Sasaki H, Giblin F J, Winkler B S, Chakrapani B, Leverenz V, Shu C C
Eye Research Institute, Oakland University, Rochester, Michigan 48309-4401, USA.
Invest Ophthalmol Vis Sci. 1995 Aug;36(9):1804-17.
In view of the antioxidant role of ascorbic acid and the glutathione redox cycle in the lens, the authors have studied the relationship of the cycle to reduction of the oxidized product of ascorbic acid, dehydroascorbic acid (DHA), in lens epithelium.
Cultured dog lens epithelial cells and intact rabbit lenses were exposed to various concentrations of DHA in experiments performed at 20 degrees C to minimize hydrolysis of the compound (t1/2 of 5 minutes at 37 degrees C). Levels of glutathione (GSH) and oxidized glutathione (GSSG) were measured in lens cells and whole lens epithelial by electrochemical detection.
Treatment of lens cells with 1 mM DHA for 0.5 to 3 hours in the absence of glucose (glucose is required for the reduction of GSSG through the glutathione redox cycle) produced from 60% to complete oxidation of GSH (controls contained negligible GSSG) and distinct morphologic changes (cell contraction and blebbing), as shown by scanning electron microscopy. Glucose prevented these effects and allowed nearly immediate recovery of GSH after DHA exposure in the absence of glucose. A dose-dependent response was observed for the formation of GSSG in cultured cells from 0.05 to 0.5 mM DHA in the absence of glucose. The results of experiments performed with DHA plus an inhibitor of glutathione reductase mimicked those obtained using DHA minus glucose. DHA produced a 3- to 10-fold stimulation of hexose monophosphate shunt activity in cultured lens cells and whole lenses, which was prevented by the inhibition of glutathione reductase. Treatment of whole lenses with DHA minus glucose also produced oxidation of epithelial GSH and was accompanied by the loss of lens transparency. No evidence was found for dehydroascorbate reductase activity in the lens epithelium.
The exposure of lenses and lens epithelial cells to DHA under conditions in which the glutathione redox cycle was compromised resulted in the disappearance of GSH in the tissues and the appearance of GSSG. The reduction of DHA was shown to be linked to the glutathione redox cycle by a nonenzymatic interaction between GSH and DHA. Reduction of DHA in the lens is important because of the potential toxicity of this oxidant and/or its degradation products.
鉴于抗坏血酸和谷胱甘肽氧化还原循环在晶状体中的抗氧化作用,作者研究了该循环与晶状体上皮中抗坏血酸氧化产物脱氢抗坏血酸(DHA)还原之间的关系。
在20℃进行实验,以使化合物水解最小化(37℃时半衰期为5分钟),将培养的犬晶状体上皮细胞和完整的兔晶状体暴露于不同浓度的DHA中。通过电化学检测测量晶状体细胞和整个晶状体上皮中的谷胱甘肽(GSH)和氧化型谷胱甘肽(GSSG)水平。
在无葡萄糖的情况下(通过谷胱甘肽氧化还原循环还原GSSG需要葡萄糖),用1 mM DHA处理晶状体细胞0.5至3小时,导致GSH氧化60%至完全氧化(对照组GSSG含量可忽略不计),并出现明显的形态学变化(细胞收缩和起泡),扫描电子显微镜显示。葡萄糖可防止这些影响,并在无葡萄糖的情况下DHA暴露后使GSH几乎立即恢复。在无葡萄糖的情况下,观察到培养细胞中从0.05至0.5 mM DHA形成GSSG呈剂量依赖性反应。用DHA加谷胱甘肽还原酶抑制剂进行的实验结果与用DHA减葡萄糖获得的结果相似。DHA在培养的晶状体细胞和整个晶状体中对磷酸己糖旁路活性产生3至10倍的刺激,这可通过抑制谷胱甘肽还原酶来防止。用DHA减葡萄糖处理整个晶状体也会导致上皮GSH氧化,并伴有晶状体透明度丧失。在晶状体上皮中未发现脱氢抗坏血酸还原酶活性的证据。
在谷胱甘肽氧化还原循环受损的条件下,将晶状体和晶状体上皮细胞暴露于DHA会导致组织中GSH消失和GSSG出现。DHA的还原被证明通过GSH和DHA之间的非酶相互作用与谷胱甘肽氧化还原循环相关。晶状体中DHA的还原很重要,因为这种氧化剂和/或其降解产物具有潜在毒性。