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Systemic neurotransmitter responses to clinically approved and experimental neuropsychiatric drugs

Neuropsychiatric disorders are the third leading cause of global disease burden. Current pharmacological treatment for these disorders is inadequate, with often insufficient efficacy and undesirable side effects. One reason for this is that the links between molecular drug action and neurobehavioral...

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Autores principales: Noori, Hamid R., Mervin, Lewis H., Bokharaie, Vahid, Durmus, Özlem, Egenrieder, Lisamon, Fritze, Stefan, Gruhlke, Britta, Reinhardt, Giulia, Schabel, Hans-Hendrik, Staudenmaier, Sabine, Logothetis, Nikos K., Bender, Andreas, Spanagel, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224407/
https://www.ncbi.nlm.nih.gov/pubmed/30410047
http://dx.doi.org/10.1038/s41467-018-07239-1
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author Noori, Hamid R.
Mervin, Lewis H.
Bokharaie, Vahid
Durmus, Özlem
Egenrieder, Lisamon
Fritze, Stefan
Gruhlke, Britta
Reinhardt, Giulia
Schabel, Hans-Hendrik
Staudenmaier, Sabine
Logothetis, Nikos K.
Bender, Andreas
Spanagel, Rainer
author_facet Noori, Hamid R.
Mervin, Lewis H.
Bokharaie, Vahid
Durmus, Özlem
Egenrieder, Lisamon
Fritze, Stefan
Gruhlke, Britta
Reinhardt, Giulia
Schabel, Hans-Hendrik
Staudenmaier, Sabine
Logothetis, Nikos K.
Bender, Andreas
Spanagel, Rainer
author_sort Noori, Hamid R.
collection PubMed
description Neuropsychiatric disorders are the third leading cause of global disease burden. Current pharmacological treatment for these disorders is inadequate, with often insufficient efficacy and undesirable side effects. One reason for this is that the links between molecular drug action and neurobehavioral drug effects are elusive. We use a big data approach from the neurotransmitter response patterns of 258 different neuropsychiatric drugs in rats to address this question. Data from experiments comprising 110,674 rats are presented in the Syphad database [www.syphad.org]. Chemoinformatics analyses of the neurotransmitter responses suggest a mismatch between the current classification of neuropsychiatric drugs and spatiotemporal neurostransmitter response patterns at the systems level. In contrast, predicted drug–target interactions reflect more appropriately brain region related neurotransmitter response. In conclusion the neurobiological mechanism of neuropsychiatric drugs are not well reflected by their current classification or their chemical similarity, but can be better captured by molecular drug–target interactions.
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spelling pubmed-62244072018-11-13 Systemic neurotransmitter responses to clinically approved and experimental neuropsychiatric drugs Noori, Hamid R. Mervin, Lewis H. Bokharaie, Vahid Durmus, Özlem Egenrieder, Lisamon Fritze, Stefan Gruhlke, Britta Reinhardt, Giulia Schabel, Hans-Hendrik Staudenmaier, Sabine Logothetis, Nikos K. Bender, Andreas Spanagel, Rainer Nat Commun Article Neuropsychiatric disorders are the third leading cause of global disease burden. Current pharmacological treatment for these disorders is inadequate, with often insufficient efficacy and undesirable side effects. One reason for this is that the links between molecular drug action and neurobehavioral drug effects are elusive. We use a big data approach from the neurotransmitter response patterns of 258 different neuropsychiatric drugs in rats to address this question. Data from experiments comprising 110,674 rats are presented in the Syphad database [www.syphad.org]. Chemoinformatics analyses of the neurotransmitter responses suggest a mismatch between the current classification of neuropsychiatric drugs and spatiotemporal neurostransmitter response patterns at the systems level. In contrast, predicted drug–target interactions reflect more appropriately brain region related neurotransmitter response. In conclusion the neurobiological mechanism of neuropsychiatric drugs are not well reflected by their current classification or their chemical similarity, but can be better captured by molecular drug–target interactions. Nature Publishing Group UK 2018-11-08 /pmc/articles/PMC6224407/ /pubmed/30410047 http://dx.doi.org/10.1038/s41467-018-07239-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Noori, Hamid R.
Mervin, Lewis H.
Bokharaie, Vahid
Durmus, Özlem
Egenrieder, Lisamon
Fritze, Stefan
Gruhlke, Britta
Reinhardt, Giulia
Schabel, Hans-Hendrik
Staudenmaier, Sabine
Logothetis, Nikos K.
Bender, Andreas
Spanagel, Rainer
Systemic neurotransmitter responses to clinically approved and experimental neuropsychiatric drugs
title Systemic neurotransmitter responses to clinically approved and experimental neuropsychiatric drugs
title_full Systemic neurotransmitter responses to clinically approved and experimental neuropsychiatric drugs
title_fullStr Systemic neurotransmitter responses to clinically approved and experimental neuropsychiatric drugs
title_full_unstemmed Systemic neurotransmitter responses to clinically approved and experimental neuropsychiatric drugs
title_short Systemic neurotransmitter responses to clinically approved and experimental neuropsychiatric drugs
title_sort systemic neurotransmitter responses to clinically approved and experimental neuropsychiatric drugs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224407/
https://www.ncbi.nlm.nih.gov/pubmed/30410047
http://dx.doi.org/10.1038/s41467-018-07239-1
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