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Neuropeptide receptor ligands as drugs for psychiatric diseases: the end of the beginning?
Abstract
The search for novel drugs for treating psychiatric disorders is driven by the growing medical need to improve on the effectiveness and side-effect profile of currently available therapies. Given the wealth of preclinical data supporting the role of neuropeptides in modulating behaviour, pharmaceutical companies have been attempting to target neuropeptide receptors for over two decades. However, clinical studies with synthetic neuropeptide ligands have been unable to confirm the promise predicted by studies in animal models. Here, we analyse preclinical and clinical results for neuropeptide receptor ligands that have been studied in clinical trials for psychiatric diseases, including agents that target the receptors for tachykinins, corticotropin-releasing factor, vasopressin and neurotensin, and suggest new ways to exploit the full potential of these candidate drugs.
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“Additionally, no clinical studies to date have found efficacy of CRF 1 receptor antagonists for the treatment of other stress-related psychiatric disorders, such as major depression, generalized anxiety disorder, social anxiety, or posttraumatic stress disorder (Griebel and Holsboer, 2012;Dunlop et al., 2017).”
From Drug Addiction: Hyperkatifeia/Negative Reinforcement as a Framework for Medications Development (2021) · cites this paper as Griebel and Holsboer, 2012
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Metadata
- Authors
- Griebel, G., & Holsboer, F.
- Affiliations
- Sanofi (France) (FR)
- Max Planck Institute of Psychiatry (DE)
- Corresponding author
- Griebel, Guy
- ORCID
- Griebel, Guy
- Venue
- Nature Reviews Drug Discovery
- Published
- 2012-05-18
- Volume
- 11
- Issue
- 6
- Pages
- 462-478
- ISSN
- 1474-1776 (ISSN-L)
- 1474-1784
- OpenAlex
- W2089617519
- Cited by
- 194
- References
- 176
- Citations by year
- 2026: 5 · 2025: 5 · 2024: 8 · 2023: 12 · 2022: 9 · 2021: 14 · 2020: 9 · 2019: 10 · 2018: 16 · 2017: 13 · 2016: 20 · 2015: 22 · 2014: 19 · 2013: 23 · 2012: 9
- FWCI
- 2.50
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Drug Discovery (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
- Physical Sciences › Chemistry › Organic Chemistry › Chemical Synthesis and Analysis
- Keywords
- psychiatric drug development, tachykinins, corticotropin-releasing factor, vasopressin, neurotensin, clinical translation, adverse effects
- MeSH terms
- Animals, Mental Disorders, Corticotropin-Releasing Hormone, Humans, Ligands, Neurotensin, Psychotropic Drugs, Vasopressins, Tachykinins, Drug Delivery Systems, Receptors, Vasopressin, Receptors, Neuropeptide, Receptors, Corticotropin-Releasing Hormone, Receptors, Neurotensin, Receptors, Tachykinin
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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