Synaptic plasticity in the mesolimbic dopamine system
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Long-term potentiation (LTP) and long-term depression (LTD) are thought to be critical mechanisms that contribute to the neural circuit modifications that mediate all forms of experience-dependent plasticity. It has, however, been difficult to demonstrate directly that experience causes long-lasting changes in synaptic strength and that these mediate changes in behaviour. To address these potential functional roles of LTP and LTD, we have taken advantage of the powerful in vivo effects of drugs of abuse that exert their behavioural effects in large part by acting in the nucleus accumbens (NAc) and ventral tegmental area (VTA); the two major components of the mesolimbic dopamine system. Our studies suggest that in vivo drugs of abuse such as cocaine cause long-lasting changes at excitatory synapses in the NAc and VTA owing to activation of the mechanisms that underlie LTP and LTD in these structures. Thus, administration of drugs of abuse provides a distinctive model for further investigating the mechanisms and functions of synaptic plasticity in brain regions that play important roles in the control of motivated behaviour, and one with considerable practical implications.
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Early drug-evoked changes in the properties of excitatory synapses on dopamine cells can be very long-lasting and are followed by many additional synaptic modifications in related structures.
“These early drug-evoked changes in the properties of excitatory synapses on dopamine cells can be very long-lasting and are followed by many additional synaptic modifications in related structures.”
From NMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD). (2012) · cites this paper as Thomas and Malenka 2003
In the nucleus accumbens, chronic (5-d) administration of cocaine triggers an internalization of AMPARs in medium spiny neurons, a change that occludes the subsequent synaptic induction of NMDAR-dependent LTD.
“For example, in the nucleus accumbens chronic (5-d) administration of cocaine triggers an internalization of AMPARs in medium spiny neurons, a change that occludes the subsequent synaptic induction of NMDARdependent LTD (Thomas and Malenka 2003;Kauer and Malenka 2007;Wolf and Ferrario 2010).”
From NMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD). (2012) · cites this paper as Thomas and Malenka 2003
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References 26 · Cited by 137
- Authors
- Thomas, M. J., & Malenka, R. C.
- Affiliations
- University of Minnesota (US)
- Stanford Medicine (US)
- Corresponding author
- Malenka, Robert C.
- Venue
- Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences
- Publisher
- The Royal Society
- Published
- 2003-04-29
- Volume
- 358
- Issue
- 1432
- Pages
- 815-819
- ISSN
- 0962-8436 (ISSN-L)
- 1471-2970
- PMC
- PMC1693149
- OpenAlex
- W1923888830
- Cited by
- 137
- References
- 26
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 5 · 2023: 1 · 2022: 1 · 2021: 2 · 2020: 3 · 2019: 3 · 2018: 6 · 2017: 3 · 2016: 7 · 2015: 7 · 2014: 6 · 2013: 5 · 2012: 11
- FWCI
- 3.01
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Philosophical Transactions of the Royal Society B Biological Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (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
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- synaptic plasticity, mesolimbic dopamine system, long-term potentiation, long-term depression, nucleus accumbens, ventral tegmental area, drugs of abuse, cocaine, excitatory synapses, experience-dependent plasticity, motivated behavior, addiction
- MeSH terms
- Animals, Cocaine, Dopamine, Limbic System, Mesencephalon, Neuronal Plasticity, Neurons, Nucleus Accumbens, Synapses, Long-Term Potentiation, Dopamine Uptake Inhibitors
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