Good P A, Claxson A, Morris C J, Blake D R
Birmingham and Midland Eye Hospital, UK.
Ophthalmologica. 1990;201(1):32-6. doi: 10.1159/000310122.
We describe a rat model of the ocular toxicity induced in patients by the iron chelator desferrioxamine (DFX). The functional integrity of the rat photoreceptor membrane is assessed by measurement of the electroretinogram b wave amplitude. Following single bolus doses of DFX (50, 100 and 150 mg), rats develop dose-related suppression of b wave amplitude within 48 h. Recovery takes place over the subsequent 14 days. This ocular damage is exacerbated by exposure to increased levels of white light and oxygen. Studies in this model also show that darkness and, in particular, red light protect the eye against DFX toxicity. This is of potential use in patient management during DFX therapy.
我们描述了一种由铁螯合剂去铁胺(DFX)在患者中诱发的眼部毒性大鼠模型。通过测量视网膜电图b波振幅来评估大鼠光感受器膜的功能完整性。单次推注DFX(50、100和150毫克)后,大鼠在48小时内出现与剂量相关的b波振幅抑制。在随后的14天内恢复。暴露于增加的白光和氧气水平会加剧这种眼部损伤。该模型的研究还表明,黑暗,尤其是红光可保护眼睛免受DFX毒性的影响。这在DFX治疗期间的患者管理中具有潜在用途。