Characterization of acute and delayed ocular lesions induced by sulfur mustard in rabbits

Reference

• Papirmeister B, Feister AJ, Robinson SI, Ford RD. Medical defense against mustard gas, toxic mechanisms and phar-macological implications, 1991, pp. 21–23, 61–66. CRC Broca Raton.
   Google Scholar
• Wormser U Toxicology of mustard gas. TIPS. 1991;12:164-167.
   Google Scholar
• Borak J, Sidell FR. Agents of chemical warfare: Sulfur mustard. Ann Emerg Med. 1992;21:303–308.
   PubMed Web of Science ®Google Scholar
• Solberg Y, Alcalay M, Belkin M. Ocular injury by mustard gas. Surv Ophtalmol. 1997;41:461–466.
   PubMed Web of Science ®Google Scholar
• Berens C, Hartmann E. The effect of war gases and other chemicals on the eyes of the civilian population. Bull NY Acad Med. 1943;19:356–367.
   PubMedGoogle Scholar
• Brozetti JJ, Finger AV, Patterson OC. Ocular manifestations of sulfur mustard exposure. Proc Med Defence Biosci Rev. 1996;11:1202-1209. US. Army Medical Research and Material Command, MD.
   Google Scholar
• Geeraets WJ, Abedi S, Blanke RV. Acute corneal injury by mustard gas. Southern Med J. 1977;70:348–350.
   PubMed Web of Science ®Google Scholar
• Derby GS. Effects of mustard gas on the eyes. Am J Med Sci. 1918;156:733–736.
   Google Scholar
• Mellor SG, Rice P, Cooper GJ. Vesicant burns. Br J Plast Surg. 1991;44:434–437.
   PubMedGoogle Scholar
• De Courcy TL. A case of mustard gas keratitis under constant observation for a period of twenty years. Br J Ophthalmol. 1943;27:54–60.
   PubMedGoogle Scholar
• Blodi FC. Delayed mustard gas keratopathy. Am J Oph-thalmol. 1953;36:1575.
   PubMed Web of Science ®Google Scholar
• Blodi FC. Mustard gas keratopathy. Int Ophthalmol Clin. 1971;11:1–13.
   PubMedGoogle Scholar
• Neame H. Late results after mustard gas burn of the eyes. Proc Royal Soc Med. 1928;22:25–26.
   Google Scholar
• Willems JL. Clinical management of mustard gas casual-ties. Ann Medicinae Militaris Belgicae. 1989;3.
   Google Scholar
• Javadi MA, Einollahi B, Jadidi K, Karimian F, Zarc M, Minlehghan A. (1998) Mustard gas keratitis. (Abstract) Ann Meeting of the American Academy of Ophthalmology. New Orleans, Louisiana.
   Google Scholar
• Pleyer U, Sherif Z, Baatz H, Hartmann C. Delayed mustard gas keratopathy: Clinical findings and confocal microscopy. Am J Ophthalmol. 1999;128:506–507.
   PubMed Web of Science ®Google Scholar
• Hughes WF. Mustard gas injuries to the eyes. Arch Oph-thalmol. 1942;582–601.
   Google Scholar
• Friedenwald JS, members of the staff of the Wilmer Insti-tute, John Hopkins hospital. Studies on the physiology, biochemistry and cytopathology of the cornea in relation to injury by mustard gas and allied toxic agents. Bull Johns Hopkins Hospital. 1948;82:81–352.
   Google Scholar
• Patterson OC, Finger A. Quantitative assays of sulfur mustard induced ocular injury in a rabbit model with newer ophthalmic technology. Proc Med Defence Biosci Rev. 1996;11:1324-1333. US. Army Medical Research and Material Command, MD.
   Google Scholar
• Petrali JP, Miskena FJ, Hamilton TA, Finger AV, Jarmy SJ. Sulfur mustard toxicity of the rabbit eye: An ultrastruc- tural study. J Toxicol & Cut & Ocular Toxicol. 1997;16: 227–237.
   Web of Science ®Google Scholar
• Arroyo CM, Schafer RJ, Kurt EM, Broomfield CA, Carmichael AJ. Response of normal human keratinocytes to sulfur mustard (HD): Cytokine release using non-enzymatic detachment procedure. Hum Exp Toxicol. 1999; 18:1–11.
   Google Scholar
• Lardot C, Dubois V, Lison D. Sulfur mustard upregulates the expression of interleukin-8 in cultured human ker-atinocytes. Toxicol Lett. 1999;110: 29–33.
   Google Scholar
• Anderson ME. Determination of glutathione and glu-tathione disulfide in biological samples. In: Meister A, ed. Glutamate, Glutamine, Glutathione and Related Com-pounds: Methods in Enzymology. 1985;113:548–555.
   Google Scholar
• Bhuyan KC, Bhuyan DK. Regulation of hydrogen peroxide in eye humors. Effect of 3-amino-1H-1,2,4-triazole on catalase and glutathione peroxidase of rabbit eye. BBA. 1977;497: 641–651.
   Google Scholar
• Kadar T, Amir A, Fishbine E, Chapman S, Liani H, Sahar R, Rabinovitz I, Simon G, Frishman G, Sheivitz R, Turetz J. The potential therapy of steroids against ocular lesions induced by sulfur mustard vapor in rabbits. Proc Med Defence Biosci Rev. 1996;11:845-852. U.S. Army Medical Research and Material Command, MD.
   Google Scholar
• Amir A, Turetz J, Chapman S, Fishbine E, Meshulam J, Sahar R, Liani H, Gilat E, Frishman G, Kadar T. The beneficial effects of topical anti-inflammatory drugs against HD-induced ocular lesions in rabbits. Proc Med Defence Biosci Rev. 1998,1–11. US. Army Medical Research and Material Command, MD.
   Google Scholar
• Mann I, Pullinger BD. A study of mustard gas lesions of the eyes of rabbits and men. Proc Royal Soc Med. 1942;35:229–244.
   PubMedGoogle Scholar
• Mann I. A Study of eighty-four cases of delayed mustard gas keratitis fitted with contact lenses. Br J Ophthalmol. 1944;28:441–447.
   PubMedGoogle Scholar
• Varma SD, Devamanoharan PS, Ali AH, Henein M, Petrali J, Brozetti J, Lehriert E. Corneal damage by half mustard (2-chloroethyl ethyl sulfide, CEES) in vitro preventive studies: a histological and electron microscopic evaluation. J Ocular Pharmacol Therap. 1998;14: 413–428.
   Google Scholar
• Klein EM, Bito LZ. Species variation in the pathophysio-logic responses of vertebrate eyes to a chemical irritant, nitrogen mustard. Invest. Ophthalmol Vis Sci. 1983; 24:184–191.
   PubMed Web of Science ®Google Scholar
• Camras CB, Bito LZ. The pathophysiological effects of nitrogen mustard on rabbit eyes. I. The biphasic intraocu-lar pressure response and the role of prostaglandins. Exp Eye Res. 1980;30:41–52.
   PubMed Web of Science ®Google Scholar
• Camras CB, Bito LZ. The pathophysiological effects of nitrogen mustard on rabbit eyes. II. The inhibition of the initial hypertensive phase by capsaicin and the apparent role of substance P. Invest Ophthalmol Vis Sci. 1980; 19:423–428.
   Google Scholar
• Bito LZ. Species differences in the response of the eye to irritation and trauma: A hypothesis of divergence in ocular defense mechanisms and the choice of experi- mental animals for eye research. Exp Eye Res. 1984;39: 807–829.
   PubMed Web of Science ®Google Scholar
• Bazan NG, Allan G. Signal transduction and gene ex-pression in the eye: A contemporary view of the pro-inflammatory, anti-inflammatory and modulatory roles of prostaglandins and other bioactive lipids. Surv Ophthalmol. 1997;41:S23—S34.
   Web of Science ®Google Scholar
• Dua HS, Azuzrz-Blanco A. Limbal stem cells of the corneal epithelium. Surv Ophthalmol. 2000;44:415–425.
   PubMed Web of Science ®Google Scholar
• Tseng SCG. Regulation and clinical implications of corneal epithelial stem cells. Molecular Biol Reports. 1996; 23:47–58.
   PubMed Web of Science ®Google Scholar
• Riley MV, Meyer RIP, Yates EM. Glutathione in the aqueous humor of human and other species. Invest Ophthalmol Vis Sci. 1980;19:94–96.
   PubMed Web of Science ®Google Scholar
• Eliason JA. Leukocytes and experimental corneal vascularization. Invest Ophthalmol Vis Sci. 1978;17:1087–1095.
   PubMed Web of Science ®Google Scholar
• Applgate LA, Leg RD. DNA damage is involved in the induction of °pacification and neovascularization of the cornea by ultraviolet radiation. Exp Eye Res. 1991;52: 493–497.
   PubMed Web of Science ®Google Scholar
• Cogan DG. Corneal vascularization. Invest Ophthalmol. 1962;1:253–261.
   Google Scholar
• Campbell FW, Michaelson IC. Blood vessel formation in the cornea. Br J Ophthalmol. 1949;33:248.
   PubMed Web of Science ®Google Scholar
• Amano S, Rohan R, Kuroki M, Tolentino M, Adamis AR Requirement for vascular endothelial growth factor in wound- and inflammation-related corneal neovasculariza-tion. Invest Ophthalmol Vis Sci. 1998;39:18–22.
   PubMed Web of Science ®Google Scholar
• Sonoda K, Sakamoto T, Yoshikawa H, Ashzuka S, Ohshima Y, Kishihara K, Nomoto K, Ishibashi T, Inomata H. Inhibi-tion of corneal inflammation by the topical use of Ras farnesyltransferase inhibitors: Selective inhibition of macrophage localization. Invest Ophthalmol Vis Sci. 1998;39:2245–2251.
   Google Scholar
• Lee P, Wang CC, Adamis AR Ocular neovascularization: an epidemiologic review. Surv Ophthalmol. 1998;43:245–269.
   PubMed Web of Science ®Google Scholar
• Fromer CH, Klintworth GK. An evaluation of the role of leukocytes in the pathogenesis of experimentally induced corneal vascularization. Am J PathoL 1975;81:531–544.
   PubMed Web of Science ®Google Scholar
• Ormerod LD, Abelson MB, Kenyon KR. Standard models of corneal injury using alkali-immersed filter discs. Invest Ophthalmol Vis Sci. 1989;30:2148–2153.
   PubMed Web of Science ®Google Scholar