Anxiolytic drug discovery: What are the novel approaches and how can we improve them?
Abstract
INTRODUCTION: Contemporary biological psychiatry uses experimental (animal) models to increase our understanding of affective disorder pathogenesis. Despite the well-recognized spectrum nature of affective disorders, modern anxiolytic drug discovery mainly targets specific pathways and molecular determinants within a single phenotypic domain. However, greater understanding of the integrative mechanisms and pathogenesis is essential in order to develop new effective therapies. AREAS COVERED: In this review, the authors emphasize the importance of a 'domain interplay-oriented' approach to experimental affective research. They also highlight the need to expand the scope of anxiolytic drug targets to better understand the pathogenesis of anxiety-spectrum disorders. EXPERT OPINION: There is the potential to markedly improve the utility of animal models for affective disorders. First, the authors suggest that one such way would be by analyzing the systems of several domains and their interplay to better understand disease pathogenesis. Further, it could also be improved by expanding the range of model species and by extending the spectrum of anxiolytic drug targets; this would help to focus on emerging and unconventional systems to better develop new therapies.
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Basic anxiety-related processes are increasingly being identified and successfully replicated in other species including humans.
“With these precautions in mind, basic anxietyrelated processes are increasingly being identified and successfully replicated in other species including humans (Stewart et al. 2014;Mohammad et al. 2016).”
From Novel pharmacological targets in drug development for the treatment of anxiety and anxiety-related disorders (2019) · cites this paper as Stewart et al. 2014
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Developing ‘integrative’ zebrafish models of behavioral and metabolic disorders
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“Largely known for its powerful influence on the regulation of social behavior in several species [47,52,134] (including humans [134-136]), continuously growing research further implicates OT as a robust anxiolytic [137-139].”
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Sartori, S. B., & Singewald, N. (2019) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2019.107402 · Cited by 236 · see citing works
Stewart, A. M., Roy, S., Wong, K., Gaikwad, S., Chung, K. M., & Kalueff, A. V. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.08.037 · Cited by 44 · see citing works
Self-citation
- Authors
- Stewart, A. M., & Kalueff, A. V.
- Affiliations
- University of Pittsburgh (US)
- Venue
- Expert Opinion on Drug Discovery
- Publisher
- Informa UK Limited
- Published
- 2013-11-09
- Volume
- 9
- Issue
- 1
- Pages
- 15-26
- ISSN
- 1746-0441 (ISSN-L)
- 1746-045X
- OpenAlex
- W2116099374
- Semantic Scholar
- c57afc9357d124dbc08a7a2fe6bebc9a2379ae7f
- Cited by
- 22
- References
- 175
- Citations by year
- 2025: 1 · 2022: 1 · 2019: 1 · 2017: 2 · 2016: 4 · 2015: 6 · 2014: 7
- FWCI
- 0.58
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Expert Opinion on Drug Discovery (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes
- Keywords
- anxiety disorders, mood disorders, animal models of anxiety, pathogenesis, model organisms, psychiatric drug development
- MeSH terms
- Animals, Disease Models, Animal, Humans, Anti-Anxiety Agents, Drug Discovery
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