Barker F M, Dayhaw-Barker P, Forbes P D, Davies R E
Acta Ophthalmol (Copenh). 1986 Aug;64(4):471-8. doi: 10.1111/j.1755-3768.1986.tb06955.x.
Hairless (HRA/Skh) mice were administered one of four dietary concentrations (50, 100, 625 or 1250 ppm) of 8-methoxypsoralen (8-MOP) or 5-methoxypsoralen (5-MOP), or molar equivalent concentrations of 5-methylisopsoralen (5-MIP) or 3-carbethoxypsoralen (3-CPS) by 'pulse feeding' technique, 3 days per week for 13 weeks. For the final 11 weeks psoralen derivative administration was followed by exposure to 0.2 or 48 J/cm2 of unfiltered ultraviolet-A (UVA) radiant energy from FR74T12PUVA lamps. At 0 and 13 weeks eyes were dilated with 0.2% atropine solution and were examined using a binocular indirect ophthalmoscope with a +20.0 D condensing lens. The lids, cornea, anterior chamber and the lens were evaluated for pathological changes. Ocular damage consisting of dense central corneal opacification was seen at significant levels in animals given 8-MOP or 5-MOP and exposed to UVA. In addition, opacities in the area of the posterior lens were seen in all experimental groups and appeared to be related to drug treatment, independent of light exposure, and therefore appeared not to be related to drug-light interaction. Some corneal and lenticular opacification was seen at non-significant levels in all experimental and control groups.
通过“脉冲喂食”技术,每周3天,持续13周,给无毛(HRA/Skh)小鼠喂食四种饮食浓度(50、100、625或1250 ppm)的8-甲氧基补骨脂素(8-MOP)或5-甲氧基补骨脂素(5-MOP),或摩尔当量浓度的5-甲基异补骨脂素(5-MIP)或3-乙氧羰基补骨脂素(3-CPS)。在最后11周,给予补骨脂素衍生物后,让小鼠暴露于FR74T12PUVA灯发出的0.2或48 J/cm²未过滤的紫外线A(UVA)辐射能量下。在第0周和第13周,用0.2%阿托品溶液散瞳,并用带有+20.0 D聚光镜的双目间接检眼镜进行检查。评估眼睑、角膜、前房和晶状体的病理变化。在给予8-MOP或5-MOP并暴露于UVA的动物中,观察到显著水平的由致密中央角膜混浊组成的眼部损伤。此外,在所有实验组中均观察到晶状体后区的混浊,并且似乎与药物治疗有关,与光照无关,因此似乎与药物-光相互作用无关。在所有实验组和对照组中均观察到一些非显著水平的角膜和晶状体混浊。