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http://elar.urfu.ru/handle/10995/102308
Title: | Improving treatment of neurodevelopmental disorders: Recommendations based on preclinical studies |
Authors: | Homberg, J. R. Kyzar, E. J. Stewart, A. M. Nguyen, M. Poudel, M. K. Echevarria, D. J. Collier, A. D. Gaikwad, S. Klimenko, V. M. Norton, W. Pittman, J. Nakamura, S. Koshiba, M. Yamanouchi, H. Apryatin, S. A. Scattoni, M. L. Diamond, D. M. Ullmann, J. F. P. Parker, M. O. Brown, R. E. Song, C. Kalueff, A. V. |
Issue Date: | 2016 |
Publisher: | Taylor and Francis Ltd |
Citation: | Improving treatment of neurodevelopmental disorders: Recommendations based on preclinical studies / J. R. Homberg, E. J. Kyzar, A. M. Stewart, et al. — DOI 10.1517/17460441.2016.1115834 // Expert Opinion on Drug Discovery. — 2016. — Vol. 11. — Iss. 1. — P. 11-25. |
Abstract: | Introduction: Neurodevelopmental disorders (NDDs) are common and severely debilitating. Their chronic nature and reliance on both genetic and environmental factors makes studying NDDs and their treatment a challenging task.Areas covered: Herein, the authors discuss the neurobiological mechanisms of NDDs, and present recommendations on their translational research and therapy, outlined by the International Stress and Behavior Society. Various drugs currently prescribed to treat NDDs also represent a highly diverse group. Acting on various neurotransmitter and physiological systems, these drugs often lack specificity of action, and are commonly used to treat multiple other psychiatric conditions. There has also been relatively little progress in the development of novel medications to treat NDDs. Based on clinical, preclinical and translational models of NDDs, our recommendations cover a wide range of methodological approaches and conceptual strategies.Expert opinion: To improve pharmacotherapy and drug discovery for NDDs, we need a stronger emphasis on targeting multiple endophenotypes, a better dissection of genetic/epigenetic factors or "hidden heritability," and a careful consideration of potential developmental/trophic roles of brain neurotransmitters. The validity of animal NDD models can be improved through discovery of novel (behavioral, physiological and neuroimaging) biomarkers, applying proper environmental enrichment, widening the spectrum of model organisms, targeting developmental trajectories of NDD-related behaviors and comorbid conditions beyond traditional NDDs. While these recommendations cannot be addressed all in once, our increased understanding of NDD pathobiology may trigger innovative cross-disciplinary research expanding beyond traditional methods and concepts. © 2015 2015 Taylor & Francis. |
Keywords: | ADHD ANIMAL MODELS AUTISM NEURODEVELOPMENTAL DISORDERS TRANSLATIONAL RESEARCH AMPHETAMINE PLUS DEXAMPHETAMINE ARIPIPRAZOLE ATOMOXETINE BUSPIRONE CLONIDINE HALOPERIDOL LISDEXAMFETAMINE METHYLPHENIDATE NALTREXONE NEUROTRANSMITTER OLANZAPINE PIMOZIDE RISPERIDONE SEROTONIN UPTAKE INHIBITOR ZIPRASIDONE AGENTS INTERACTING WITH TRANSMITTER, HORMONE OR DRUG RECEPTORS BIOLOGICAL MARKER BEHAVIOR CHANGE CLINICAL ASSESSMENT CLINICAL EVALUATION COMORBIDITY ENDOPHENOTYPE ENVIRONMENTAL ENRICHMENT EPIGENETICS GENETIC ANALYSIS GENOTYPE ENVIRONMENT INTERACTION HEREDITY HERITABILITY HUMAN MENTAL DISEASE NEUROBIOLOGY NEUROIMAGING NONHUMAN PHENOTYPIC VARIATION PHYSIOLOGICAL PROCESS PRIORITY JOURNAL PRODROMAL SYMPTOM PSYCHOPHARMACOLOGY REVIEW STRATEGIC PLANNING TRANSLATIONAL RESEARCH TREATMENT INDICATION ANIMAL DISEASE MODEL DRUG DESIGN DRUG DEVELOPMENT GENETICS METABOLISM NEURODEVELOPMENTAL DISORDERS PATHOPHYSIOLOGY PROCEDURES ANIMALS BIOMARKERS DISEASE MODELS, ANIMAL DRUG DESIGN DRUG DISCOVERY ENDOPHENOTYPES HUMANS NEURODEVELOPMENTAL DISORDERS NEUROTRANSMITTER AGENTS TRANSLATIONAL MEDICAL RESEARCH |
URI: | http://elar.urfu.ru/handle/10995/102308 |
Access: | info:eu-repo/semantics/openAccess |
SCOPUS ID: | 84955215464 |
WOS ID: | 000368024100001 |
PURE ID: | ee542f12-a043-4bc9-b896-7503aa50791f 657641 |
ISSN: | 17460441 |
DOI: | 10.1517/17460441.2016.1115834 |
Appears in Collections: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
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