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高压氧治疗的老年豚鼠晶状体中的核光散射、二硫键形成及膜损伤

Nuclear light scattering, disulfide formation and membrane damage in lenses of older guinea pigs treated with hyperbaric oxygen.

作者信息

Giblin F J, Padgaonkar V A, Leverenz V R, Lin L R, Lou M F, Unakar N J, Dang L, Dickerson J E, Reddy V N

机构信息

Eye Research Institute, Oakland University Rochester, MI 48309-4401, USA.

出版信息

Exp Eye Res. 1995 Mar;60(3):219-35. doi: 10.1016/s0014-4835(05)80105-8.

DOI:10.1016/s0014-4835(05)80105-8
PMID:7789403
Abstract

Nuclear cataract, a major cause of loss of lens transparency in the aging human, has long been thought to be associated with oxidative damage, particularly at the site of the nuclear plasma membrane. However, few animal models have been available to study the mechanism of the opacity. Hyperbaric oxygen (HBO) has been shown to produce increased nuclear light scattering (NLS) and nuclear cataract in lenses of mice and human patients. In the present study, older guinea pigs (Initially 17-18 months of age) were treated with 2.5 atmospheres of 100% O2 for 2-2.5-hr periods, three times per week, for up to 100 times. Examination by slit-lamp biomicroscopy showed that exposure to HBO led to increased NLS in the lenses of the animals after as few as 19 treatments, compared to lenses of age-matched untreated and hyperbaric air-treated controls. The degree of NLS and enlargement of the lens nucleus continued to increase until 65 O2-treatments, and then remained constant until the end of the study. Exposure to O2 for 2.5 instead of 2 hr accelerated the increase in NLS; however, distinct nuclear cataract was not observed in the animals during the period of investigation. A number of morphological changes in the experimental lens nuclei, as analysed by transmission electron microscopy, were similar to those recently reported for human immature nuclear cataracts (Costello, Oliver and Cobo, 1992). O2-induced damage to membranes probably acted as scattering centers and caused the observed increased NLS. A general state of oxidative stress existed in the lens nucleus of the O2-treated animals, prior to the first appearance of increased NLS, as evidenced by increased levels of protein-thiol mixed disulfides and protein disulfide. The levels of mixed disulfides in the experimental nucleus were remarkably high, nearly equal to the normal level of nuclear GSH. The level of GSH in the normal guinea pig lens decreased with age in the nucleus but not in the cortex; at 30 months of age the nuclear level of GSH was only 4% of the cortical value. HBO-induced changes in the lens nucleus included loss of soluble protein, increase in urea-insoluble protein and slight decreases in levels of GSH and ascorbate; however, there was no accumulation of oxidized glutathione. Intermolecular protein disulfide in the experimental nucleus consisted mainly of gamma-crystallin, but crosslinked alpha-, beta- and zeta-crystallins were also present.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

核性白内障是老年人晶状体透明度丧失的主要原因,长期以来一直被认为与氧化损伤有关,尤其是在核质膜部位。然而,很少有动物模型可用于研究其混浊机制。高压氧(HBO)已被证明会使小鼠和人类患者晶状体的核光散射(NLS)增加并导致核性白内障。在本研究中,对年龄较大的豚鼠(初始年龄为17 - 18个月)进行治疗,让其在2.5个大气压的100%氧气环境中暴露2 - 2.5小时,每周3次,最多进行100次。裂隙灯生物显微镜检查显示,与年龄匹配的未治疗和高压空气治疗的对照组晶状体相比,仅经过19次治疗后,暴露于HBO的动物晶状体中的NLS就增加了。NLS的程度和晶状体核的增大一直持续增加,直到65次氧气治疗,然后在研究结束前保持稳定。暴露于氧气2.5小时而非2小时会加速NLS的增加;然而,在研究期间未在动物中观察到明显的核性白内障。通过透射电子显微镜分析,实验性晶状体核中的一些形态学变化与最近报道的人类未成熟核性白内障的变化相似(科斯特洛、奥利弗和科博,1992年)。氧气诱导的膜损伤可能充当散射中心并导致观察到的NLS增加。在NLS首次增加之前,经氧气处理的动物晶状体核中就存在氧化应激的总体状态,蛋白质 - 硫醇混合二硫化物和蛋白质二硫化物水平的增加证明了这一点。实验性晶状体核中的混合二硫化物水平非常高,几乎与核内谷胱甘肽(GSH)的正常水平相等。正常豚鼠晶状体中GSH的水平在核内随年龄下降,但在皮质中不下降;在30个月大时,核内GSH水平仅为皮质值的4%。HBO诱导晶状体核的变化包括可溶性蛋白质的丧失以及尿素不溶性蛋白质的增加,GSH和抗坏血酸水平略有下降;然而,没有氧化型谷胱甘肽的积累。实验性晶状体核中的分子间蛋白质二硫化物主要由γ - 晶状体蛋白组成,但也存在交联的α -、β - 和ζ - 晶状体蛋白。(摘要截选至400字)

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