Blood circulation disturbances contribute to the hearing loss in loud-sound induced trauma, aging, Meniere's disease, ototoxic drugs and some forms of sudden deafness. Knowledge of inner ear vascular physiology is fundamental to understanding and treating these hearing conditions, but the field remains poorly explored. The long-term goal of this lab is to determine the common and unique patho-physiological mechanisms of cochlear vessels, the key neurohumoral messengers, receptors and channels responsible for cochlear blood flow regulation, and to discover drugs for prevention and treatment of these hearing losses. Our previous studies have found that the cochlear spiral modiolar artery (SMA) has unique vascular tone control mechanisms in resting membrane potential (RP) regulation and neuromuscular transmission. Based on these findings, this proposal sets the following aims: 1) to determine the mechanism and significance that underlie the bi-modal RP distribution of the SMA cells and the mechanism by which ischemia/reperfusion causes the change of the RP distribution and vasotone response;2) to determine the ion channel(s) and receptor type(s) that mediate the actions of the candidate neurotransmitters (e.g., norepinephrine, acetylcholine, CGRP);3) to identify the role of candidate neurotransmitters in intrinsic neuromuscular transmission in the SMA. These goals will be achieved through experiments using conventional and whole-cell current- and voltage-clamp recording methods on the in vitro vascular smooth muscle cells (VSMC), plus multiple approaches such as computational modeling, vaso-diameter tracking, nitric oxide production-monitoring, immunocytochemistry, RT-PCR and Western blot analyses. With these studies, we expect to find that the Key channel protein, Kir, co-plays with other persistent membrane currents, such as KATP and Na+K+pump currents, to generate the bimodal RP and thus to achieve a high autoregulation capacity of cochlear blood flow. We also anticipate that ischemia/reperfusion treatment will cause up-regulation of nitric oxide production, KATP and Kir expression, and thus cause the RP population shift and the vascular responsiveness change. The novel neuromuscular transmission and various drug effects will be characterized. The knowledge obtained will improve our understanding of how cochlear blood flow is regulated and what are the key factors causing cochlear circulation-deficiency, thus contributing to better prevention and treatment of the circulation-implicated hearing loss, and even the heart attack &stroke. The knowledge obtained should improve our understanding of how cochlear blood flow is uniquely regulated, thus contributing to understanding of circulation-related hearing losses and leading to prevention and treatment of these hearing conditions. The acquired knowledge should also be of significance in broad areas of cardiovascular physiology, and cardiovascular disease pathophysiology.

Public Health Relevance

The knowledge obtained should improve our understanding of how cochlear blood flow is uniquely regulated, thus contributing to understanding of circulation-related hearing losses and leading to prevention and treatment of these hearing conditions. The acquired knowledge should also be of significance in broad areas of cardiovascular physiology, and cadiovascular disease pathophysiology.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC004716-07
Application #
7790796
Study Section
Auditory System Study Section (AUD)
Program Officer
Donahue, Amy
Project Start
2000-12-01
Project End
2014-03-31
Budget Start
2010-04-01
Budget End
2011-03-31
Support Year
7
Fiscal Year
2010
Total Cost
$323,978
Indirect Cost
Name
Oregon Health and Science University
Department
Otolaryngology
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
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