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Non-insulin-dependent diabetic microangiopathy in the inner ear

Published online by Cambridge University Press:  29 June 2007

Chapman T. McQueen*
Affiliation:
Division of Otolaryngology/Head and Neck Surgery, University of North Carolina School of Medicine, Chapel Hill, North Carolina
Andrew Baxter
Affiliation:
Division of Otolaryngology/Head and Neck Surgery, University of North Carolina School of Medicine, Chapel Hill, North Carolina
Timothy L. Smith
Affiliation:
Division of Otolaryngology/Head and Neck Surgery, University of North Carolina School of Medicine, Chapel Hill, North Carolina
Eileen Raynor
Affiliation:
Division of Otolaryngology/Head and Neck Surgery, University of North Carolina School of Medicine, Chapel Hill, North Carolina
Sang Min Yoon
Affiliation:
Department of Otolaryngology, Catholic University Medical College, St. Vincent Hospital, Suwon, Korea.
Jiri Prazma
Affiliation:
Division of Otolaryngology/Head and Neck Surgery, University of North Carolina School of Medicine, Chapel Hill, North Carolina
Harold C. Pillsbury III
Affiliation:
Division of Otolaryngology/Head and Neck Surgery, University of North Carolina School of Medicine, Chapel Hill, North Carolina
*
Address for correspondence: Chapman T. McQueen, M.D., Division of Otolaryngology/Head & Neck Surgery, 610 Burnett-Womack Bldg., CB# 7070, University of North Carolina School of Medicine, Chapel Hill, NC 27599-7070, USA. Fax: +919-966-7656

Abstract

Hearing loss has long been associated with diabetes mellitus. Microangiopathy, associated with thickening of the basement membranes of small vessels, has been implicated as a major source of multiple system organ disease.

Objective This study was designed to evaluate changes in basement membrane thickness in the inner ear of laboratory animals suffering from non-insulin-dependent diabetes mellitus (NIDDM) with, and without, exposure to moderate intensity noise exposure in an attempt to extrapolate the same disease process in humans.

Design Spontaneously hypertensive-corpulent non-insulin-dependent rats (SHR/N-cp) were selected as a genetic model for the above study. Both lean and obese rats were used in this study. A genetically similar control group of animals (LA/N-cp) were used as controls. These animals express both the lean and obese phenotypes, but they lack the NIDDM gene. Forty-eight animals in each group were sacrificed at the end of the study. The cochleas were dissected and fixed. The basement membrane of the stria vascularis was examined using transmission electron microscopy.

Setting This study was a laboratory-based, standard animal study.

Main outcome This study was designed to show microangiography of the inner ear as related to NIDDM with, and without, obesity and noise exposure.

Results/Conclusions NIDDM alone does not cause statistically significant basement membrane thickening; however, NIDDM in combination with obesity and/or noise exposure did show significant thickening and the combination of all three showed the greatest thickening. NIDDM appeared to be the greatest contributing factor.

Type
Main Articles
Copyright
Copyright © JLO (1984) Limited 1999

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References

Borsuk, J., Lisiecha, H., Majcherska, B. (1956) The audiometric curve in diabetes mellitus. Polskie Archiwum Medycyny Wewnetrznej (Poland) 26: 11591166.Google ScholarPubMed
Dengerink, H., Miller, J., Axelsson, A., Vertes, D., Van Dalfsen, P. (1985) The recovery of vascular changes following brief noise exposure. Acta Otolaryngologica 100: 1925.CrossRefGoogle ScholarPubMed
Gibbin, K. P., Davis, C. G. (1981) A hearing survey in diabetes mellitus. Clinical Otolaryngology 6(5): 345350.CrossRefGoogle ScholarPubMed
Harner, S. G. (1981) Hearing in adult-onset diabetes mellitus. Otolaryngology – Head and Neck Surgery 89(2): 322327.CrossRefGoogle ScholarPubMed
Hawkins, J. E. (1971) The role of vasoconstriction in noiseinduced hearing loss. Annals of Otology, Rhinology and Laryngology 80: 903.CrossRefGoogle Scholar
Hodgson, M. J., Talbott, E. O., Helmkamp, J. C., Kuller, L. H. (1987) Diabetes, noise exposure and hearing loss. Journal of Occupational Medicine 29: 576579.Google ScholarPubMed
Ishii, E. K., Talbott, E. O., Findlay, R. C., D'Antonio, J. A., Kuller, L. H. (1992) Is NIDDM a risk factor for noiseinduced hearing loss in an occupationally noise exposed cohort? Science of Total Environment 127(12): 155165.CrossRefGoogle Scholar
Jordao, A. M. D. (1857) Consideration sur un cas du diabete. Union medicale du Paris 11: 446.Google Scholar
Jorgensen, M. B. (1961) The inner ear in diabetes mellitus. Archives of Otolaryngology – Head and Neck Surgery 74: 3139.CrossRefGoogle ScholarPubMed
Koletsky, S. (1973) Obese spontaneously hypertensive rats – a model for study of atherosclerosis. Experimental Molecular Pathology 19: 5360.CrossRefGoogle Scholar
Koslov, M. T. (1975) Changes of the hearing level in patients with diabetes mellitus. Zhurnal Ushnykh, Nosovykh i Gorlovykh Boleznei (Russian) 1: 3236.Google Scholar
Lonsbury-Martin, B. L., Martin, G. K. (1993) Auditory dysfunction from excessive sound stimulation. In Otolaryngology – Head and Neck Surgery, Ear and Cranial Base (Cummings, C. W., Fredrickson, J. M., Harker, L. A., Krause, C. J., Schuller, D. E. eds.) 2nd Edition. Vol. 4. Mosby-Year Book Inc., St Louis, pp 28852900.Google Scholar
Raynor, E. M., Carrasco, V. N., Prazma, J., Pillsbury, H. C. (1995) An assessment of cochlear hair cell loss in IDDM diabetic and noise-exposed rats. Archives of Otolaryngology – Head and Neck Surgery 121: 452456.CrossRefGoogle ScholarPubMed
Robison, W. G., Kador, P. F., Kinoshita, J. H. (1983) Retinal capillaries: basement membrane thickening by galactosemia prevented with aldose reductase inhibitor. Science 221: 11771179.CrossRefGoogle ScholarPubMed
Rust, L., Prazma, J., Triana, R. J., Michaelis, O. E., Pillsbury, H. C. (1992) Inner ear damage secondary to diabetes mellitus, Part II: changes in aging SHR/N-cp rats. Archives of Otolaryngology – Head and Neck Surgery 118: 397400.CrossRefGoogle Scholar
Smith, T. L., Raynor, E. M., Prazma, J., Buenting, J. E., Pillsbury, H. C. (1995) Insulin dependent diabetic microangiopathy in the inner ear. Laryngoscope 105: 236240.CrossRefGoogle ScholarPubMed
Taylor, I. G., Irwin, J. (1978) Some audiological aspects of diabetes mellitus. Journal of Laryngology and Otology 92: 99113.CrossRefGoogle ScholarPubMed
Triana, R. J., Suits, G. W., Garrison, S., Prazma, J., Brechtelsbauer, P. B., Michaelis, O. E., Pillsbury, H. C. (1991) Inner ear damage secondary to diabetes mellitus. Archives of Otolaryngology – Head and Neck Surgery 117: 635640.CrossRefGoogle ScholarPubMed
Wackym, P. A., Linthicum, F. H. (1986) Diabetes mellitus and hearing loss: Clinical and histopathologic relationships. American Journal of Otolaryngology 7: 176182.Google ScholarPubMed
Williamson, J. R., Kilo, C. (1977) Current status of capillary basement membrane disease in diabetes mellitus. Diabetes 26: 6573.CrossRefGoogle ScholarPubMed
Williamson, J. R., Kilo, C. (1983) Capillary basement membranes in diabetes. Diabetes 32: 96100.CrossRefGoogle ScholarPubMed