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Acute neuropharmacological effects of atomoxetine on inhibitory control in ADHD children: A fNIRS study

The object of the current study is to explore the neural substrate for effects of atomoxetine (ATX) on inhibitory control in school-aged children with attention deficit hyperactivity disorder (ADHD) using functional near-infrared spectroscopy (fNIRS). We monitored the oxy-hemoglobin signal changes o...

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Autores principales: Nagashima, Masako, Monden, Yukifumi, Dan, Ippeita, Dan, Haruka, Tsuzuki, Daisuke, Mizutani, Tsutomu, Kyutoku, Yasushi, Gunji, Yuji, Hirano, Daisuke, Taniguchi, Takamichi, Shimoizumi, Hideo, Momoi, Mariko Y., Watanabe, Eiju, Yamagata, Takanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215398/
https://www.ncbi.nlm.nih.gov/pubmed/25379431
http://dx.doi.org/10.1016/j.nicl.2014.09.001
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author Nagashima, Masako
Monden, Yukifumi
Dan, Ippeita
Dan, Haruka
Tsuzuki, Daisuke
Mizutani, Tsutomu
Kyutoku, Yasushi
Gunji, Yuji
Hirano, Daisuke
Taniguchi, Takamichi
Shimoizumi, Hideo
Momoi, Mariko Y.
Watanabe, Eiju
Yamagata, Takanori
author_facet Nagashima, Masako
Monden, Yukifumi
Dan, Ippeita
Dan, Haruka
Tsuzuki, Daisuke
Mizutani, Tsutomu
Kyutoku, Yasushi
Gunji, Yuji
Hirano, Daisuke
Taniguchi, Takamichi
Shimoizumi, Hideo
Momoi, Mariko Y.
Watanabe, Eiju
Yamagata, Takanori
author_sort Nagashima, Masako
collection PubMed
description The object of the current study is to explore the neural substrate for effects of atomoxetine (ATX) on inhibitory control in school-aged children with attention deficit hyperactivity disorder (ADHD) using functional near-infrared spectroscopy (fNIRS). We monitored the oxy-hemoglobin signal changes of sixteen ADHD children (6–14 years old) performing a go/no-go task before and 1.5 h after ATX or placebo administration, in a randomized, double-blind, placebo-controlled, crossover design. Sixteen age- and gender-matched normal controls without ATX administration were also monitored. In the control subjects, the go/no-go task recruited the right inferior and middle prefrontal gyri (IFG/MFG), and this activation was absent in pre-medicated ADHD children. The reduction of right IFG/MFG activation was acutely normalized after ATX administration but not placebo administration in ADHD children. These results are reminiscent of the neuropharmacological effects of methylphenidate to up-regulate reduced right IFG/MFG function in ADHD children during inhibitory tasks. As with methylphenidate, activation in the IFG/MFG could serve as an objective neuro-functional biomarker to indicate the effects of ATX on inhibitory control in ADHD children. This promising technique will enhance early clinical diagnosis and treatment of ADHD in children, especially in those with a hyperactivity/impulsivity phenotype.
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spelling pubmed-42153982014-11-06 Acute neuropharmacological effects of atomoxetine on inhibitory control in ADHD children: A fNIRS study Nagashima, Masako Monden, Yukifumi Dan, Ippeita Dan, Haruka Tsuzuki, Daisuke Mizutani, Tsutomu Kyutoku, Yasushi Gunji, Yuji Hirano, Daisuke Taniguchi, Takamichi Shimoizumi, Hideo Momoi, Mariko Y. Watanabe, Eiju Yamagata, Takanori Neuroimage Clin Article The object of the current study is to explore the neural substrate for effects of atomoxetine (ATX) on inhibitory control in school-aged children with attention deficit hyperactivity disorder (ADHD) using functional near-infrared spectroscopy (fNIRS). We monitored the oxy-hemoglobin signal changes of sixteen ADHD children (6–14 years old) performing a go/no-go task before and 1.5 h after ATX or placebo administration, in a randomized, double-blind, placebo-controlled, crossover design. Sixteen age- and gender-matched normal controls without ATX administration were also monitored. In the control subjects, the go/no-go task recruited the right inferior and middle prefrontal gyri (IFG/MFG), and this activation was absent in pre-medicated ADHD children. The reduction of right IFG/MFG activation was acutely normalized after ATX administration but not placebo administration in ADHD children. These results are reminiscent of the neuropharmacological effects of methylphenidate to up-regulate reduced right IFG/MFG function in ADHD children during inhibitory tasks. As with methylphenidate, activation in the IFG/MFG could serve as an objective neuro-functional biomarker to indicate the effects of ATX on inhibitory control in ADHD children. This promising technique will enhance early clinical diagnosis and treatment of ADHD in children, especially in those with a hyperactivity/impulsivity phenotype. Elsevier 2014-09-10 /pmc/articles/PMC4215398/ /pubmed/25379431 http://dx.doi.org/10.1016/j.nicl.2014.09.001 Text en © 2014 The Authors. Published by Elsevier Inc. All rights reserved. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Nagashima, Masako
Monden, Yukifumi
Dan, Ippeita
Dan, Haruka
Tsuzuki, Daisuke
Mizutani, Tsutomu
Kyutoku, Yasushi
Gunji, Yuji
Hirano, Daisuke
Taniguchi, Takamichi
Shimoizumi, Hideo
Momoi, Mariko Y.
Watanabe, Eiju
Yamagata, Takanori
Acute neuropharmacological effects of atomoxetine on inhibitory control in ADHD children: A fNIRS study
title Acute neuropharmacological effects of atomoxetine on inhibitory control in ADHD children: A fNIRS study
title_full Acute neuropharmacological effects of atomoxetine on inhibitory control in ADHD children: A fNIRS study
title_fullStr Acute neuropharmacological effects of atomoxetine on inhibitory control in ADHD children: A fNIRS study
title_full_unstemmed Acute neuropharmacological effects of atomoxetine on inhibitory control in ADHD children: A fNIRS study
title_short Acute neuropharmacological effects of atomoxetine on inhibitory control in ADHD children: A fNIRS study
title_sort acute neuropharmacological effects of atomoxetine on inhibitory control in adhd children: a fnirs study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215398/
https://www.ncbi.nlm.nih.gov/pubmed/25379431
http://dx.doi.org/10.1016/j.nicl.2014.09.001
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