Morphological Evidence of Vestibular Pathology in Long-Term Experimental Diabetes Mellitus: I. Microvascular Changes

References

• Jørgensen M B, Buch N H. Studies on inner-ear function and cranial nerves in diabetics. Acta Otolaryngol (Stockh) 1961; 53: 350–64
   PubMedGoogle Scholar
• Axelsson A, Fagerberg S-E. Auditory function in diabetics. Acta Otolaryngol (Stockh) 1968; 66: 49–64
   PubMedGoogle Scholar
• Axelsson A, Sigroth K, Vertes D. Hearing in diabetes. Acta Otolaryngol (Stockh) 1978; 2–23, Suppl 356
   Google Scholar
• Friedman S A, Schulma R H, Weiss S. Hearing and diabetic neuropathy. Arch Intern Med 1975; 135: 573–6
   PubMed Web of Science ®Google Scholar
• Makishima K, Tanaka K. Pathological changes of the inner ear and central auditory pathway in diabetics. Ann Otol Rhinol Laryngol 1971; 80: 218–28
   PubMed Web of Science ®Google Scholar
• Naufal P M, Schuknecht H F. Vestibular, facial and oculomotor neuropathy in diabetes melhtus. Arch Otolaryngol 1972; 96: 468–74
   PubMed Web of Science ®Google Scholar
• Taylor I G, Irwin J. Some audiological aspects of diabetes mellitus. J Laryngol Otol 1978; 92: 99–113
   PubMed Web of Science ®Google Scholar
• Zelenka J, Zozak P. Disorder in blood supply of the inner ear as early symptom of diabetic angiopathy. J Laryngol Otol 1965; 79: 314–9
   PubMedGoogle Scholar
• Harner S G. Hearing in adult-onset diabetes mellitus. Otolaryngol Head Neck Surg 1981; 89: 322–7
   PubMed Web of Science ®Google Scholar
• Jokelainen I T, Webb D R, Yush E D. A combined electron microscopic-microangiographic methodology for cerebrovascular studies. J Ultrastruct Res 1980; 71: 116–25
   PubMedGoogle Scholar
• Baird I L, Winborn W B, Bockman D E. A technique of decalification suited to electron microscopy of tissues closely associated with bone. Anat Rec 1967; 159: 281–90
   PubMedGoogle Scholar
• Østerby R. Early phases in the development of diabetic glomerulopathy. A quantitative electron microscopic study. Acta Med Scand 1975; 3–82, Suppl 574
   Google Scholar
• Kilo C, Vogler N, Williamson J R. Muscle capillary basement membrane related to aging and to diabetes mellitus. Diabetes 1972; 21: 884–905
   Google Scholar
• Yodaiken R E, Seftel H C, Rubenstein A N. Ultrastructure of dermal capillaries of Africans in South Africa. Diabetes 1967; 16: 191–7
   PubMedGoogle Scholar
• Chazar B I, Kuwabara T, Balodimos M C, Beethan W P. The reactivity and ultrastructure of conjunctival microaneurysms in diabetes. Diabetologia 1969; 5: 331–8
   PubMedGoogle Scholar
• Fenton B M, Zweifach B W, Worthen D M. Quantitative morphometry of conjunctival microcircu-lation in diabetes mellitus. Microvascular Res 1978; 18: 153–66
   Google Scholar
• Cogan D G, Kuwabara T K. Ocular microangiopathy in diabetes. Vascular complications of diabetes mellitus. CV, Mosby, St Louis 1967; 53–63
   Google Scholar
• Bischoff A. Die diabetische Neuropathie. Praxis 1965; 54: 723–31
   PubMedGoogle Scholar
• Bischoff A. Morphology of diabetic neuropathy. Horm Metab Res 1980; 9(Suppl)18–28
   Google Scholar
• Cambell M JA. A light and electron microscopic study of blood vessels from the gingival tissues of non-diabetic and diabetic patients. Aust Dent J 1971; 16: 235–9
   PubMedGoogle Scholar
• Fischer V W, Barner H B, Leskiw M L. Capillary basal laminar thickness in diabetic human myocardium. Diabetes 1979; 28: 713–9
   PubMedGoogle Scholar
• Østerby Hansen R, Lundbaek K, Olsen T S, Orskov K. Kidney lesions in rats with severe long term alloxan diabetes (III glomerular ultrastructure). Lab Invest 1967; 17: 675–92
   PubMedGoogle Scholar
• Mauer S M, Steffes M W, Michael A F, Brown D M. Studies of diabetic nephropathy in animals and man. Diabetes 1976; 25(Suppl 2)50–7
   Google Scholar
• Leuenberger P, Camlron S, Stauffacher W, Renold A E, Babel J. Ocular lesions in rats rendered chronically diabetic with streptozotocin. Opthalmol Res 1971; 2: 189–204
   Google Scholar
• Marliss E B, Nakhooda A F, Paussier P, Sima A AF. The diabetc syndrome of the ‘BB’ Wistar rat: Possible relevance to type 1 (insulin-dependent) diabetes in man. Diabetologia 1982; 22: 225–32
   PubMed Web of Science ®Google Scholar
• Giacomelli F, Wiener J. Primary myocardial disease in the diabetic mouse. Lab Invest 1979; 40: 460–7
   PubMed Web of Science ®Google Scholar
• Vracko R. Skeletal muscle capillaries in diabetics. A quantitative analysis. Circulation 1970; 41: 271–83
   PubMed Web of Science ®Google Scholar
• Østerby R. Basement membrane morphology in diabetes mellitus. Diabetes mellitus, M Ellenberg, H Rifkin. Medical Examination Publishing Co Inc, New York 1983; 323–41
   Google Scholar
• Deckert T, Egeberg J, Frimodt-Moller C, Sander E, Svajgaard A. Basement membrane thickness, insulin antibodies and HLA antigens in long standing insulin dependent diabetics with and without severe retinopathy. Diabetologia 1979; 17: 91–6
   PubMedGoogle Scholar
• Dunn P J, Donald R A, Day T, Stewart J M, Stewart A W. The association between diabetic retinopathy and skeletal muscle thickening corrected for the influence of age and duration of diabetes. Diabetes 1979; 28: 858–64
   PubMedGoogle Scholar
• Ashton N. Vascular basement membrane changes in diabetic retinopathy. Br J Ophthal 1974; 58: 344–66
   PubMed Web of Science ®Google Scholar
• Robinson W G, Kador P F, Kinoshita J H. Retinal capillaries: basement membrane thickening by galactosemia prevented with aldose reductase inhibitor. Science 1983; 221: 1177–9
   PubMed Web of Science ®Google Scholar
• Beyer-Mears A, Ku L, Chen M P. Glomerular polyol accumulation in diabetes and its prevention by oral sorbinil. Diabetes 1984; 33: 604–7
   PubMedGoogle Scholar
• Alpert J S, Coffman J D, Balodimos M C, Koncz L, Soeldner J S. Capillary permeability and blood flow in skeletal muscle of patients with diabetes mellitus and genetic prediabetes. New Engl 3 Med 1972; 286: 454–60
   PubMed Web of Science ®Google Scholar
• Leinonen H, Matikainen E, Juntunen J. Permeability and morphology of skeletal muscle capillaries in type 1 (insulin-dependent) diabetes mellitus. Diabetologia 1982; 22: 158–62
   PubMedGoogle Scholar
• Bassiouny A R, Rosenberg H, McDonald J L. Glycosylated collagen is antigenic. Diabetes 1983; 32: 1182–4
   PubMedGoogle Scholar
• Tomoda K, Yoo T J. Type II collagen distribution in the inner ear. Abstracts of the sixth midwinter research meeting of the Association for Research in Otolaryngology. 1983, D J Lim. 36
   Google Scholar
• Quick C A, Fish A, Brown C. The relationship between cochlea and kidney. Laryngoscope 1973; 83: 1469–82
   PubMed Web of Science ®Google Scholar
• Yoo T J, Yazawa Y, Tomoda K, Floyd T. Type II collagen-induced autoimmune endolymphatic hydrops in guinea pig. Science 1983; 222: 65–7
   PubMed Web of Science ®Google Scholar
• Jørgensen M B. The inner ear in diabetes mellitus. Arch Otol 1961; 74: 373–81
   PubMed Web of Science ®Google Scholar
• Costa O A. Inner ear pathology in experimental diabetes. Laryngoscope 1967; 77: 68–75
   PubMed Web of Science ®Google Scholar
• Makishima K, Tanaka K. Pathological changes of the inner ear and central auditory pathway in diabetics. Ann Otol Rhinol Laryngol 1971; 80: 218–28
   PubMed Web of Science ®Google Scholar
• Kovar M. The inner ear in diabetes mellitus. Otorhinol 1973; 35: 42–51
   Google Scholar
• Bell M A, Ball M J. Morphometric comparison of hippocampal microvasculature in aging and demented people: diameters and densities. Acta Neuropathol 1981; 53: 299–318
   PubMed Web of Science ®Google Scholar
• Paljärvi L, Rehncrona S, Söderfeldt B, Olsson Y, Kalimo H. Brain lactic acidosis and ischemic cell damage: quantitative ultrastructural changes in capillaries of rat cerebral cortex. Acta Neuropathol 1983; 60: 232–40
   PubMedGoogle Scholar
• Stebbens W E. Anatomy and structure of blood vessels. Hemodynamics and the blood vessel vall, W E Stebbens. Thomas, Springfield 1979; 3–74
   Google Scholar
• Zweifach B W, Lipowsky H H. Quantitative studies of microvascular hemodynamics of cat mesentery and rabbit omentum. Circ Res 1977; 41: 380–90
   PubMedGoogle Scholar
• Schmid-Schonbein H, Volger E. Red-cell aggregation and red-cell deformability in diabetes. Diabetes 1976; 25(Suppl 2)897–904
   PubMedGoogle Scholar
• McMillan D E, Utterback N G, La Puma J. Reduced erythrocyte deformability in diabetes. Diabetes 1978; 27: 895–901
   PubMed Web of Science ®Google Scholar
• McMillan D E, Gion K M. Glycosylated hemoglobin and reduced erythrocyte deformability in diabetes. Horm Metab Res 1981; 11(Suppl)108–11
   Google Scholar
• Otsuji S, Baba Y, Kamada T. Erythrocyte membrane microviscosity in diabetes. Horm Metab Res 1981; 11(Suppl)97–102
   Google Scholar
• McMillan D E. Pathophysiofogy of diabetic macro- and microvascular disease. Diabetes mellitus, M Ellenberg, H Rifkin. Medical Examination Publishing Co Inc, New York 1983; 343–59
   Google Scholar
• Bunn H F, Gabbay K H, Gallop P M. The glycosylation of hemoglobin; relevance to diabetes mellitus. Science 1978; 200: 271–279
   Google Scholar
• Ditzel J. Oxygen transport impairment in diabetes. Diabetes 1976; 25(Suppl 2)832–8
   PubMedGoogle Scholar
• Samaja M, Melotti D, Carenini A, Pozza G. Glycosylated haemoglobins and the oxygen affinity of whole blood. Diabetologia 1982; 23: 399–402
   PubMedGoogle Scholar