The cochlea receives its main blood supply from the basilar artery, via the anterior inferior cerebellar artery and the spiral modiolar artery. It is of clinical importance to understand the mechanisms that regulate cochlear blood flow, since many hearing disorders, such as sensorineural hearing loss, acute acoustic trauma, noise-induced hearing loss, tinnitus, Meniere's disease and presbyacusis may be caused or aggravated by localized vasospasms that pathologically limit cochlear blood flow and cause transient ischemic events. Calcium is the major focus of this proposal since it is obligatory for vasoconstrictions. The cytosolic Calcium concentration in vascular smooth muscle cells is tightly controlled and effectively compartmentalized into pools that mediate vasoconstriction and pools that mediate vasodilation. Calcium that mediates vasoconstriction is commonly released as Calcium waves and calcium that mediates vasodilations is commonly released as Calcium sparks. In general, the cytosolic Calcium concentration is controlled via export/import across the plasma membrane and in and out of cytosolic Calcium stores. The extracellular Calcium concentration may not only serve as a simple reservoir for Calcium but constitute an important paracrine messenger that has so far received little attention. For this proposal we have targeted two major areas focused on Calcium as it relates to the cellular regulation of cochlear blood flow. Most experiments will be performed using an isolated in vitro superfused preparation of the spiral modiolar artery. Vascular diameter will be measured by videomicroscopy and cytosolic Calcium by confocal microfluorometry. The presence of receptors and ion channels will be determined by a combination of a pharmacological approach using functional assays, a molecular biological approach and a protein biochemical approach.
Under Specific Aim 1, we will determine whether different modes of Calcium release from cytosolic stores cause vasodilations and constrictions, respectively.
Under Specific Aim 2 we will determine how smooth muscle cells sense the extracellular Calcium concentration. Completion of these Specific Aims will greatly enhance our understanding of the cellular mechanisms of cochlear blood flow regulation, which is a necessary prerequisite for the rational design of pharmacological interventions needed to combat a multitude of hearing disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC004280-10
Application #
8209240
Study Section
Auditory System Study Section (AUD)
Program Officer
Cyr, Janet
Project Start
1999-04-01
Project End
2014-12-31
Budget Start
2012-01-01
Budget End
2014-12-31
Support Year
10
Fiscal Year
2012
Total Cost
$293,454
Indirect Cost
$92,458
Name
Kansas State University
Department
Anatomy/Cell Biology
Type
Schools of Veterinary Medicine
DUNS #
929773554
City
Manhattan
State
KS
Country
United States
Zip Code
66506
Reimann, Katrin; Krishnamoorthy, Gayathri; Wangemann, Philine (2013) NOS inhibition enhances myogenic tone by increasing rho-kinase mediated Ca2+ sensitivity in the male but not the female gerbil spiral modiolar artery. PLoS One 8:e53655
Krishnamoorthy, Gayathri; Regehr, Keil; Berge, Samantha et al. (2011) Calcium sparks in the intact gerbil spiral modiolar artery. BMC Physiol 11:15
Reimann, Katrin; Krishnamoorthy, Gayathri; Wier, Withrow Gil et al. (2011) Gender differences in myogenic regulation along the vascular tree of the gerbil cochlea. PLoS One 6:e25659
Scherer, Elias Q; Yang, Jingli; Canis, Martin et al. (2010) Tumor necrosis factor-ýý enhances microvascular tone and reduces blood flow in the cochlea via enhanced sphingosine-1-phosphate signaling. Stroke 41:2618-24
Wangemann, Philine; Wonneberger, Kai (2005) Neurogenic regulation of cochlear blood flow occurs along the basilar artery, the anterior inferior cerebellar artery and at branch points of the spiral modiolar artery. Hear Res 209:91-6
Wangemann, Philine (2002) Cochlear blood flow regulation. Adv Otorhinolaryngol 59:51-7
Scherer, Elias Q; Wangemann, Philine (2002) ETA receptors in the gerbil spiral modiolar artery. Adv Otorhinolaryngol 59:58-65
Herzog, M; Scherer, E Q; Albrecht, B et al. (2002) CGRP receptors in the gerbil spiral modiolar artery mediate a sustained vasodilation via a transient cAMP-mediated Ca2+-decrease. J Membr Biol 189:225-36
Scherer, Elias Q; Herzog, Michael; Wangemann, Philine (2002) Endothelin-1-induced vasospasms of spiral modiolar artery are mediated by rho-kinase-induced Ca(2+) sensitization of contractile apparatus and reversed by calcitonin gene-related Peptide. Stroke 33:2965-71
Scherer, E Q; Wonneberger, K; Wangemann, P (2001) Differential desensitization of Ca2+ mobilization and vasoconstriction by ET(A) receptors in the gerbil spiral modiolar artery. J Membr Biol 182:183-91

Showing the most recent 10 out of 11 publications