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Lack of deleterious effects of buspirone on cognition in healthy male volunteers

Lack of deleterious effects of buspirone on cognition in healthy male volunteers
Lack of deleterious effects of buspirone on cognition in healthy male volunteers

Buspirone is a serotonin 5-HT1A receptor agonist licensed for the treatment of anxiety. Other anxiolytic drugs such as benzodiazepines show significant sedative and other unwanted effects on cognition. Studies to date have yet to investigate cognitive effects of buspirone using well-validated computerized tests. The aim of this study was to assess acute subjective and cognitive effects of buspirone in healthy volunteers. Sixty healthy male volunteers received 20mg buspirone, 30mg buspirone, or placebo per os in a double-blind parallel groups design (N=20 per group). Subjective ratings (visual analogue scales) were completed at baseline, and at 1.5 and 3.5 hours post-capsule. Cognitive assessment was undertaken between 1.5 and 3.5 hours post-capsule, including tests of memory, executive planning, impulse control, decision making and cognitive flexibility. The 30mg buspirone group showed significantly higher subjective ratings of contentedness 3.5 hours after capsule relative to placebo. Treatment and placebo groups did not differ significantly on cognitive measures. In contrast to benzodiazepines, the anxiolytic buspirone appears to lack detectable deleterious effects on cognition when administered acutely at clinically meaningful doses. Future research directions are discussed in relation to acute and chronic studies in neuropsychiatric populations.

5-HT, Anxiety, Attention, Buspirone, Cognition, Depression, Serotonin
0269-8811
210-215
Chamberlain, Samuel R.
8a0e09e6-f51f-4039-9287-88debe8d8b6f
Müller, Ulrich
5389a6d4-a28e-4d4b-929f-c9542af406bd
Deakin, Julia B.
fa25fa25-ba03-407b-bb4b-afe8682932c8
Corlett, Phil R.
8562a855-4c02-4bf1-87dc-d963613af101
Dowson, Jonathan
d8866032-2456-46de-baa0-cc248e131e56
Cardinal, Rudolf N.
1fe91ac7-8f89-4064-90a3-26dc097ba229
Aitken, Michael R.F.
e1133575-00fd-46a6-ab76-e9fc7a1f5e6d
Robbins, Trevor W.
20dd57dd-dbf3-4aaa-b7ba-bb4387ffcbc7
Sahakian, Barbara J.
e689cd5c-b84f-4503-86ca-7526cf340121
Chamberlain, Samuel R.
8a0e09e6-f51f-4039-9287-88debe8d8b6f
Müller, Ulrich
5389a6d4-a28e-4d4b-929f-c9542af406bd
Deakin, Julia B.
fa25fa25-ba03-407b-bb4b-afe8682932c8
Corlett, Phil R.
8562a855-4c02-4bf1-87dc-d963613af101
Dowson, Jonathan
d8866032-2456-46de-baa0-cc248e131e56
Cardinal, Rudolf N.
1fe91ac7-8f89-4064-90a3-26dc097ba229
Aitken, Michael R.F.
e1133575-00fd-46a6-ab76-e9fc7a1f5e6d
Robbins, Trevor W.
20dd57dd-dbf3-4aaa-b7ba-bb4387ffcbc7
Sahakian, Barbara J.
e689cd5c-b84f-4503-86ca-7526cf340121

Chamberlain, Samuel R., Müller, Ulrich, Deakin, Julia B., Corlett, Phil R., Dowson, Jonathan, Cardinal, Rudolf N., Aitken, Michael R.F., Robbins, Trevor W. and Sahakian, Barbara J. (2007) Lack of deleterious effects of buspirone on cognition in healthy male volunteers. Journal of Psychopharmacology, 21 (2), 210-215. (doi:10.1177/0269881107068066).

Record type: Article

Abstract

Buspirone is a serotonin 5-HT1A receptor agonist licensed for the treatment of anxiety. Other anxiolytic drugs such as benzodiazepines show significant sedative and other unwanted effects on cognition. Studies to date have yet to investigate cognitive effects of buspirone using well-validated computerized tests. The aim of this study was to assess acute subjective and cognitive effects of buspirone in healthy volunteers. Sixty healthy male volunteers received 20mg buspirone, 30mg buspirone, or placebo per os in a double-blind parallel groups design (N=20 per group). Subjective ratings (visual analogue scales) were completed at baseline, and at 1.5 and 3.5 hours post-capsule. Cognitive assessment was undertaken between 1.5 and 3.5 hours post-capsule, including tests of memory, executive planning, impulse control, decision making and cognitive flexibility. The 30mg buspirone group showed significantly higher subjective ratings of contentedness 3.5 hours after capsule relative to placebo. Treatment and placebo groups did not differ significantly on cognitive measures. In contrast to benzodiazepines, the anxiolytic buspirone appears to lack detectable deleterious effects on cognition when administered acutely at clinically meaningful doses. Future research directions are discussed in relation to acute and chronic studies in neuropsychiatric populations.

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More information

Published date: March 2007
Keywords: 5-HT, Anxiety, Attention, Buspirone, Cognition, Depression, Serotonin

Identifiers

Local EPrints ID: 493103
URI: http://eprints.soton.ac.uk/id/eprint/493103
ISSN: 0269-8811
PURE UUID: db1afe47-d31c-423a-bece-005130fe3083
ORCID for Samuel R. Chamberlain: ORCID iD orcid.org/0000-0001-7014-8121

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Date deposited: 22 Aug 2024 17:21
Last modified: 23 Aug 2024 01:59

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Contributors

Author: Samuel R. Chamberlain ORCID iD
Author: Ulrich Müller
Author: Julia B. Deakin
Author: Phil R. Corlett
Author: Jonathan Dowson
Author: Rudolf N. Cardinal
Author: Michael R.F. Aitken
Author: Trevor W. Robbins
Author: Barbara J. Sahakian

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