Costarides A, Recasens J F, Riley M V, Green K
Department of Ophthalmology, Medical College of Georgia, Augusta 30912.
Lens Eye Toxic Res. 1989;6(1-2):167-73.
3-aminotriazole (3-AT), a catalase inhibitor, given to pigmented rabbits in 0.2% drinking solution for 43 days, produced cataractous changes and over a 50% reduction in iris and ciliary process catalase activity. Aqueous H2O2 levels were suppressed by 60% which correlated with a 77% reduction in aqueous ascorbate concentration. Intravenous 3-AT at 1.0 g/kg body weight had no effect on either aqueous ascorbate or H2O2 levels. BCNU (1,3-bis-(2-chloroethyl)-1-nitrosourea) was given intravitreally to rabbits: 3.0 mg suppressed iris glutathione reductase activity by 80%, but only increased the oxidized glutathione/total glutathione ratio to 26% from 18%. Both aqueous ascorbate and H2O2 levels were unaltered at 48 hours. Buthionine sulfoximine (BSO) was given intravitreally; at 48 hours after 4.0 mg BSO, iris-ciliary body total glutathione levels were reduced by 80%, aqueous ascorbate levels were reduced by 53%, and aqueous H2O2 levels were unaltered. A direct correlation seems to exist between aqueous humor ascorbate and H2O2 concentrations, even during suppression of tissue catalase activity. Changes in glutathione status cause peroxide levels to be greater than predicted from the aqueous ascorbate concentration.
3-氨基三唑(3-AT)是一种过氧化氢酶抑制剂,以0.2%的溶液形式给予有色家兔饮用43天,会导致白内障变化,并使虹膜和睫状体的过氧化氢酶活性降低超过50%。房水过氧化氢水平被抑制了60%,这与房水抗坏血酸浓度降低77%相关。静脉注射1.0 g/kg体重的3-AT对房水抗坏血酸或过氧化氢水平均无影响。将卡莫司汀(1,3-双(2-氯乙基)-1-亚硝基脲)玻璃体内注射到家兔体内:3.0 mg可使虹膜谷胱甘肽还原酶活性降低80%,但仅使氧化型谷胱甘肽/总谷胱甘肽比值从18%增加到26%。48小时时房水抗坏血酸和过氧化氢水平均未改变。丁硫氨酸亚砜胺(BSO)被玻璃体内注射;4.0 mg BSO注射48小时后,虹膜-睫状体总谷胱甘肽水平降低80%,房水抗坏血酸水平降低53%,而房水过氧化氢水平未改变。即使在组织过氧化氢酶活性受到抑制期间,房水抗坏血酸和过氧化氢浓度之间似乎也存在直接相关性。谷胱甘肽状态的变化导致过氧化物水平高于根据房水抗坏血酸浓度预测的水平。