Neuropeptide regulation of fear and anxiety: Implications of cholecystokinin, endogenous opioids, and neuropeptide Y
Open accessAbstract
The neural circuitry of fear likely underlies anxiety and fear-related disorders such as specific and social phobia, panic disorder, and posttraumatic stress disorder. The primary pharmacological treatments currently utilized for these disorders include benzodiazepines, which act on the GABAergic receptor system, and antidepressants, which modulate the monamine systems. However, recent work on the regulation of fear neural circuitry suggests that specific neuropeptide modulation of this system is of critical importance. Recent reviews have examined the roles of the hypothalamic-pituitary-adrenal axis neuropeptides as well as the roles of neurotrophic factors in regulating fear. The present review, instead, will focus on three neuropeptide systems which have received less attention in recent years but which are clearly involved in regulating fear and its extinction. The endogenous opioid system, particularly activating the μ opioid receptors, has been demonstrated to regulate fear expression and extinction, possibly through functioning as an error signal within the ventrolateral periaqueductal gray to mark unreinforced conditioned stimuli. The cholecystokinin (CCK) system initially led to much excitement through its potential role in panic disorder. More recent work in the CCK neuropeptide pathway suggests that it may act in concordance with the endogenous cannabinoid system in the modulation of fear inhibition and extinction. Finally, older as well as very recent data suggests that neuropeptide Y (NPY) may play a very interesting role in counteracting stress effects, enhancing extinction, and enhancing resilience in fear and stress preclinical models. Future work in understanding the mechanisms of neuropeptide functioning, particularly within well-known behavioral circuits, are likely to provide fascinating new clues into the understanding of fear behavior as well as suggesting novel therapeutics for treating disorders of anxiety and fear dysregulation.
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Several genes implicated in cocaine withdrawal (e.g., Nrgn, Cck, Rab3a) have widely known neuronal function.
“several genes implicated in cocaine withdrawal for example, Nrgn61, Cck62 or Rab3a63 (which also change in more than one cluster) have widely known neuronal function.”
From Cell type-specific transcriptional programs in mouse prefrontal cortex during adolescence and addiction (2019) · cites this paper as [62]
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References 136 · Cited by 155
- Authors
- Bowers, M. E., Choi, D. C., & Ressler, K. J.
- Affiliations
- Emory University (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Ressler, Kerry J.
- Venue
- Physiology & Behavior
- Publisher
- Elsevier BV
- Published
- 2012-12
- Volume
- 107
- Issue
- 5
- Pages
- 699-710
- ISSN
- 0031-9384 (ISSN-L)
- PMC
- PMC3532931
- OpenAlex
- W1984917106
- Cited by
- 155
- References
- 136
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 9 · 2023: 14 · 2022: 13 · 2021: 15 · 2020: 6 · 2019: 12 · 2018: 6 · 2017: 8 · 2016: 12 · 2015: 11 · 2014: 16 · 2013: 22 · 2012: 4
- FWCI
- 1.79
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Physiology & Behavior (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health
- National Institute of Mental Health (F32MH085443, R01MH096764, R01MH071537, F31MH097397)
- National Institute on Drug Abuse (R01DA01962, R01DA019624)
- National Center for Research Resources (P51RR000165)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- fear, anxiety, neuropeptides, cholecystokinin, endogenous opioids, mu-opioid receptor, neuropeptide Y, fear extinction, fear inhibition, ventrolateral periaqueductal gray, panic disorder, post-traumatic stress disorder, social anxiety disorder, stress resilience
- MeSH terms
- Animals, Anxiety, Brain, Cholecystokinin, Fear, Humans, Neuropeptide Y, Opioid Peptides
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