Biomedical subjects

Rei Yamada

Publications and source records attributed to Rei Yamada.

3 recordsLinked to original sources

PubMed2005

Hyperpolarization-activated cyclic nucleotide-gated cation channels regulate auditory coincidence detection in nucleus laminaris of the chick.

Coincidence detection of bilateral acoustic signals in nucleus laminaris (NL) is the first step in azimuthal sound source localization in birds. Here, we demonstrate graded expression of hyperpolarization-activated cyclic nucleotide-gated (HCN) cation channels along the tonotopic axis of NL and its role in the regulation of coincidence detection. Expression of HCN1 and HCN2, but not HCN3 or HCN4, was detected in NL. Based on measurement of both subtype mRNA and protein, HCN1 varied along the tonotopic axis and was minimal in high-characteristic frequency (CF) neurons. In contrast, HCN2 was evenly distributed. The resting conductance was larger and the steady-state activation curve of Ih was more positive in neurons of middle to low CF than those of high CF, consistent with the predominance of HCN1 channels in these neurons. Application of 8-Br-cAMP or noradrenaline generated a depolarizing shift of the Ih voltage activation curve. This shift was larger in neurons of high CF than in those of middle CF. The shift in the activation voltage of Ih depolarized the resting membrane, accelerated the EPSP time course, and significantly improved the coincidence detection in neurons of high CF, suggesting that Ih may improve the localization of sound sources.

Animals↗

PubMed2005

Tonotopic specialization of auditory coincidence detection in nucleus laminaris of the chick.

The interaural time difference (ITD) is a cue for localizing a sound source along the horizontal plane and is first determined in the nucleus laminaris (NL) in birds. Neurons in NL are tonotopically organized, such that ITDs are processed separately at each characteristic frequency (CF). Here, we investigated the excitability and coincidence detection of neurons along the tonotopic axis in NL, using a chick brainstem slice preparation. Systematic changes with CF were observed in morphological and electrophysiological properties of NL neurons. These properties included the length of dendrites, the input capacitance, the conductance of hyperpolarization-activated current, and the EPSC time course. In contrast to these gradients, the conductance of low-threshold K+ current and the expression of Kv1.2 channel protein were maximal in the central (middle-CF) region of NL. As a result, the middle-CF neuron had the smallest input resistance and membrane time constant, and consequently the fastest EPSP, and exhibited the most accurate coincidence detection. The specialization of middle-CF neurons as coincidence detectors may account for the high resolution of sound-source localization in the middle-frequency range observed in avians.

Action Potentials↗

PubMed2003

Evaluation of the limiting acuity of coincidence detection in nucleus laminaris of the chicken.

The localization of sounds requires the detection of very brief inter-aural time differences (ITDs). In birds, ITDs are first encoded in neurons of the nucleus laminaris (NL) through the precise coincidence of binaural synaptic inputs. We examined the effects of temperature on acuity of coincidence detection in chick NL, by utilizing whole-cell and cell-attached recording techniques in brain slices while applying electrical stimuli bilaterally to axonal projections from the nucleus magnocellularis to NL. The precision of coincidence detection was measured as a time window, corresponding to the time interval that gave the half-maximum spiking probability. Acuity improved with the elevation of recording temperature, and at 40 degrees C, the avian body temperature, the time window was 0.38 ms. Although all synaptic events were briefer at higher temperature, the duration of EPSPs were equivalent to or faster than that of EPSCs at 40 degrees C. Activation of low-threshold K+ currents by a slight membrane depolarization during an EPSP was responsible for this EPSP acceleration. EPSPs were prolonged following inhibition of low-threshold K+ currents by dendrotoxin (40 nM) or hyperpolarization-activated cation currents by Cs+ (3 mM). The EPSP time course had a strong positive correlation with the sharpness of coincidence detection. The limiting value of the time window (0.16 ms), calculated from the estimated EPSP time course, was narrow enough to explain the acuity of ITD detection at NL in vivo.

Animals↗