Characteristics of fast-spiking neurons in the striatum of behaving monkeys

•Fast-spiking neurons (FSNs) were differentiated from others by their spike shapes.•FSNs and phasically active neurons (PANs) encoded actions and outcomes similarly.•Discharge selectivity for actions and outcomes was higher in PANs than in FSNs.•FSNs showed high-frequency and less-bursty firings, bu...

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Veröffentlicht in:Neuroscience research 2016-04, Vol.105, p.2-18
Hauptverfasser: Yamada, Hiroshi, Inokawa, Hitoshi, Hori, Yukiko, Pan, Xiaochuan, Matsuzaki, Ryuichi, Nakamura, Kae, Samejima, Kazuyuki, Shidara, Munetaka, Kimura, Minoru, Sakagami, Masamichi, Minamimoto, Takafumi
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Sprache:eng
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Zusammenfassung:•Fast-spiking neurons (FSNs) were differentiated from others by their spike shapes.•FSNs and phasically active neurons (PANs) encoded actions and outcomes similarly.•Discharge selectivity for actions and outcomes was higher in PANs than in FSNs.•FSNs showed high-frequency and less-bursty firings, but PANs did not.•FSNs may enhance discharge selectivity of the postsynaptic output neurons (PANs). Inhibitory interneurons are the fundamental constituents of neural circuits that organize network outputs. The striatum as part of the basal ganglia is involved in reward-directed behaviors. However, the role of the inhibitory interneurons in this process remains unclear, especially in behaving monkeys. We recorded the striatal single neuron activity while monkeys performed reward-directed hand or eye movements. Presumed parvalbumin-containing GABAergic interneurons (fast-spiking neurons, FSNs) were identified based on narrow spike shapes in three independent experiments, though they were a small population (4.2%, 42/997). We found that FSNs are characterized by high-frequency and less-bursty discharges, which are distinct from the basic firing properties of the presumed projection neurons (phasically active neurons, PANs). Besides, the encoded information regarding actions and outcomes was similar between FSNs and PANs in terms of proportion of neurons, but the discharge selectivity was higher in PANs than that of FSNs. The coding of actions and outcomes in FSNs and PANs was consistently observed under various behavioral contexts in distinct parts of the striatum (caudate nucleus, putamen, and anterior striatum). Our results suggest that FSNs may enhance the discharge selectivity of postsynaptic output neurons (PANs) in encoding crucial variables for a reward-directed behavior.
ISSN:0168-0102
1872-8111
DOI:10.1016/j.neures.2015.10.003