Lee A Y, Chung S S
Institute of Molecular Biology, University of Hong Kong, Pokfulam.
Invest Ophthalmol Vis Sci. 1998 Jan;39(1):193-7.
The authors investigated the involvement of the enzyme aldose reductase (AR) in naphthalene cataract by using transgenic mice that overexpress AR.
Lenses from nontransgenic mice and from transgenic lines CAR222 and CAR648, with different levels of AR, were cultured in medium containing naphthalene-1,2-dihydrodiol (ND) with or without AR inhibitor AL1576. The morphology and progression rate of ND-induced cataract in these lenses were compared.
Lenses from transgenic mice CAR222 and CAR648, but not their nontransgenic littermates, developed yellow pigment in the inner cortex when exposed to 50 microM ND, which was completely prevented by 0.2 mM AL1576. The yellow pigment developed faster and more intensely in the CAR648 lens, which has a higher AR level than CAR222. Under a high dose of 500 microM ND, both transgenic and wild-type mouse lenses developed ND-induced cataract, although the first sign of cataract was found in the outer cortex in transgenic lenses instead of the inner cortical region in wild-type lenses. In addition, the cataract was more severe and developed at a faster rate in transgenic mouse lenses. AL1576 showed only partial protection against the cataract induced by 500 microM ND.
The findings showed that the progression rate of ND-induced cataract correlated with the level of lens AR and ND, indicating that AR was the key enzyme for the metabolism of ND in the process of naphthalene cataract development.
作者通过使用过表达醛糖还原酶(AR)的转基因小鼠,研究了AR在萘性白内障中的作用。
将来自非转基因小鼠以及AR水平不同的转基因品系CAR222和CAR648的晶状体,在含有萘-1,2-二氢二醇(ND)且添加或不添加AR抑制剂AL1576的培养基中培养。比较这些晶状体中ND诱导的白内障的形态和进展速率。
当暴露于50微摩尔/升的ND时,转基因小鼠CAR222和CAR648的晶状体,而非其非转基因同窝小鼠的晶状体,在内皮层出现黄色色素,0.2毫摩尔/升的AL1576可完全阻止这种情况。黄色色素在CAR648晶状体中形成得更快且更强烈,其AR水平高于CAR222。在500微摩尔/升的高剂量ND作用下,转基因和野生型小鼠晶状体均出现ND诱导的白内障,尽管转基因晶状体中白内障的首个迹象出现在外皮层,而野生型晶状体中出现在内皮层区域。此外,转基因小鼠晶状体中的白内障更严重且进展更快。AL1576对500微摩尔/升ND诱导的白内障仅显示出部分保护作用。
研究结果表明,ND诱导的白内障的进展速率与晶状体AR水平和ND相关,表明AR是萘性白内障发展过程中ND代谢的关键酶。