Varma S D, Chand D, Sharma Y R, Kuck J F, Richards R D
Curr Eye Res. 1984 Jan;3(1):35-57. doi: 10.3109/02713688408997186.
The mechanism of oxidative damage to the lens through intraocular photochemical generation of superoxide and its derivatization to other oxidants such as singlet oxygen, hydroxyl radical and hydrogen peroxide has been studied. Rat lenses when organ cultured aerobically in TC 199 containing additional amounts of riboflavin were damaged as demonstrated by an inhibition of the uptake of Rb 86 against a concentration gradient. The pump was not affected by light if the culture was conducted in the basal TC 199. However, light was observed to induce significant peroxidative degradation of the tissue lipids even in the basal medium, the degradation being indicated by the formation of malonaldehyde. Both the inhibition of the pump as well as the peroxidative degradation of the tissue lipids, were attenuated considerably by scavengers of superoxide and hydrogen peroxide. In addition, the lipid degradation was prevented by vitamins C and E. The results suggest that the photodynamic injury to the lens cation pump as well as to membrane lipids is incumbent upon an initial generation of superoxide and its derivatization to other oxidants. Thus, the ocular lens is susceptible to oxidative insult and physiological damage through photocatalytic generation of various oxygen radicals. Large concentrations of ascorbic acid in the aqueous humor seems to be able to provide significant protection against such an insult. Thus, this may be one of the functions of high concentration of ascorbic acid in the aqueous humor. The implication of oxidative stress has also been examined in the genesis of cataracts in vivo. Treatment with vitamin E of the Emory mouse led to a decrease in the rate of cataract progression suggesting that at least in some instances an oxidative stress could participate in the formation of cataracts. Oxygen radicals may inflict damage at multifarious biochemical sites. Human lens lipids were also shown to have an absorption maxima at 239 nm indicating their susceptibility to oxidative degradation. In addition the lipid extract has fluorescence similar to that of lipofuscins. The levels of MDA were higher in the brunescent cataracts as compared to that in the nonbrunescent cataracts. The implications of oxidative stress towards the genesis of cataracts in humans is being explored further.
通过眼内光化学产生超氧化物及其衍生为其他氧化剂(如单线态氧、羟基自由基和过氧化氢)对晶状体造成氧化损伤的机制已得到研究。当在含有额外核黄素的TC 199中进行需氧器官培养时,大鼠晶状体受到损伤,这表现为Rb 86逆浓度梯度摄取受到抑制。如果在基础TC 199中进行培养,泵不受光照影响。然而,即使在基础培养基中,光照也会导致组织脂质发生显著的过氧化降解,丙二醛的形成表明了这种降解。超氧化物和过氧化氢清除剂能显著减轻泵的抑制以及组织脂质的过氧化降解。此外,维生素C和E可防止脂质降解。结果表明,晶状体阳离子泵和膜脂质的光动力损伤依赖于超氧化物的初始产生及其衍生为其他氧化剂。因此,眼晶状体易受各种氧自由基的光催化产生所导致的氧化损伤和生理损害。房水中高浓度的抗坏血酸似乎能够提供显著的保护以抵御这种损伤。因此,这可能是房水中高浓度抗坏血酸的功能之一。氧化应激在体内白内障发生中的影响也已得到研究。用维生素E治疗埃默里小鼠导致白内障进展速率降低,这表明至少在某些情况下,氧化应激可能参与白内障的形成。氧自由基可能在多种生化位点造成损伤。人晶状体脂质在239 nm处也有吸收最大值,表明它们易受氧化降解。此外,脂质提取物具有与脂褐素相似的荧光。与非褐色白内障相比,褐色白内障中丙二醛水平更高。氧化应激对人类白内障发生的影响正在进一步探索。