Enzyme-induced posterior vitreous detachment in the rat produces increased lens nuclear pO2 levels

Experimental Eye Research

Volumn 88, Issue 2, 2009, Pages 286-292

  Giblin, F J ^a   Quiram, P A ^b   Leverenz, V R ^a   Baker, R M ^a   Dang, Loan ^a   Trese, M T ^b  

^a OAKLAND UNIVERSITY   (United States)

^b WILLIAM BEAUMONT HOSPITAL   (United States)

Author keywords

guinea pig; lens; microplasmin; nuclear cataract; oxygen; posterior vitreous detachment; rat; vitreous humor

Indexed keywords

HYALURONIDASE; OXYGEN; PLATINUM;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CATARACT; CONTROLLED STUDY; LIQUEFACTION; NONHUMAN; OXYGEN SENSING; PRIORITY JOURNAL; RAT; RETINA ISCHEMIA; VITREOUS BODY; VITREOUS BODY DETACHMENT;

ANIMALS; CATS; GUINEA PIGS; HYALURONOGLUCOSAMINIDASE; LENS NUCLEUS, CRYSTALLINE; MICROSCOPY, ELECTRON, SCANNING; MODELS, ANIMAL; OXYGEN; PEPTIDE FRAGMENTS; PLASMIN; RABBITS; RATS; RATS, INBRED BN; SPECIES SPECIFICITY; VITRECTOMY; VITREOUS BODY; VITREOUS DETACHMENT;

EID: 61849171238     PISSN: 00144835     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.exer.2008.09.003     Document Type: Article

References (51)

1. Alder V.A., Cringle S.J., and Constable I.J. The retinal oxygen profile in cats. Invest. Ophthalmol. Vis. Sci. 24 (1983) 30-36
2. Barbazetto I.A., Liang J., Chang S., Zheng L., Spector A., and Dillon J.P. Oxygen tension in the rabbit lens and vitreous before and after vitrectomy. Exp. Eye Res. 78 (2004) 917-924
3. Barton K.A., Shui Y.B., Petrash J.M., and Beebe D.C. Comment on: the Stokes-Einstein equation and the physiological effects of vitreous surgery. Acta Ophthalmol. Scand. 85 (2007) 339-340
4. Beebe D.C. Maintaining transparency: a review of the developmental physiology and pathophysiology of two avascular tissues. Semin. Cell Dev. Biol. 19 (2008) 125-133
5. Blankenship G.W., and Machemer R. Pars plana vitrectomy for the management of severe diabetic retinopathy: an analysis of results five years following surgery. Ophthalmology 85 (1978) 553-559
6. 2 gradients and countercurrent exchange in the cat vitreous humor near retinal arterioles and venules. Microvasc. Res. 45 (1993) 134-148
7. Cherfan G.M., Michels R.G., de B.S., Enger C., and Glaser B.M. Nuclear sclerotic cataract after vitrectomy for idiopathic epiretinal membranes causing macular pucker. Am. J. Ophthalmol. 111 (1991) 434-438
8. Cringle S., Yu D.Y., Alder V., Su E.N., and Yu P. Oxygen consumption in the avascular guinea pig retina. Am. J. Physiol. 271 (1996) H1162-H1165
9. Foos R.Y., and Wheeler N.C. Vitreoretinal juncture. Synchysis senilis and posterior vitreous detachment. Ophthalmology 89 (1982) 1502-1512
10. Gandorfer A., Rohleder M., Sethi C., Eckle D., Welge-Lussen U., Kampik A., Luthert P., and Charteris D. Posterior vitreous detachment induced by microplasmin. Invest. Ophthalmol. Vis. Sci. 45 (2004) 641-647
11. Gesell L.B., and Trott A. De novo cataract development following a standard course of hyperbaric oxygen therapy. Undersea Hyperb. Med. 34 (2007) 389-392
12. Giblin F.J., Padgaonkar V.A., Leverenz V.R., Lin L.R., Lou M.F., Unakar N.J., Dang L., Dickerson Jr. J.E., and Reddy V.N. Nuclear light scattering, disulfide formation and membrane damage in lenses of older guinea pigs treated with hyperbaric oxygen. Exp. Eye Res. 60 (1995) 219-235
13. Gottlieb J.L., Antoszyk A.N., Hatchell D.L., and Saloupis P. The safety of intravitreal hyaluronidase. A clinical and histologic study. Invest. Ophthalmol. Vis. Sci. 31 (1990) 2345-2352
14. Grigorian R., Bhagat N., Lanzetta P., Tutela A., and Zarbin M. Pars plana vitrectomy for refractory diabetic macular edema. Semin. Ophthalmol. 18 (2003) 116-120
15. Harocopos G.J., Shui Y.B., McKinnon M., Holekamp N.M., Gordon M.O., and Beebe D.C. Importance of vitreous liquefaction in age-related cataract. Invest. Ophthalmol. Vis. Sci. 45 (2004) 77-85
16. Hikichi T., Kado M., and Yoshida A. Intravitreal injection of hyaluronidase cannot induce posterior vitreous detachment in the rabbit. Retina 20 (2000) 195-198
17. Holekamp N.M., Shui Y.B., and Beebe D.C. Vitrectomy surgery increases oxygen exposure to the lens: a possible mechanism for nuclear cataract formation. Am. J. Ophthalmol. 139 (2005) 302-310
18. Hum T.P., and Augusteyn R.C. The nature of disulphide bonds in rat lens proteins. Curr. Eye Res. 6 (1987) 1103-1108
19. Landers III M.B., Stefansson E., and Wolbarsht M.L. Panretinal photocoagulation and retinal oxygenation. Retina 2 (1982) 167-175
20. Lee B., Litt M., and Buchsbaum G. Rheology of the vitreous body. Part I: viscoelasticity of human vitreous. Biorheology 29 (1992) 521-533
21. Leong C.L., O'Connor P.M., Eppel G.A., Anderson W.P., and Evans R.G. Measurement of renal tissue oxygen tension: systematic differences between fluorescence optode and microelectrode recordings in anaesthetized rabbits. Nephron Physiol. 108 (2008) 11-17
22. Linsenmeier R.A., Goldstick T.K., Blum R.S., and Enroth-Cugell C. Estimation of retinal oxygen transients from measurements made in the vitreous humor. Exp. Eye Res. 32 (1981) 369-379
23. Linsenmeier R.A., and Yancey C.M. Effects of hyperoxia on the oxygen distribution in the intact cat retina. Invest. Ophthalmol. Vis. Sci. 30 (1989) 612-618
24. Margherio R.R., Cox Jr. M.S., Trese M.T., Murphy P.L., Johnson J., and Minor L.A. Removal of epimacular membranes. Ophthalmology 92 (1985) 1075-1083
25. Maurice D.M. Protein dynamics in the eye studied with labelled proteins. Am. J. Ophthalmol. 47 (1959) 361-368
26. McNulty R., Wang H., Mathias R.T., Ortwerth B.J., Truscott R.J., and Bassnett S. Regulation of tissue oxygen levels in the mammalian lens. J. Physiol. 559 (2004) 883-898
27. Michels R.G. Vitrectomy for macular pucker. Ophthalmology 91 (1984) 1384-1388
28. Nagai, K., Sasaki, H., Honda, R., Kanazawa, Y., Sakamoto, Y., Qu, J., Sasaki, K., 2007. Change of light scattering intensity in eyes with posterior vitreous detachment: monzon eye study. Abstracts. In: US-Japan Cooperative Cataract Research Group Meeting, p. HT-5.
29. Nagai N., Demarsin E., Van H.B., Wouters S., Cingolani D., Laroche Y., and Collen D. Recombinant human microplasmin: production and potential therapeutic properties. J. Thromb. Haemost. 1 (2003) 307-313
30. Ogura Y., Takanashi T., Ishigooka H., and Ogino N. Quantitative analysis of lens changes after vitrectomy by fluorophotometry. Am. J. Ophthalmol. 111 (1991) 179-183
31. Ormerod L.D., Edelstein M.A., Schmidt G.J., Juarez R.S., Finegold S.M., and Smith R.E. The intraocular environment and experimental anaerobic bacterial endophthalmitis. Arch. Ophthalmol. 105 (1987) 1571-1575
32. Palmquist B.M., Philipson B., and Barr P.O. Nuclear cataract and myopia during hyperbaric oxygen therapy. Br. J. Ophthalmol. 68 (1984) 113-117
33. 2 in the retina of anesthetized miniature pigs in normoxia and hyperoxia. Exp. Eye Res. 49 (1989) 347-360
34. Quiram P.A., Leverenz V.R., Baker R.M., Dang L., Giblin F.J., and Trese M.T. Microplasmin-induced posterior vitreous detachment affects vitreous oxygen levels. Retina 27 (2007) 1090-1096
35. Sakaue H., Negi A., and Honda Y. Comparative study of vitreous oxygen tension in human and rabbit eyes. Invest. Ophthalmol. Vis. Sci. 30 (1989) 1933-1937
36. Sakuma T., Tanaka M., Mizota A., Inoue J., and Pakola S. Safety of in vivo pharmacologic vitreolysis with recombinant microplasmin in rabbit eyes. Invest. Ophthalmol. Vis. Sci. 46 (2005) 3295-3299
37. Schocket S.S., Esterson J., Bradford B., Michaelis M., and Richards R.D. Induction of cataracts in mice by exposure to oxygen. Isr. J. Med. Sci. 8 (1972) 1596-1601
38. Sebag J., Ansari R.R., and Suh K.I. Pharmacologic vitreolysis with microplasmin increases vitreous diffusion coefficients. Graefes Arch. Clin. Exp. Ophthalmol. 245 (2007) 576-580
39. Seddon B.M., Honess D.J., Vojnovic B., Tozer G.M., and Workman P. Measurement of tumor oxygenation: in vivo comparison of a luminescence fiber-optic sensor and a polarographic electrode in the p22 tumor. Radiat. Res. 155 (2001) 837-846
40. Shui Y.B., Fu J.J., Garcia C., Dattilo L.K., Rajagopal R., McMillan S., Mak G., Holekamp N.M., Lewis A., and Beebe D.C. Oxygen distribution in the rabbit eye and oxygen consumption by the lens. Invest. Ophthalmol. Vis. Sci. 47 (2006) 1571-1580
41. Simpanya M.F., Ansari R.R., Suh K.I., Leverenz V.R., and Giblin F.J. Aggregation of lens crystallins in an in vivo hyperbaric oxygen guinea pig model of nuclear cataract: dynamic light-scattering and HPLC analysis. Invest. Ophthalmol. Vis. Sci. 46 (2005) 4641-4651
42. Stefansson E. Ocular oxygenation and the treatment of diabetic retinopathy. Surv. Ophthalmol. 51 (2006) 364-380
43. Stefansson E., and Loftsson T. The Stokes-Einstein equation and the physiological effects of vitreous surgery. Acta Ophthalmol. Scand. 84 (2006) 718-719
44. Stefansson E., Novack R.L., and Hatchell D.L. Vitrectomy prevents retinal hypoxia in branch retinal vein occlusion. Invest. Ophthalmol. Vis. Sci. 31 (1990) 284-289
45. Tachi N., and Ogino N. Vitrectomy for diffuse macular edema in cases of diabetic retinopathy. Am. J. Ophthalmol. 122 (1996) 258-260
46. Truscott R.J. Age-related nuclear cataract-oxidation is the key. Exp. Eye Res. 80 (2005) 709-725
47. Uyama C. Diffusion model of a cat eye. In: Kessler M. (Ed). Oxygen Supply: Theoretical and Practical Aspects of Oxygen Supply and Microcirculation of Tissue (1973), University Park Press, Baltimore 64-66
48. Wen B., Urano M., Humm J.L., Seshan V.E., Li G.C., and Ling C.C. Comparison of Helzel and OxyLite systems in the measurements of tumor partial oxygen pressure (pO2). Radiat. Res. 169 (2008) 67-75
49. Yu D.Y., and Cringle S.J. Oxygen distribution and consumption within the retina in vascularised and avascular retinas and in animal models of retinal disease. Prog. Retin. Eye Res. 20 (2001) 175-208
50. Yu D.Y., Cringle S.J., and Alder V.A. The response of rat vitreal oxygen tension to stepwise increases in inspired percentage oxygen. Invest. Ophthalmol. Vis. Sci. 31 (1990) 2493-2499
51. Yu D.Y., Cringle S.J., Alder V.A., Su E.N., and Yu P.K. Intraretinal oxygen distribution and choroidal regulation in the avascular retina of guinea pigs. Am. J. Physiol. 270 (1996) H965-H973