UMI  
ProQuest® Dissertations & Theses
The world's most comprehensive collection of dissertations and theses. Learn more...
ProQuest  
 
 
Alteration of susceptibility to noise-induced hearing loss through interruption of sympathetic inputs to the cochlea
by Bielefeld, Eric, Ph.D., STATE UNIVERSITY OF NEW YORK AT BUFFALO, 2005, 184 pages; 3185279
 

Abstract:

In 1966, sympathetic fibers were identified in the cochlea, terminating on the cochlear artery and near the auditory nerve fibers at the level of the habenula perforata (Spoendlin and Lichtensteiger, 1966). The cochlear sympathetic fibers originate in the stellate ganglion (SG) and the superior cervical ganglion (SCG). Both sets of fibers have a demonstrated effect on cochlear blood flow (CBF) (Laurikainen et al., 1993, 1994, 1997; Ren et al., 1993). The SCG fibers have been implicated in modulation of susceptibility to noise-induced hearing loss (NIHL) (Borg, 1982; Hildesheimer et al., 1991; Horner et al., 2001; Hildesheimer et al., 2002). Ablation of the SCG generally leads to protection from NIHL, but the previous studies do not separate the effects of SCG ablation on temporary and permanent threshold shift (TTS and PTS), and there is also some question about whether the effect is unilateral or bilateral.

In the current study, we explore the effects of unilateral and bilateral SCG ablation on threshold shift from noise exposure, as measured with inferior colliculus (IC) evoked potentials, distortion product otoacoustic emissions (DPOAE), and outer hair cell (OHC) loss. SCGs were isolated at the level of the bifurcation of the carotid artery and removed unilaterally in 15 chinchillas. Another 8 chinchillas underwent bilateral ablation. 20 animals were employed as sham controls. Each animal was implanted with IC electrodes and exposed to an octave band noise centered at 4 kHz for one hour at 110 dB SPL. Hearing thresholds and DPOAE input/output functions were measured at six hours, one day, three days, one week, and three weeks after the noise. After the three-week test, animals were sacrificed and OHCs were counted for cochleograms. Results showed improved recovery of DPOAE amplitudes after noise exposure in ears that underwent SCGectomy, as well as lower evoked potential threshold shifts relative to sham controls. Effects of SCGectomy on OHC loss were small. Results of the study suggest that sympathetic fibers do exert some influence on susceptibility to noise, but the influence may not be a major one.

 
Advisor: Henderson, Donald
School: STATE UNIVERSITY OF NEW YORK AT BUFFALO
Source: DAI-B 66/08, p. 4144, Feb 2006
Source Type: Ph.D.
Subjects: Audiology
Publication Number: 3185279
     
Adobe PDF Access the complete dissertation:
 

» Find an electronic copy at your library.
  Use the link below to access a full citation record of this graduate work:
  http://gateway.proquest.com/openurl%3furl_ver=Z39.88-2004%26res_dat=xri:pqdiss%26rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation%26rft_dat=xri:pqdiss:3185279
  If your library subscribes to the ProQuest Dissertations & Theses (PQDT) database, you may be entitled to a free electronic version of this graduate work. If not, you will have the option to purchase one, and access a 24 page preview for free (if available).

 
 
 

About ProQuest Dissertations & Theses
With over 2.3 million records, the ProQuest Dissertations & Theses (PQDT) database is the most comprehensive collection of dissertations and theses in the world. It is the database of record for graduate research.

The database includes citations of graduate works ranging from the first U.S. dissertation, accepted in 1861, to those accepted as recently as last semester. Of the 2.3 million graduate works included in the database, ProQuest offers more than 1.9 million in full text formats. Of those, over 860,000 are available in PDF format. More than 60,000 dissertations and theses are added to the database each year.

If you have questions, please feel free to visit the ProQuest Web site - http://www.il.proquest.com - or call ProQuest Hotline Customer Support at 1-800-521-3042.



Copyright © 2007 ProQuest. All rights reserved. Terms and Conditions

ProQuest