首页> 外文期刊>Fundamental & clinical pharmacology. >Telomere-dependent senescent phenotype of lens epithelial cells as a biological marker of aging and cataractogenesis: the role of oxidative stress intensity and specific mechanism of phospholipid hydroperoxide toxicity in lens and aqueous.
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Telomere-dependent senescent phenotype of lens epithelial cells as a biological marker of aging and cataractogenesis: the role of oxidative stress intensity and specific mechanism of phospholipid hydroperoxide toxicity in lens and aqueous.

机译:晶状体上皮细胞端粒依赖性衰老表型是衰老和白内障发生的生物学标志:晶状体和眼房水中氧化应激强度的作用和磷脂氢过氧化物毒性的特定机制。

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摘要

Cataract formation represents a serious problem in the elderly and has a large impact on healthcare budget. Aging and cataract formation are relatively complex phenomena, both in vivo and in vitro. Telomeres are special structures at the end of chromosomes. They shorten during each round of replication, and this has been characterized as a mitotic counting mechanism. Our review analysis in this work shows that the rate of telomere shortening in human lens epithelial cells during aging and cataract formation is modulated by oxidative stress as well as by differences in antioxidative defense capacity of the normal and cataractous crystalline lenses. Presented in this review studies suggest that telomere shortening in human lens cells and increased oxidative stress are the result of the peroxidative damage to the lens cell membranes and biomolecules induced in the lack of reductive detoxification of phospholipid hydroperoxides as the triggering mechanism of cataractogenesis. Lipid peroxidation (LPO) is a causative factor of cataract. The increased concentrations of primary molecular LPO products (diene conjugates, lipid hydroperoxides) and end fluorescent LPO products were detected in the lipid moieties of the aqueous humor samples obtained from patients with senile and complicated cataracts when compared to normal donors. The progressive accumulation of oxidative damage may act as an important mechanism for organism aging and cataractogenesis. The oxidative stress form and intensity might determine the lens senescence rate and cataract type, making efforts in the cataract prevention challenge more complex. The analyzed challenge in this work is that the reduction in telomere shortening rate and damages in telomeric DNA make an important contribution to the anticataract and life-extension effect of carnosine administered systemically in the formulations stabilizing a dipeptide from the enzymatic hydrolysis with carnosinase, or topically administered to the eye with carnosine ophthalmic prodrug N-acetylcarnosine and lubricant formulations thereof including corneal absorption promoters. Telomere length in the human crystalline lens cells is a reflection of aging, cataractogenesis, and lifespan in biogerontological studies.
机译:白内障形成是老年人的一个严重问题,对医疗保健预算有很大影响。在体内和体外,衰老和白内障形成都是相对复杂的现象。端粒是染色体末端的特殊结构。它们在每一轮复制过程中都会缩短,这被称为有丝分裂计数机制。我们在这项工作中的回顾分析表明,在老化和白内障形成过程中,人晶状体上皮细胞端粒缩短的速率受氧化应激以及正常和白内障晶状体抗氧化防御能力的差异调节。在这篇综述中提出的研究表明,人晶状体细胞中端粒的缩短和氧化应激的增加是由于缺乏晶状体白内障的触发机制的磷脂氢过氧化物的还原性解毒而引起的对晶状体细胞膜和生物分子的过氧化损伤的结果。脂质过氧化(LPO)是白内障的病因。与正常供体相比,从患有老年和复杂性白内障患者获得的房水样本的脂质部分中检测到初级分子LPO产物(二烯共轭物,脂质氢过氧化物)和末端荧光LPO产物的浓度增加。氧化损伤的逐步积累可能是机体衰老和白内障发生的重要机制。氧化应激的形式和强度可能决定晶状体的衰老率和白内障类型,使预防白内障的工作更加复杂。在这项工作中分析的挑战是端粒缩短速率的降低和端粒DNA的损伤为肌肽的全身性给药提供了重要的贡献,肌肽的作用是稳定肌肽酶酶促水解过程中的二肽,或者局部给药与肌肽眼药前药N-乙酰肌肽及其包括角膜吸收促进剂的润滑剂制剂一起给予眼睛。人晶状体细胞中端粒的长度反映了生物老年学研究中的衰老,白内障发生和寿命。

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