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Biomedical subjects

Masayuki Nakao

Publications and source records attributed to Masayuki Nakao.

12 recordsLinked to original sources

Liquid filling method for nanofluidic channels utilizing the high solubility of CO2.

We developed a fabrication method and a liquid filling method for a nano chemical reactor that used Y-shaped nanochannels specially designed for mixing and reacting. In order to reduce the pressure loss and to utilize the characteristics of the nanochannel, inlet microchannels were fabricated just beside the nanochannels. We investigated an initial liquid filling method into the nanochannels that ensured there were no air bubbles that could cause a flow stack due to the capillary pressure. In our method, the micro- and nanochannels were filled with carbon dioxide and any remaining air during the initial liquid introduction was dissolved utilizing the high solubility of carbon dioxide. We propose that chemical reactions in nanospaces can be realized by utilizing these fabrication and liquid introduction techniques.

Journal Article↗

Interfield differences in intensity and frequency representation of evoked potentials in rat auditory cortex.

Existing studies have demonstrated interfield differences in functional organizations and neuronal responsive properties at a single neuron level in the auditory cortex, suggesting complicated encoding of sound frequency and intensity. The objective of present work is, by characterizing cortical auditory evoked potentials (AEPs), to bridge neural characteristics between a single neuron and field levels and to identify the interfield differences in the auditory cortex specifically in terms of spatial representation, which will be useful in guiding future unit studies. The AEP mapping found that each of auditory fields, which could be identified by a different tonotopic representation, showed interfield differences in an intensity-dependent spatial change, amplitude, latency, and amplitude-SPL (sound pressure level) function. These results also showed that many aspects of cortical representation were based on the cochlear properties, yet some were inconsistent. The intensity-dependent shift of activation in AI paralleled the tonotopic axis, which was similar to the place code in cochlea, while the shift in AAF and VAF did not parallel. Nevertheless, the amplitude-SPL function suggested that an underlying mechanism of all these shifts can be a compressive nonlinearity to CF tone, which is possibly formed in the cochlea and still preserved in the cortex. These results suggest that each field modifies the representation to handle a different aspect of sound information, which can be better analyzed than the cochlear representation.

Acoustic Stimulation↗

Alaryngeal speech aid using an intra-oral electrolarynx and a miniature fingertip switch.

We developed and evaluated an intra-oral electrolaryngeal speech aid system for those who could not acquire common alaryngeal speech or for early post-surgery speech rehabilitation. Our system consisted of a denture-base intra-oral vibrator, a wireless miniature fingertip switch and a controller. To produce natural speech, the fingertip switch produced binary commands of voicing and accent and the controller implemented the pitch generation model using the commands. We first estimated the intelligibility of consonant-vowel syllables produced by our system. We then obtained the feedback about the system from the Japanese users on the basis of their daily life use, and evaluated the possibility and acceptability as an alaryngeal speech aid. Although the users were less satisfied at the intra-oral electrolarynx, the intelligibility of the intra-oral electrolarygeal speech was comparable to that of transcervical electrolaryngeal speech, and most of them were willing to employ it if they lost their current electrolaryngeal speech. According to the feedbacks from the users, a completely wire-free system and less eye-catching designs would make the prosthesis more acceptable. These results placed the intra-oral electrolarynx as a useful option of alaryngeal speech aids and encouraged the further development of the intra-oral electrolarynx.

Aged↗

Spatial and temporal strategy to analyze steady-state sound intensity in cortex.

Prevailing studies of auditory systems pay most attention to the dynamic temporal changes of sound intensity, but poorly enlighten the encoding of steady-state aspects. Using tone bursts as test stimuli, we epipially map auditory evoked potentials over the rat auditory cortex and investigate how the cortex represents the dynamic and steady states. Our results demonstrate that all of the auditory fields investigated potentially have at least two strategies to represent the two states; a temporal combination of early and late components of the potentials, and a spatial combination of an arbitrary component. In addition, the optimal combination that can distinguish between the two states differs across auditory fields, suggesting robust analyses of sound intensity in the auditory cortex.

Acoustic Stimulation↗

Easy-to-prepare assembly array of Tungsten microelectrodes.

This paper provides a detailed process flow for fabricating an easy-to-prepare, inexpensive, dense array of tungsten microelectrodes. We designed the process flow to minimize routine tasks by separating an initial preparation of a master mold from a routine preparation of substrate replication, array assembly and tip processing. Sandblast processing first produced a glass mold with a pattern of a series of protruding lines at a requested interval of a few hundred micrometers. Copying the groove pattern onto polystyrene mass-produced a replica substrate. Tungsten probes were then aligned on the substrate, and the tips of probes were finely processed in the block.

Action Potentials↗

Accessing ampli-tonotopic organization of rat auditory cortex by microstimulation of cochlear nucleus.

Auditory brainstem implants (ABI) that electrically stimulate the surface of cochlear nucleus have been clinically used for the rehabilitation of deaf patients with bilateral vestibular schwannomas. The change of pitch perception with an active electrode location is not as clear in ABIs as in cochlear implants, a factor which might play a role in poorer speech performance in ABIs. The objective of present work was to develop an animal ABI model that could provide physiological data for future ABI development and optimization. The experimental system included a penetrating microelectrode array for microstimulation of the cochlear nucleus and a surface microelectrode array for mapping evoked potentials over the auditory cortex. We first obtained tone-evoked cortical activation patterns, which represented a place code of the frequency and intensity of test tones, i.e., the ampli-tonotopic organization, and compared the patterns with those evoked by cochlear nuclear microstimulation. Our experimental results demonstrated that microstimulation of both the dorsal and ventral cochlear nucleus (DCN and VCN) could access the cortical ampli-tonotopic organization as acoustic stimuli did. We also found that the cortical dynamic range was wider for the DCN than VCN stimulation and for the low-frequency than for the high-frequency pathway. The present results have great implications for improved ABI performance.

Action Potentials↗

Distributed representation of sound intensity in the rat auditory cortex.

We epipially mapped tone-burst-evoked potentials over the rat auditory cortex, and investigated the representation of intensity information. The experiments were designed to elucidate how the auditory cortex represents a steady-state plateau sound pressure level (SPL) and dynamic onset temporal structure, i.e., the rate of pressure change (in Pa/s), and how the representations differ across the auditory fields. The anterior and ventral fields have spatial axes of the rate of pressure change. Characteristic frequency (CF) locations mainly handle the dynamic state, while off-CF locations have the potential to code the steady state. Each field represents the intensity information differently, particularly at the off-CF locations. These results suggest that intensity information is distributed in various aspects in the multiple auditory fields.

Acoustic Stimulation↗

Cortical mapping of auditory-evoked offset responses in rats.

We characterized the auditory-evoked offset responses of the rat auditory cortex by multiple-site surface microelectrode recording. Tone bursts served as test stimuli. Offset responses did not appear tonotopically, but at the fringe of tonotopic onset distributions. Offset amplitude was significantly sensitive to sound intensity, fall time at tone termination, and duration. These results suggest that offset responses are associated with inhibitory responses surrounding excitatory onset responses, and offset responses become large when inhibition becomes strong and long or terminates synchronously. Thus, the rebound after the inhibition in the presence of a stimulus is likely to be a major cause of offset responses in the auditory cortex.

Acoustic Stimulation↗

Cell culture in a closed nano-space.

The minimum size of a closed nano-space in which cells can survive was determined using 4-nl nanowells. One or two cells could divide in the nanowell. Our results suggest that the cell division activity in the nano-space is determined by the conflict between intercellular effects and consumption of substrates.

Journal Article↗

Microelectrode array on folding polyimide ribbon for epidural mapping of functional evoked potentials.

This paper describes a flexible polyimide microelectrode ribbon with a bending structure for epidural recording. Bending the ribbon establishes good electro-mechanical contact of the electrodes to the cortex. Impedance spectroscopy and noise measurements in vitro were used to characterize the electrodes. Our in vivo experiments then successfully achieved synchronized neuronal activity and evoked potential patterns useful for understanding brain function and for finding cortical function.

Action Potentials↗

Nanochannels on a fused-silica microchip and liquid properties investigation by time-resolved fluorescence measurements.

We have fabricated nanometer-sized channels, demonstrated a technique for the introduction of liquid into the channels, and carried out time-resolved fluorescence measurements of aqueous solutions. In this study, 330-nm- and 850-nm-sized channels were fabricated on fused-silica substrates by fast atom beam etching and hydrofluoric acid bonding methods. A liquid introduction method utilizing capillary action was demonstrated. The liquid introduction was observed under an optical microscope, and the liquid velocity during the introduction was analyzed by surface energy and macroscale hydrodynamics. The liquid velocity due to capillary action in the nanometer-sized channel seemed more than four times slower than the estimation. Then, aqueous solutions of rhodamine 6G (R6G), sulforhodamine 101 (SR101), and rhodamine B (RB) in the channels were measured by time-resolved fluorescence spectroscopy; spectra of the same solution in a 250-microm-sized channel were also measured as a reference for the macrospace. Although the fluorescence spectra in the 330-nm-, 850-nm- and 250-microm-sized channels agreed with one another, the fluorescent decays in the nanometer-sized channels were faster for R6G and SR101 and slower for RB than the respective decays in the 250-microm-sized channels. The results suggested the solutions had lower dielectric constants and higher viscosities in the nanometer-sized channels.

Journal Article↗