Unraveling glutamate–opioid receptor interactions using high-resolution electron microscopy: Implications for addiction-related processes
Open accessAbstract
Adaptive responses in glutamate and opioid receptor systems in limbic circuits are emerging as a critical component of the neural plasticity induced by chronic use of abused substances. The present commentary reviews findings from neuroanatomical studies, with superior spatial resolution, that support a cellular basis for prominent interactions of glutamate and opioid receptor systems in preclinical models of drug addiction. The review begins by highlighting the advantages of high-resolution electron microscopic immunohistochemistry for unraveling receptor interactions at the synapse. With an emphasis on a recent publication describing the anatomical relationship between the μ-opioid receptor (MOR) and the AMPA-GluR2 subunit (Beckerman, M. A., and Glass, M. J., 2011. Ultrastructural relationship between the AMPA-GluR2 receptor subunit and the mu-opioid receptor in the mouse central nucleus of the amygdala. Exp Neurol), we review the anatomical evidence for opioid-induced neural plasticity of glutamate receptors in selected brain circuits that are key integrative substrates in the brain's motivational system. The findings stress the importance of glutamate-opioid interactions as important neural mediators of adaptations to chronic use of abused drugs, particularly within the amygdaloid complex.
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Opioids interact with other addiction-related neurochemical systems, including dopamine and glutamate, though these interactions do not entirely explain the role of opioids in addiction.
“Opioids also interact with other addiction-related neurochemical systems, including DA and glutamate, though these interactions do not entirely explain the role of opioids in addiction (Dichiara and Imperato 1988; Johnson and North 1992; Scavone et al 2011).”
From The behavioral, anatomical and pharmacological parallels between social attachment, love and addiction (2012) · cites this paper as Scavone et al 2011
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References 99 · Cited by 16
- Authors
- Scavone, J. L., Asan, E., & Van Bockstaele, E. J.
- Affiliations
- Thomas Jefferson University (US)
- University of Würzburg (DE)
- ORCID
- Asan, Esther
- Venue
- Experimental Neurology
- Publisher
- Elsevier BV
- Published
- 2011-06
- Volume
- 229
- Issue
- 2
- Pages
- 207-213
- ISSN
- 0014-4886 (ISSN-L)
- PMC
- PMC3274957
- OpenAlex
- W1969526865
- Cited by
- 16
- References
- 99
- Citations by year
- 2023: 1 · 2022: 1 · 2021: 2 · 2020: 1 · 2019: 2 · 2018: 1 · 2017: 3 · 2016: 1 · 2015: 1 · 2014: 2 · 2012: 1
- FWCI
- 0.40
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Experimental Neurology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Drug Abuse (R01DA009082)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Keywords
- mu-opioid receptor, synaptic ultrastructure, drug addiction, neuroplasticity, amygdala, limbic circuits, motivation system, chronic drug use
- MeSH terms
- Amygdala, Animals, Microscopy, Electron, Receptors, Opioid, mu, Receptors, AMPA, Mice
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