2005
DOI: 10.1016/j.jphotobiol.2004.09.005
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Pirenoxine prevents oxidative effects of argon fluoride excimer laser irradiation in rabbit corneas: biochemical, histological and cytofluorimetric evaluations

Abstract: The production of reactive oxygen species (ROS) associated with excimer laser irradiation is recognized as a possible cause of corneal haze following photorefractive keratectomy (PRK). Our work was aimed at investigating in vitro the oxidative effects induced by subablative laser fluences and at demonstrating the protective effectiveness of pirenoxine. Comparative trials of subablative fluence on rabbit eyes with or without 10 À5 M pirenoxine were carried out. Superoxide anion ðO ÀÅ 2 Þ, conjugated diene (CD),… Show more

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Cited by 9 publications
(10 citation statements)
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References 34 publications
(38 reference statements)
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“…Reactive species‐mediated cellular damage instigates lipid peroxidation and apoptosis throughout the cornea . Moreover, the detachment of epithelial cells from one another and their basement membrane in addition to alterations to the thickness of the epithelial layer may disrupt the integrity of this permeability barrier . Nuclear fragmentation is perceptible and mitochondrial DNA damage may diminish mitochondrial and subsequently cell viability by lowering the efficiency of oxidative phosphorylation, intensifying reactive oxygen species formation .…”
Section: Reactive Species Antioxidants and Oxidative Stress In The Nmentioning
confidence: 99%
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“…Reactive species‐mediated cellular damage instigates lipid peroxidation and apoptosis throughout the cornea . Moreover, the detachment of epithelial cells from one another and their basement membrane in addition to alterations to the thickness of the epithelial layer may disrupt the integrity of this permeability barrier . Nuclear fragmentation is perceptible and mitochondrial DNA damage may diminish mitochondrial and subsequently cell viability by lowering the efficiency of oxidative phosphorylation, intensifying reactive oxygen species formation .…”
Section: Reactive Species Antioxidants and Oxidative Stress In The Nmentioning
confidence: 99%
“…95,[99][100][101][102] Moreover, the detachment of epithelial cells from one another and their basement membrane in addition to alterations to the thickness of the epithelial layer may disrupt the integrity of this permeability barrier. 83,103,104 Nuclear fragmentation is perceptible and mitochondrial DNA damage may diminish mitochondrial and subsequently cell viability by lowering the efficiency of oxidative phosphorylation, intensifying reactive oxygen species formation. [104][105][106] Stromal scarring manifests from a reparative response and causes haze from light scattering, 107,108 while covalent bonding disruptions in stromal matrix collagen and proteoglycan molecules may precede disorganisation and aggregation of the collagen fibres.…”
Section: Oxidative Stress and The Effects Of Antioxidantsmentioning
confidence: 99%
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“…After liquid-phase separation (centrifugation at 2000 g for 10 min), the absorbance of the pink organic phase was spectrophotometrically evaluated at 532 nm and TBARS was expressed as nmoles of malondialdehyde (MDA)/10 mg of rat brain tissue (wet weight), using a curve with 1,1,3,3-tetramethoxypropane as the standard reference. 54 Computational Chemistry. Molecular modeling and graphics manipulations were performed using the SYBYL 55 and UCSF CHIMERA software packages, 56 running them on a Silicon Graphics Tezro R16000 workstation.…”
Section: General Procedures For the Synthesis Of 2-phenylpyrido[12-a]mentioning
confidence: 99%
“…Известно, что противокатарактальное действие пиреноксина включает в себя следующие основные механизмы: ингибирование действия хиноновых соединений (продуктов нарушенного метаболизма ароматических аминокислот в хрусталике) и замедление процесса денатурации (перехода растворимого белка хрусталика в нерастворимую форму); нормализацию обмена глюкозы в хрусталике и препятствие отложению сорбита; стабилизацию клеточных мембран [9][10][11][12]. Кроме того, ряд публикаций указывает на антиоксидантные свойства пиреноксина, связанные с его способностью ингибировать перекисное окисление липидов (в том числе в хрусталике млекопитающих), что обусловливает возможность его использования для профилактики катарактогенеза у пациентов после витрэктомии [11,12]. Вышеуказанные исследования проводились на лабораторных животных, однако в доступной научной литературе нам не удалось обнаружить данные о возможности использования пиреноксина в профилактике развития катаракты у пациентов после витрэктомии и удаления ЭРМ.…”
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