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Access to the CNS: Biomarker Strategies for Dopaminergic Treatments

Despite substantial research carried out over the last decades, it remains difficult to understand the wide range of pharmacological effects of dopaminergic agents. The dopaminergic system is involved in several neurological disorders, such as Parkinson’s disease and schizophrenia. This complex syst...

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Autores principales: van den Brink, Willem Johan, Palic, Semra, Köhler, Isabelle, de Lange, Elizabeth Cunera Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814527/
https://www.ncbi.nlm.nih.gov/pubmed/29450650
http://dx.doi.org/10.1007/s11095-017-2333-x
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author van den Brink, Willem Johan
Palic, Semra
Köhler, Isabelle
de Lange, Elizabeth Cunera Maria
author_facet van den Brink, Willem Johan
Palic, Semra
Köhler, Isabelle
de Lange, Elizabeth Cunera Maria
author_sort van den Brink, Willem Johan
collection PubMed
description Despite substantial research carried out over the last decades, it remains difficult to understand the wide range of pharmacological effects of dopaminergic agents. The dopaminergic system is involved in several neurological disorders, such as Parkinson’s disease and schizophrenia. This complex system features multiple pathways implicated in emotion and cognition, psychomotor functions and endocrine control through activation of G protein-coupled dopamine receptors. This review focuses on the system-wide effects of dopaminergic agents on the multiple biochemical and endocrine pathways, in particular the biomarkers (i.e., indicators of a pharmacological process) that reflect these effects. Dopaminergic treatments developed over the last decades were found to be associated with numerous biochemical pathways in the brain, including the norepinephrine and the kynurenine pathway. Additionally, they have shown to affect peripheral systems, for example the hypothalamus-pituitary-adrenal (HPA) axis. Dopaminergic agents thus have a complex and broad pharmacological profile, rendering drug development challenging. Considering the complex system-wide pharmacological profile of dopaminergic agents, this review underlines the needs for systems pharmacology studies that include: i) proteomics and metabolomics analysis; ii) longitudinal data evaluation and mathematical modeling; iii) pharmacokinetics-based interpretation of drug effects; iv) simultaneous biomarker evaluation in the brain, the cerebrospinal fluid (CSF) and plasma; and v) specific attention to condition-dependent (e.g., disease) pharmacology. Such approach is considered essential to increase our understanding of central nervous system (CNS) drug effects and substantially improve CNS drug development.
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spelling pubmed-58145272018-02-26 Access to the CNS: Biomarker Strategies for Dopaminergic Treatments van den Brink, Willem Johan Palic, Semra Köhler, Isabelle de Lange, Elizabeth Cunera Maria Pharm Res Expert Review Despite substantial research carried out over the last decades, it remains difficult to understand the wide range of pharmacological effects of dopaminergic agents. The dopaminergic system is involved in several neurological disorders, such as Parkinson’s disease and schizophrenia. This complex system features multiple pathways implicated in emotion and cognition, psychomotor functions and endocrine control through activation of G protein-coupled dopamine receptors. This review focuses on the system-wide effects of dopaminergic agents on the multiple biochemical and endocrine pathways, in particular the biomarkers (i.e., indicators of a pharmacological process) that reflect these effects. Dopaminergic treatments developed over the last decades were found to be associated with numerous biochemical pathways in the brain, including the norepinephrine and the kynurenine pathway. Additionally, they have shown to affect peripheral systems, for example the hypothalamus-pituitary-adrenal (HPA) axis. Dopaminergic agents thus have a complex and broad pharmacological profile, rendering drug development challenging. Considering the complex system-wide pharmacological profile of dopaminergic agents, this review underlines the needs for systems pharmacology studies that include: i) proteomics and metabolomics analysis; ii) longitudinal data evaluation and mathematical modeling; iii) pharmacokinetics-based interpretation of drug effects; iv) simultaneous biomarker evaluation in the brain, the cerebrospinal fluid (CSF) and plasma; and v) specific attention to condition-dependent (e.g., disease) pharmacology. Such approach is considered essential to increase our understanding of central nervous system (CNS) drug effects and substantially improve CNS drug development. Springer US 2018-02-15 2018 /pmc/articles/PMC5814527/ /pubmed/29450650 http://dx.doi.org/10.1007/s11095-017-2333-x Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Expert Review
van den Brink, Willem Johan
Palic, Semra
Köhler, Isabelle
de Lange, Elizabeth Cunera Maria
Access to the CNS: Biomarker Strategies for Dopaminergic Treatments
title Access to the CNS: Biomarker Strategies for Dopaminergic Treatments
title_full Access to the CNS: Biomarker Strategies for Dopaminergic Treatments
title_fullStr Access to the CNS: Biomarker Strategies for Dopaminergic Treatments
title_full_unstemmed Access to the CNS: Biomarker Strategies for Dopaminergic Treatments
title_short Access to the CNS: Biomarker Strategies for Dopaminergic Treatments
title_sort access to the cns: biomarker strategies for dopaminergic treatments
topic Expert Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814527/
https://www.ncbi.nlm.nih.gov/pubmed/29450650
http://dx.doi.org/10.1007/s11095-017-2333-x
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