter, increased the amplitude of the light reflex response and prolactin and TSH levels.
Conclusions The opposite effects of pramipexole and amisulpride on alertness, pupillary function and pituitary hormone levels are consistent with their interactions with inhibitory D2/D3 receptors on VTA neurones and in the tuberoinfundibular system.
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Published date: September 2006
Keywords:
pramipexole, amisulpride, alertness, pupil diameter, locus coeruleus, Edinger–Westphal
nucleus . Ventral tegmental area
Organisations:
Community Clinical Sciences, Infection Inflammation & Immunity, Clinical Neurosciences
Identifiers
Local EPrints ID: 181859
URI: http://eprints.soton.ac.uk/id/eprint/181859
ISSN: 0033-3158
PURE UUID: 534f3365-cad5-43ed-b8ab-be85235e6b59
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Date deposited: 04 May 2011 13:28
Last modified: 15 Mar 2024 03:28
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Contributors
Author:
E.R. Samuels
Author:
R.W. Langley
Author:
E. Szabadi
Author:
C.M. Bradshaw
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