Decreased keratocyte death after laser-assisted subepithelial keratectomy and photorefractive keratectomy in rabbits

Journal of Cataract and Refractive Surgery

Volumn 30, Issue 9, 2004, Pages 1998-2004

  Laube, Thomas ^a   Wissing, Susanne ^a   Theiss, Carsten ^a   Brockmann, Claudia ^a   Steuhl, Klaus Peter ^a   Meller, Daniel ^a,b  

^a University of Essen ^*

^b UNIVERSITY OF DUISBURG ESSEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA FRAGMENT;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CELL COUNT; CELL DEATH; CELL SIZE; CELL ULTRASTRUCTURE; CHROMATIN CONDENSATION; CONTROLLED STUDY; CORNEA CELL; CORNEA STROMA; DNA DETERMINATION; EXCIMER LASER; GERMANY; INTERMETHOD COMPARISON; LASER EPITHELIAL KERATOMILEUSIS; NICK END LABELING; NONHUMAN; PHOTOREFRACTIVE KERATECTOMY; POSTOPERATIVE PERIOD; PRIORITY JOURNAL; RABBIT; STROMA; TIME; TRANSMISSION ELECTRON MICROSCOPY; UNIVERSITY; WOUND HEALING;

ANIMALS; APOPTOSIS; CELL COUNT; CELL SURVIVAL; CORNEAL STROMA; FIBROBLASTS; IN SITU NICK-END LABELING; KERATECTOMY, PHOTOREFRACTIVE, EXCIMER LASER; KERATOMILEUSIS, LASER IN SITU; MODELS, ANIMAL; RABBITS; WOUND HEALING;

EID: 4444339501     PISSN: 08863350     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcrs.2004.01.040     Document Type: Article

References (41)

1. Trokel S.L., Srinivasan R., Braren B. Excimer laser surguery of the cornea. Am J Ophthalmol. 96:1983;710-715
2. Corbett M.C., Prydal J.I., Verma S., et al. An in vivo investigation of the structures responsible for corneal haze after photorefractive keratectomy and their effect on visual function. Ophthalmology. 103:1996;1366-1380
3. Wang Z., Chen J., Yang B. Comparison of laser in situ keratomileusis and photorefractive keratectomy to correct myopia from -1.25 to -6.00 diopters. J Refract Surg. 13:1997;528-534
4. Pallikaris I.G., Papatzanaki M.E., Siganos D.S., Tsilimbaris M.K. A corneal flap technique for laser in situ keratomileusis; human studies. Arch Ophthalmol. 109:1991;1699-1702
5. Pallikaris I.G., Papatzanaki M.E., Stathi E.Z., et al. Laser in situ keratomileusis. Lasers Surg Med. 10:1990;463-468
6. Wilson S.E. Lasik. management of common complications Cornea. 17:1998;459-467
7. Walker M.B., Wilson S.E. Incidence and prevention of epithelial growth within the interface after laser in situ keratomileusis. Cornea. 19:2000;170173
8. Melki S.A., Azar D.T. LASIK complications. etiology, management, and prevention Surv Ophthalmol. 46:2001;95-116
9. Wang Z., Chen J., Yang B. Posterior corneal surface topographic changes after laser in situ keratomileusis are related to residual corneal bed thickness. Ophthalmology. 106:1999;406-409. discussion by RK Maloney, 409-410
10. Shah S., Sebai Sarhan A.R., Doyle S.J., et al. The epithelial flap for photorefractive keratectomy. Br J Ophthalmol. 85:2001;393-396
11. Anderson N.J., Beran R.F., Schneider T.L. Epi-LASEK for the correction of myopia and myopic astigmatism. J Cataract Refract Surg. 28:2002;1343-1347
12. Claringbold T.V. II Laser-assisted subepithelial keratectomy for the correction of myopia. J Cataract Refract Surg. 28:2002;18-22
13. Shahinian L. Jr. Laser-assisted subepithelial keratectomy for low to high myopia and astigmatism. J Cataract Refract Surg. 28:2002;1334-1342
14. Lee J.B., Seong G.J., Lee J.H., et al. Comparison of laser epithelial keratomileusis and photorefractive keratectomy for low to moderate myopia. J Cataract Refract Surg. 27:2001;565-570
15. Campos M., Raman S., Lee M., McDonnell P.J. Keratocyte loss after different methods of de-epithelialization. Ophthalmology. 101:1994;890-894
16. Campos M., Szerenyi K., Lee M., et al. Keratocyte loss after corneal deepithelialization in primates and rabbits. Arch Ophthalmol. 112:1994;254-260
17. Kim W.-J., Shah S., Wilson S.E. Differences in keratocyte apoptosis following transepithelial and laser-scrape photorefractive keratectomy in rabbits. J Refract Surg. 14:1998;526-533
18. Dohlman C.H., Gasset A.R., Rose J. The effect of the absence of corneal epithelium or endothelium on the stromal keratocytes. Invest Ophthalmol. 7:1968;520-534
19. Wilson S.E., He Y.-G., Weng J., et al. Epithelial injury induces keratocyte apoptosis. hypothesized role for the interleukin-1 system in the modulation of corneal tissue organization and wound healing Exp Eye Res. 62:1996;325-337
20. Wilson S.E. Role of apoptosis in wound healing in the cornea. Cornea. 19(suppl):2000;S7-S12
21. Wilson S.E., Mohan R.R., Hong J.-W., et al. The wound healing response after laser in situ keratomileusis and photorefractive keratectomy; elusive control of biological variability and effect on custom laser vision correction. Arch Ophthalmol. 119:2001;889-896
22. Gao J., Gelber-Schwalb T.A., Addeo J.V., Stern M.E. Apoptosis in the rabbit cornea after photorefractive keratectomy. Cornea. 16:1997;200-208
23. Merayo-Lloves J., Yáñez B., Mayo A., et al. Experimental model of corneal haze in chickens. J Refract Surg. 17:2001;696-699
24. Park W.C., Tseng S.C.G. Modulation of acute inflammation and keratocyte death by suturing, blood, and amniotic membrane in PRK. Invest Ophthalmol Vis Sci. 41:2000;2906-2914
25. Kim S.-Y., Sah W.-J., Lim Y.-W., Hahn T.-W. Twenty percent alcohol toxicity on rabbit corneal epithelial cells; electron microscopic study. Cornea. 21:2002;388-392
26. Helena M.C., Baerveldt F., Kim W.-J., Wilson S.E. Keratocyte apoptosis after corneal surgery. Invest Ophthalmol Vis Sci. 39:1998;276-283
27. Chen C.C., Chang J.-H., Lee J.B., et al. Human corneal epithelial cell viability and morphology after dilute alcohol exposure. Invest Ophthalmol Vis Sci. 43:2002;2593-2602
28. Browning A.C., Shah S., Dua H.S., et al. Alcohol debridement of the corneal epithelium in PRK and LASEK. an electron microscopic study Invest Ophthalmol Vis Sci. 44:2003;510-513
29. Nakamura K., Kurosaka D., Bissen-Miyajima H., Tsubota K. Intact corneal epithelium is essential for the prevention of stromal haze after laser assisted in situ keratomileusis. Br J Ophthalmol. 85:2001;209-213
30. Wilson S.E., Liu J.J., Mohan R.R. Stromal-epithelial interactions in the cornea. Prog Retin Eye Res. 18:1999;293-309
31. Li D.-Q., Tseng S.C.G. Differential regulation of keratinocyte growth factor and hepatocyte growth factor/scatter factor by different cytokines in human corneal and limbal fibroblasts. J Cell Physiol. 172:1997;361-372
32. Vesaluoma M., Teppo A.-M., Grönhagen-Riska C., Tervo T. Release of TGF-β1 and VEGF in tears following photorefractive keratectomy. Curr Eye Res. 16:1997;19-25
33. Schultz G., Khaw P.T., Oxford K., et al. Growth factors and ocular wound healing. Eye. 8:1994;184-187
34. Baldwin H.C., Marshall J. Growth factors in corneal wound healing following refractive surgery. a review Acta Ophthalmol Scand. 80:2002;238-247
35. Wilson S.E., Kim W.-J. Keratocyte apoptosis. implications on corneal wound healing, tissue organization, and disease Invest Ophthalmol Vis Sci. 39:1998;220-226
36. Lee J.B., Choe C.-M., Kim H.S., et al. Comparison of TGF-β1 in tears following laser subepithelial keratomileusis and photorefractive keratectomy. J Refract Surg. 18:2002;130-134
37. Lee Y.-C., Wang I.-J., Hu F.-R., Kao W.W.-Y. Immunohistochemical study of subepithelial haze after phototherapeutic keratectomy. J Refract Surg. 17:2001;334-341
38. β modulates stromal fibrosis but not regression of photoablative effect following PRK. Curr Eye Res. 17:1998;736-747
39. Choi Y.S., Kim J.Y., Wee W.R., Lee J.H. Effect of the application of human amniotic membrane on rabbit corneal wound healing after excimer laser photorefractive keratectomy. Cornea. 17:1998;389-395
40. Wang M.X., Gray T.B., Park W.C., et al. Reduction in corneal haze and apoptosis by amniotic membrane matrix in excimer laser photoablation in rabbits. J Cataract Refract Surg. 27:2001;310-319
41. Lim L., Tan D.T.H., Chan W.K. Therapeutic use of Bausch & Lomb PureVision contact lenses. CLAO J. 27:2001;179-185