Xiping Zhan, Ph.D.

Xiping Zhan, Ph.D.

Howard University
Dopaminergic activity in modulation of noise-induced tinnitus

Tinnitus is a major challenge for public health because it is a condition that is associated with hearing loss and can contribute to debilitating emotional stress, anxiety, and mental fatigue. Dr. Zhan’s interest is focused on the mechanisms that generate tinnitus and modulate tinnitus associated anxiety and depression using an animal model. His studies focus on dopaminergic activity in the limbic midbrain. Dopamine and its receptors play an important role in human mood behavior. Recently, dopamine has been suggested to be involved in tinnitus. Dr. Zhan’s research is designed to find out how dopamine neurons are communicating with other neurons to contribute to tinnitus generation. In addition, he also investigates how the functions of dopamine cells are modified during the development of tinnitus following noise exposures. These studies will shed light on the cellular mechanisms of tinnitus and offer a novel avenue for drug therapy.

Ning Zhou, Ph.D.

Ning Zhou, Ph.D.

East Carolina University
Place specificity of electrical stimulation with a cochlear implant and its relationship to neural survival and speech recognition

Modern cochlear implants code a speech signal by dividing it into spectral channels and modulating trains of biphasic electrical pulses with the low-frequency temporal envelope from each channel. Perception with a cochlear implant therefore is dependent on two factors: the acuity of processing the low frequency amplitude modulations and the place specificity of excitation. Cochlear implant users have demonstrated amplitude modulation detection similar to that found in normal hearing ears with larger individual variability, nonetheless the challenge of the prosthesis lies with the poor place specificity. Ideally, the output of an electrode should target a specific population of nerve fibers. However spread of excitation is often large, leading to neural interactions between channels. The first aim of the research is to investigate whether the underlying cause of channel interaction is the status of neural survival near the stimulation sites. The hypothesis is that excitation is more likely to spread further from a stimulation site in the cochlea when the density of surviving spiral ganglion cells is sparse. Neural status of a stimulation site will be estimated using a non-invasive psychophysical measure that correlates with the count of spiral ganglion cells in implanted animals. Place specificity of excitation will be measured by a psychophysical forward-masking procedure that is widely used to assess spatial tuning in electrical hearing. The second aim of the research is to examine the effects of place specificity on speech perception that requires mainly the spectral cues. The rationale is that poor place specificity would cause a reduction in spectral resolution or smearing of spectral speech cues. Proposed speech recognition tasks that demand good spatial tuning are perception of sine-wave speech, also known as the spectral skeleton of speech, and perception of speech presented in background noises.

Research area: Cochlear Implants

Long-term goal of research: If the proposed hypothesis is correct, that is, poor neural survival predicts poor spatial tuning, we will seek to ask the question whether the temporal processing acuity of the activated neurons at the site with low cell density would also be compromised. Once the relationship between temporal and spatial acuity is determined, we will examine the relative importance of the temporal and spatial acuity for speech recognition. The two acuities might not be equally important, or that they might be contributing to different aspects of speech recognition. With this information, the long term goal is to optimize implant user’s speech processing MAPs by strengthening the perception acuity that is the most important for speech recognition in the ear.

Junhuang Zou, Ph.D.

Junhuang Zou, Ph.D.

University of Utah
Understanding the function of PDZD7 in hair cells

Usher syndrome is a devastating genetic disease affecting both hearing and vision. It is the leading genetic cause of combined deafness and blindness in the world. Usher syndrome is clinically and genetically heterozygous. It is classified into three clinical types according to the severity of hearing and vestibular symptoms. Zou's studies focus on type 2, which is the dominant form of Usher syndrome and characterized by congenital moderate degree of hearing loss, normal vestibular function, and retinitis pigmentosa. PDZD7 was recently reported to exacerbate the symptoms and contribute the digenic form of Usher syndrome type 2 when patients carry heterozygous PDZD7 mutations. Zou has successfully generated a Pdzd7 knockout mouse. Using this animal model, Zou plans to investigate the function of PDZD7 during hair bundle development in the cochlea. This study will be significant for the future diagnosis and treatments for Usher syndrome type 2.