Nguyen K P, Chung M L, Anderson P J, Johnson M, Epstein D L
Howe Laboratory of Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston 02114.
Invest Ophthalmol Vis Sci. 1988 Jun;29(6):976-81.
Previous studies have shown that aqueous humor of calf and human eyes contains about 25 microM hydrogen peroxide. We have studied the removal of hydrogen peroxide by the outflow pathway of intact, freshly enucleated, calf eyes. Eyes were immersed under silicone oil that had a density greater than water and medium containing various agents was perfused into the anterior chamber. Medium passing through the trabecular meshwork and out the cut ends of the aqueous veins was trapped by the silicone oil and harvested. By measuring the concentration of hydrogen peroxide in the anterior chamber and in the emerging medium, we were able to study the rate of removal by the outflow structures and the effect of inhibitors on this rate. At 1 mM hydrogen peroxide, the amount emerging was undetectable by our methods. At 10 mM, the results were inconsistent, suggesting that tissue damage may have been occurring. At 5 mM, the concentration in the emerging medium was reduced 150-1000-fold, depending on time and conditions. This rate of removal could be reduced by 3-aminotriazole, reaching a maximum inhibition of about 50% at 80 mM. Addition of 1,3-bis-(2-chloroethyl)-1-nitrosourea (BCNU) to further inhibit removal did not yield reliable results unless the concentration of H2O2 was lowered below 5 mM. Using loss of lactate dehydrogenase activity as a measure of cell damage, we found a 30% drop in activity after perfusing with BCNU, diamide, and 3-aminotriazole, followed by 3 hr with 10 mM hydrogen peroxide.(ABSTRACT TRUNCATED AT 250 WORDS)
先前的研究表明,小牛和人眼的房水中含有约25微摩尔的过氧化氢。我们研究了完整的、刚摘除的小牛眼的流出途径对过氧化氢的清除作用。将眼睛浸入密度大于水的硅油下,将含有各种试剂的培养基灌注到前房。通过小梁网并从房水静脉的切断端流出的培养基被硅油捕获并收集。通过测量前房和流出培养基中过氧化氢的浓度,我们能够研究流出结构的清除速率以及抑制剂对该速率的影响。在1毫摩尔过氧化氢时,我们的方法检测不到流出的量。在10毫摩尔时,结果不一致,表明可能发生了组织损伤。在5毫摩尔时,流出培养基中的浓度降低了150 - 1000倍,这取决于时间和条件。这种清除速率可被3 - 氨基三唑降低,在80毫摩尔时最大抑制率约为50%。添加1,3 - 双(2 - 氯乙基)-1 - 亚硝基脲(BCNU)以进一步抑制清除,除非过氧化氢浓度降至5毫摩尔以下,否则不会产生可靠结果。以乳酸脱氢酶活性的丧失作为细胞损伤的指标,我们发现在用BCNU、二酰胺和3 - 氨基三唑灌注后,活性下降了30%,随后用10毫摩尔过氧化氢处理3小时。(摘要截短于250字)