The DOI matches its Crossref record; 132 of the 132 references it cites were found in a registry or an index.
The Striatal Balancing Act in Drug Addiction: Distinct Roles of Direct and Indirect Pathway Medium Spiny Neurons
Open accessAbstract
The striatum plays a key role in mediating the acute and chronic effects of addictive drugs, with drugs of abuse causing long-lasting molecular and cellular alterations in both dorsal striatum and nucleus accumbens (ventral striatum). Despite the wealth of research on the biological actions of abused drugs in striatum, until recently, the distinct roles of the striatum's two major subtypes of medium spiny neurons (MSNs) in drug addiction remained elusive. Recent advances in cell-type-specific technologies, including fluorescent reporter mice, transgenic, or knockout mice, and viral-mediated gene transfer, have advanced the field toward a more comprehensive understanding of the two MSN subtypes in the long-term actions of drugs of abuse. Here we review progress in defining the distinct molecular and functional contributions of the two MSN subtypes in mediating addiction.
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Social reward requires coordinated activity of nucleus accumbens oxytocin and serotonin
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Dopamine Signaling in reward-related behaviors
Baik, J.-H. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00152 · Cited by 531
The changing opioid crisis: development, challenges and opportunities
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Metadata
- Authors
- Lobo, M. K., & Nestler, E. J.
- Venue
- Frontiers in Neuroanatomy
- Publisher
- Frontiers Media SA
- Published
- 2011
- Volume
- 5
- Pages
- 41-41
- ISSN
- 1662-5129 (ISSN-L)
- OpenAlex
- W2023637370
- Cited by
- 381
- References
- 132
- FWCI
- 7.86
- Type
- journal article
- Language
- en
- Open access
- gold
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- Lobo, M. K., & Nestler, E. J. (2011). The Striatal Balancing Act in Drug Addiction: Distinct Roles of Direct and Indirect Pathway Medium Spiny Neurons. Frontiers in Neuroanatomy. https://doi.org/10.3389/fnana.2011.00041
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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