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Sakagami, M.

Publications and source records attributed to Sakagami, M..

3 recordsLinked to original sources

Neurofeedback of prefrontal unit activity during working memory in the macaque

Techniques utilizing neurofeedback, a form of biofeedback using neural signals from the brain, have been applied lately to higher association areas such as the lateral prefrontal cortex (LPFC); however, it remains unexplored how well neurofeedback using unit activity in the LPFC modulates its working memory-related activity and performance. To address this issue, we provided neurofeedback of LPFC unit activity during a delay period to two monkeys while they performed a delayed matching-to-paired-sample task. In the task, neurofeedback allowed the animals to shorten the delay length by increasing delay activity and make an earlier choice. Neurofeedback significantly increased delay activity in two-thirds of task-related neurons. Notably, in 16% of these neurons, a preference for delay activity and performance dependent on the stimulus emerged. Although neurofeedback decreased performance primarily due to choice errors, the disassociation of neurofeedback linkage rescued performance. Further, the neuronal activity of simultaneously recorded neurons without neurofeedback linkage suggests that neurofeedback reconfigured the net activity of the LPFC to adapt to new situations. These findings indicate that LPFC neurons can dynamically multiplex different types of information to adapt to environmental changes. Thus, we demonstrated the significant potential of neurofeedback using unit activity to investigate information processing in the brain.

neuroscience↗

Only cortical prediction error signals are involved in visual learning, despite availability of subcortical prediction error signals

Both the midbrain systems, encompassing the ventral striatum (VS), and the cortical systems, including the dorsal anterior cingulate cortex (dACC), play roles in reinforcing and enhancing learning. However, the specific contributions of signals from these regions in learning remains unclear. To investigate this, we examined how VS and dACC are involved in visual perceptual learning (VPL) through an orientation discrimination task. In the primary experiment, subjects fasted for 5 hours before each of 14 days of training sessions and 3 days of test sessions. Subjects were rewarded with water for accurate trial responses. During the test sessions, BOLD signals were recorded from regions including VS and dACC. Although BOLD signals in both areas were associated with positive and negative RPEs, only those in dACC associated with negative RPE showed a significant correlation with performance improvement. Additionally, no significant correlation was observed between BOLD signals associated with RPEs in VS and dACC. These results suggest that although signals associated with positive and negative RPEs from both midbrain and cortical systems are readily accessible, only RPE signals in the prefrontal system, generated without linking to RPE signals in VS, are utilized for the enhancement of VPL.

neuroscience↗

Gsx2 is involved in specification of neurons in the inferior olivary nuclei from Ptf1a-expressing neuronal progenitors in zebrafish

Neurons in the inferior olivary nuclei (IO neurons) send climbing fibers to Purkinje cells to elicit functions of the cerebellum. IO neurons and Purkinje cells are derived from neural progenitors expressing the proneural gene ptf1a. In this study, we found that the homeobox gene gsx2 was co-expressed with ptf1a in IO progenitors in zebrafish. Both gsx2 and ptf1a zebrafish mutants showed a strong reduction or loss of IO neurons. The expression of ptf1a was not affected in gsx2 mutants and vice versa. In IO progenitors, the ptf1a mutation increased apoptosis whereas the gsx2 mutation did not, suggesting that ptf1a and gsx2 are independently regulated and have distinct roles. The fibroblast growth factors (Fgf) 3/8a and retinoic acid signals negatively and positively, respectively, regulated gsx2 expression and thereby the development of IO neurons. mafba and hox genes are at least partly involved in the Fgf- and retinoic acid-dependent regulation of IO neuronal development. Our results indicate that gsx2 mediates the rostro-caudal positional signals to specify the identity of IO neurons from ptf1a-expressing neural progenitors. SummaryThe homeobox gene gsx2 mediates rostro-caudal positional signaling to specify the identify of neurons in the inferior olivary nuclei from neural progenitors expressing the proneural gene ptf1a.

developmental biology↗