ENHANCEMENT OF FILTRATION SURGERY WITH CYTOSINE-ARABINOSIDE AND REVERSAL OF TOXICITY WITH 2'-DEOXYCYTIDINE

Citation
Jl. Chu et al., ENHANCEMENT OF FILTRATION SURGERY WITH CYTOSINE-ARABINOSIDE AND REVERSAL OF TOXICITY WITH 2'-DEOXYCYTIDINE, Current eye research, 13(11), 1994, pp. 839-843
Citations number
28
Categorie Soggetti
Ophthalmology
Journal title
ISSN journal
02713683
Volume
13
Issue
11
Year of publication
1994
Pages
839 - 843
Database
ISI
SICI code
0271-3683(1994)13:11<839:EOFSWC>2.0.ZU;2-0
Abstract
Antifibrosis agents have improved the success of glaucoma filtration s urgery, although undesired side effects are not readily reversible and may present a major limitation in the use of these agents. Our purpos e was to study the efficacy of cytosine arabinoside (Ara-C) as an adju nctive antimetabolite in glaucoma surgery in the rabbit, and reversal of toxicity due to this agent with the competitive inhibitor 2'-deoxyc ytidine. Posterior lip sclerectomy was performed in rabbit eyes treate d with 15 mg subconjunctival Ara-C daily for 7 d then every other day for 7 d. Mean intraocular pressure was lower in eyes treated with Ara- C compared with controls at all time points following filtration surge ry. On the 10th postoperative day, the mean intraocular pressure of co ntrol eyes (25.0 +/- 1.9 mm Hg) had returned to baseline levels, where as the intraocular pressure of eyes treated with Ara-C was significant ly lower (16.0 +/- 1.7 mm Hg) (P < 0.01). Bleb survival was also prolo nged in the Ara-C-treated eyes. The major ocular side effect of Ara-C was corneal toxicity, with epithelial defects in 40% of eyes after 8 d aily injections of 15 mg Ara-C. Reversal of toxicity was enhanced with 2'-deoxycytidine, with complete resolution of epithelial toxicity aft er 6.5 +/- 1.7 d following daily topical 10% 2'-deoxycytidine compared with 12.7 +/- 0.58 for control (P < 0.002). These results demonstate that postoperative subconjunctival injection of Ara-C results in impro ved bleb function after filtration surgery in the rabbit. Recovery fro m corneal epithelial toxicity due to Ara-C is markedly enhanced with t he competitive inhibitor 2'-deoxycytidine.