Multiphasic modulation of cholinergic interneurons by nigrostriatal afferents
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The motor and learning functions of the striatum are critically dependent on synaptic transmission from midbrain dopamine neurons and striatal cholinergic interneurons (CINs). Both neural populations alter their discharge in vivo in response to salient sensory stimuli, albeit in opposite directions. Whereas midbrain dopamine neurons respond to salient stimuli with a brief burst of activity, CINs exhibit a distinct pause in firing that is often followed by a period of increased excitability. Although this "pause-rebound" sensory response requires dopaminergic signaling, the precise mechanisms underlying the modulation of CIN firing by dopaminergic afferents remain unclear. Here, we show that phasic activation of nigrostriatal afferents in a mouse striatal slice preparation is sufficient to evoke a pause-rebound response in CINs. Using a combination of optogenetic, electrophysiological, and pharmacological approaches, we demonstrate that synaptically released dopamine inhibits CINs through type 2 dopamine receptors, while another unidentified transmitter mediates the delayed excitation. These findings imply that, in addition to their direct effects on striatal projection neurons, midbrain dopamine neurons indirectly modulate striatal output by dynamically controlling cholinergic tone. In addition, our data suggest that phasic dopaminergic activity may directly participate in the characteristic pause-rebound sensory response that CINs exhibit in vivo in response to salient and conditioned stimuli.
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Dopamine neurons projecting to ventral and dorsal striatum that express vGluT2 release glutamate onto striatal SPNs and CINs.
“dopamine neurons in the ventral midbrain projecting to ventral and dorsal striatum expressing the vGluT2 were confirmed, using optogenetic stimulation in brain slices, to release glutamate onto striatal SPNs and CINs.[108][109][110]”
From Synaptic and circuit functions of multitransmitter neurons in the mammalian brain (2023) · cites this paper as [109]
Dopamine, GABA, and glutamate released by DANs may elicit prolonged waves of postsynaptic effects, from millisecond excitability changes to tens-of-seconds biochemical signaling and excitability.
“the dopamine, GABA, and glutamate released by DANs may elicit prolonged waves of postsynaptic effects, cascading from the millisecond changes in excitability triggered by ionotropic receptors, to the tens of seconds on biochemical signaling and excitability 109,115,122,123 (Figure 3A).”
From Synaptic and circuit functions of multitransmitter neurons in the mammalian brain (2023) · cites this paper as [109]
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References 69 · Cited by 130
- Authors
- Straub, C., Tritsch, N. X., Hagan, N. A., Gu, C., & Sabatini, B. L.
- Affiliations
- Howard Hughes Medical Institute (US)
- Harvard University (US)
- Venue
- Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2014-06-18
- Volume
- 34
- Issue
- 25
- Pages
- 8557-8569
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC4061393
- OpenAlex
- W1988578216
- Cited by
- 130
- References
- 69
- Citations by year
- 2026: 7 · 2025: 16 · 2024: 4 · 2023: 18 · 2022: 9 · 2021: 13 · 2020: 9 · 2019: 8 · 2018: 9 · 2017: 10 · 2016: 15 · 2015: 9 · 2014: 3
- FWCI
- 5.64
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Neuroscience (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Public Health Service (R01NSO64583)
- National Institute of Neurological Disorders and Stroke (R01NS046579, R37NS046579, NS046579)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Neurology › Neurological disorders and treatments
- Keywords
- striatal cholinergic interneurons, midbrain dopaminergic neurons, dopamine D2 receptor, cholinergic tone, striatal output, optogenetic stimulation
- MeSH terms
- Action Potentials, Afferent Pathways, Animals, Corpus Striatum, Female, Interneurons, Male, Mice, Transgenic, Substantia Nigra, Mice, Gene Knock-In Techniques, Cholinergic Neurons
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