Effects of COMT genotype and tolcapone on lapses of sustained attention after sleep deprivation in healthy young men
Autor: | Michael Sommerauer, Christian R. Baumann, Sebastian C. Holst, Alessandro Borrello, Susanne Weigend, Wolfgang Berger, Thomas Müller, Hans-Peter Landolt, Amandine Valomon |
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Přispěvatelé: | University of Zurich, Landolt, Hans-Peter |
Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Male medicine.medical_specialty Genotype 10050 Institute of Pharmacology and Toxicology 610 Medicine & health Placebo Catechol O-Methyltransferase Polymorphism Single Nucleotide Article 03 medical and health sciences 11124 Institute of Medical Molecular Genetics 2738 Psychiatry and Mental Health Young Adult 0302 clinical medicine Dopamine Internal medicine medicine Humans Attention Prefrontal cortex Pharmacology Tolcapone business.industry Dopaminergic Catechol O-Methyltransferase Inhibitors Sleep in non-human animals 10040 Clinic for Neurology Sleep deprivation Psychiatry and Mental health 030104 developmental biology Endocrinology 3004 Pharmacology 10076 Center for Integrative Human Physiology 570 Life sciences biology Sleep Deprivation Wakefulness medicine.symptom business 030217 neurology & neurosurgery medicine.drug |
Zdroj: | Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. 43(7) |
ISSN: | 1740-634X |
Popis: | Tolcapone, a brain penetrant selective inhibitor of catechol-O-methyltransferase (COMT) devoid of psychostimulant properties, improves cognition and cortical information processing in rested volunteers, depending on the genotype of the functional Val158Met polymorphism of COMT. The impact of this common genetic variant on behavioral and neurophysiological markers of increased sleep need after sleep loss is controversial. Here we investigated the potential usefulness of tolcapone to mitigate consequences of sleep deprivation on lapses of sustained attention, and tested the hypothesis that dopamine signaling in the prefrontal cortex (PFC) causally contributes to neurobehavioral and neurophysiological markers of sleep homeostasis in humans. We first quantified in 73 young male volunteers the impact of COMT genotype on the evolution of attentional lapses during 40 h of extended wakefulness. Subsequently, we tested in an independent group of 30 young men whether selective inhibition of COMT activity with tolcapone counteracts attentional and neurophysiological markers of elevated sleep need in a genotype-dependent manner. Neither COMT genotype nor tolcapone affected brain electrical activity in wakefulness and sleep. By contrast, COMT genotype and tolcapone modulated the sleep loss-induced impairment of vigilant attention. More specifically, Val/Met heterozygotes produced twice as many lapses after a night without sleep than Met/Met homozygotes. Unexpectedly, tolcapone further deteriorated the sleep loss-induced performance deficits when compared to placebo, particularly in Val/Met and Met/Met genotypes. The findings suggest that PFC dopaminergic tone regulates sustained attention after sleep loss according to an inverse U-shape relationship, independently of neurophysiological markers of elevated sleep need. |
Databáze: | OpenAIRE |
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