The role of neuropeptide Y (NPY) in alcohol and drug abuse disorders
Abstract
Neuropeptide Y (NPY) is a neuromodulator that is widely expressed throughout the central nervous system (CNS) and which is cosecreted with classic neurotransmitters including GABA and glutamate. There is a long history of research implicating a role for NPY in modulating neurobiological responses to alcohol (ethanol) as well as other drugs of abuse. Both ethanol exposure and withdrawal from chronic ethanol have been shown to produce changes in NPY and NPY receptor protein levels and mRNA expression in the CNS. Importantly, manipulations of NPY Y1 and Y2 receptor signaling have been shown to alter ethanol consumption and self-administration in a brain region-specific manner, with Y1 receptor activation and Y2 receptor blockade in regions of the extended amygdala promoting robust reductions of ethanol intake. Similar observations have been made in studies examining neurobiological responses to nicotine, psychostimulants, and opioids. When taken together with observations of potential genetic linkage between the NPY system and the human alcohol abuse disorders, NPY represents a promising target for treating problematic alcohol and drug use, and in protecting individuals from relapse during abstinence.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
For opioids, NPY can potentiate their acute rewarding effects.
“For opioids, NPY can potentiate their acute rewarding effects (Robinson and Thiele, 2017).”
From Drug Addiction: Hyperkatifeia/Negative Reinforcement as a Framework for Medications Development (2021) · cites this paper as Robinson and Thiele, 2017
Cites
Gilpin, N. W., Misra, K., & Koob, G. F. (2008) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2008.04.006 · Cited by 97 · see citing works
Neuropeptide-Y in the paraventricular nucleus increases ethanol self-administration
Kelley, S. P., Nannini, M. A., Bratt, A. M., & Hodge, C. W. (2001) · Peptides · doi:10.1016/s0196-9781(01)00361-8 · Cited by 88 · see citing works
Gene expression changes following extinction testing in a heroin behavioral incubation model
Kuntz-Melcavage, K. L., Brucklacher, R. M., Grigson, P. S., Freeman, W. M., & Vrana, K. E. (2009) · BMC Neuroscience · doi:10.1186/1471-2202-10-95 · Cited by 53 · see citing works
Maric, T., Tobin, S., Quinn, T., & Shalev, U. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.06.023 · Cited by 33 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Neurobiology of opioid addiction: Opponent process, hyperkatifeia, and negative reinforcement
Koob, G. F. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.05.023 · Cited by 477 · see citing works
Gut Bacteria and Neurotransmitters
Dicks, L. M. T. (2022) · Microorganisms · doi:10.3390/microorganisms10091838 · Cited by 482 · see citing works
Drug Addiction: Hyperkatifeia/Negative Reinforcement as a Framework for Medications Development
Koob, G. F. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000083 · Cited by 337 · see citing works
Off-label and investigational drugs in the treatment of alcohol use disorder: A critical review
Fischler, P. V., Soyka, M., Seifritz, E., & Mutschler, J. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.927703 · Cited by 34 · see citing works
- Authors
- Robinson, S. L., & Thiele, T. E.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- Corresponding author
- Thiele, Todd E.
- Venue
- International Review of Neurobiology
- Publisher
- Elsevier
- Published
- 2017
- Volume
- 136
- Pages
- 177-197
- ISSN
- 0074-7742 (ISSN-L)
- OpenAlex
- W2740461424
- Cited by
- 75
- References
- 4
- Citations by year
- 2026: 6 · 2025: 6 · 2024: 7 · 2023: 7 · 2022: 11 · 2021: 12 · 2020: 13 · 2019: 10 · 2018: 3
- FWCI
- 14.70
- Type
- book chapter
- Language
- en
- Open access
- closed
- Locations
- International review of neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Alcohol Abuse and Alcoholism
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- neuropeptide Y, alcoholism, drug abuse, ethanol self-administration, ethanol withdrawal, NPY Y1 receptor, NPY Y2 receptor, extended amygdala, nicotine, psychostimulants, opioids, relapse, genetic linkage, neuromodulation
- MeSH terms
- Alcohol Drinking, Animals, Humans, Opioid-Related Disorders, Neuropeptide Y, Tobacco Use Disorder, Receptors, Neuropeptide Y, Amphetamine-Related Disorders, Cocaine-Related Disorders, Alcohol-Related Disorders
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 ›
Are you an author, or do you see a problem with this page? Request a review