Yosuke Saga
Tamagawa University
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Featured researches published by Yosuke Saga.
European Journal of Neuroscience | 2011
Yosuke Saga; Yoshihiro Hirata; Daisuke Takahara; Kenichi Inoue; Shigehiro Miyachi; Atsushi Nambu; Jun Tanji; Masahiko Takada; Eiji Hoshi
We examined the organization of multisynaptic projections from the basal ganglia (BG) to the dorsal premotor area in macaques. After injection of the rabies virus into the rostral sector of the caudal aspect of the dorsal premotor area (F2r) and the caudal sector of the caudal aspect of the dorsal premotor area (F2c), second‐order neuron labeling occurred in the internal segment of the globus pallidus (GPi) and the substantia nigra pars reticulata (SNr). Labeled GPi neurons were found in the caudoventral portion after F2c injection, and in the dorsal portion at the rostrocaudal middle level after F2r injection. In the SNr, F2c and F2r injections led to labeling in the caudal or rostral part, respectively. Subsequently, third‐order neuron labeling was observed in the external segment of the globus pallidus (GPe), the subthalamic nucleus (STN), and the striatum. After F2c injection, labeled neurons were observed over a broad territory in the GPe, whereas after F2r injection, labeled neurons tended to be restricted to the rostral and dorsal portions. In the STN, F2c injection resulted in extensive labeling over the nucleus, whereas F2r injection resulted in labeling in the ventral portion only. After both F2r and F2c injections, labeled neurons in the striatum were widely observed in the striatal cell bridge region and neighboring areas, as well as in the ventral striatum. The present results revealed that the origins of multisynaptic projections to F2c and F2r in the BG are segregated in the output stations of the BG, whereas intermingling rather than segregation is evident with respect to their input station.
The Journal of Neuroscience | 2011
Yosuke Saga; Michiyo Iba; Jun Tanji; Eiji Hoshi
The temporal structuring of multiple events is essential for the purposeful regulation of behavior. We investigated the role of the lateral prefrontal cortex (LPFC) in transforming external signals of multiple sensory modalities into information suitable for monitoring successive events across behavioral phases until an intended action is prompted and then initiated. We trained monkeys to receive a succession of 1 s visual, auditory, or tactile sensory signals separated by variable intervals and to then release a key as soon as the fourth signal appeared. Thus, the animals had to monitor and update information about the progress of the task upon receiving each signal preceding the key release in response to the fourth signal. We found that the initial, short-latency responses of LPFC neurons reflected primarily the sensory modality, rather than the phase or progress of the task. However, a task phase-selective response developed within 500 ms of signal reception, and information about the task phase was maintained throughout the presentation of successive cues. The task phase-selective activity was updated with the appearance of each cue until the planned action was initiated. The phase-selective activity of individual neurons reflected not merely a particular phase of the task but also multiple successive phases. Furthermore, we found combined representations of task phase and sensory modality in the activity of individual LPFC neurons. These properties suggest how information representing multiple phases of behavioral events develops in the LPFC to provide a basis for the temporal regulation of behavior.
European Journal of Neuroscience | 2017
Yosuke Saga; Yoshihisa Nakayama; Kenichi Inoue; Tomoko Yamagata; Masashi Hashimoto; Léon Tremblay; Masahiko Takada; Eiji Hoshi
The thalamic reticular nucleus (TRN) collects inputs from the cerebral cortex and thalamus and, in turn, sends inhibitory outputs to the thalamic relay nuclei. This unique connectivity suggests that the TRN plays a pivotal role in regulating information flow through the thalamus. Here, we analyzed the roles of TRN neurons in visually guided reaching movements. We first used retrograde transneuronal labeling with rabies virus, and showed that the rostro‐dorsal sector of the TRN (TRNrd) projected disynaptically to the ventral premotor cortex (PMv). In other experiments, we recorded neurons from the TRNrd or PMv while monkeys performed a visuomotor task. We found that neurons in the TRNrd and PMv showed visual‐, set‐, and movement‐related activity modulation. These results indicate that the TRNrd, as well as the PMv, is involved in the reception of visual signals and in the preparation and execution of reaching movements. The fraction of neurons that were non‐selective for the location of visual signals or the direction of reaching movements was greater in the TRNrd than in the PMv. Furthermore, the fraction of neurons whose activity increased from the baseline was greater in the TRNrd than in the PMv. The timing of activity modulation of visual‐related and movement‐related neurons was similar in TRNrd and PMv neurons. Overall, our data suggest that TRNrd neurons provide motor thalamic nuclei with inhibitory inputs that are predominantly devoid of spatial selectivity, and that these signals modulate how these nuclei engage in both sensory processing and motor output during visually guided reaching behavior.
Neuroscience Research | 2010
Eiji Hoshi; Yosuke Saga; Daisuke Takahara; Yoshihiro Hirata; Kenichi Inoue; Shigehiro Miyachi; Atsushi Nambu; Jun Tanji; Masahiko Takada
P2-g12 Multisynaptic inputs from the basal ganglia (BG) to rostrocaudally distinct sectors of the dorsal premotor cortex (PMd) in macaques Eiji Hoshi 1 , Yosuke Saga 1, Daisuke Takahara 2,3,4, Yoshihiro Hirata 2,3, Kenichi Inoue 2,3, Shigehiro Miyachi 5, Atsushi Nambu 4, Jun Tanji 1, Masahiko Takada 2,3 1 Tamagawa Univ Brain Sci Inst 2 Dept System Neurosci, Tokyo Metropolitan Inst for Neurosci 3 Systems Neurosci Sect, Primate Res Inst, Kyoto Univ 4 Div System Neurophysiol, National Inst for Physiological Sci 5 Cognitive Neurosci Sect, Primate Res Inst, Kyoto Univ
Neuroscience Research | 2011
Yosuke Saga; Michiyo Iba; Jun Tanji; Eiji Hoshi
Brain and nerve | 2011
Eiji Hoshi; Yoshihisa Nakayama; Tomoko Yamagata; Yosuke Saga; Masashi Hashimoto; Nariko Arimura; Jun Tanji
Neuroscience Research | 2010
Yosuke Saga; Michiyo Iba; Eiji Hoshi; Jun Tanji
Neuroscience Research | 2010
Masashi Hashimoto; Yosuke Saga; Léon Tremblay; Jun Tanji; Eiji Hoshi
Neuroscience Research | 2010
Nariko Arimura; Yoshihisa Nakayama; Tomoko Yamagata; Yosuke Saga; Jun Tanji; Eiji Hoshi
Neuroscience Research | 2009
Eiji Hoshi; Yosuke Saga; Daisuke Takahara; Yoshihiro Hirata; Kenichi Inoue; Shigehiro Miyachi; Jun Tanji; Masahiko Takada