N-Acetyl-L-cysteine Protects Human Retinal Pigment Epithelial Cells from Oxidative Damage: Implications for Age-Related Macular Degeneration

المؤلفون المشاركون

Ferrington, Deborah A.
Terluk, Marcia R.
Ebeling, Mara C.
Fisher, Cody R.
Kapphahn, Rebecca J.
Yuan, Ching
Kartha, Reena V.
Montezuma, Sandra R.

المصدر

Oxidative Medicine and Cellular Longevity

العدد

المجلد 2019، العدد 2019 (31 ديسمبر/كانون الأول 2019)، ص ص. 1-14، 14ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2019-08-14

دولة النشر

مصر

عدد الصفحات

14

التخصصات الرئيسية

الأحياء

الملخص EN

Age-related macular degeneration (AMD) involves the loss of retinal pigment epithelium (RPE) and photoreceptors and is one of the leading causes of blindness in the elderly.

Oxidative damage to proteins, lipids, and DNA has been associated with RPE dysfunction and AMD.

In this study, we evaluated oxidative stress in AMD and the efficacy of antioxidant, N-acetyl-L-cysteine (NAC), in protecting RPE from oxidative damage.

To test this idea, primary cultures of RPE from human donors with AMD (n=32) or without AMD (No AMD, n=21) were examined for expression of NADPH oxidase (NOX) genes, a source of reactive oxygen species (ROS).

Additionally, the cells were pretreated with NAC for 2 hours and then treated with either hydrogen peroxide (H2O2) or tert-butyl hydroperoxide (t-BHP) to induce cellular oxidation.

Twenty-four hours after treatment, ROS production, cell survival, the content of glutathione (GSH) and adenosine triphosphate (ATP), and cellular bioenergetics were measured.

We found increased expression of p22phox, a NOX regulator, in AMD cells compared to No AMD cells (p=0.02).

In both AMD and No AMD cells, NAC pretreatment reduced t-BHP-induced ROS production and protected from H2O2-induced cell death and ATP depletion.

In the absence of oxidation, NAC treatment improved mitochondrial function in both groups (p<0.01).

Conversely, the protective response exhibited by NAC was disease-dependent for some parameters.

In the absence of oxidation, NAC significantly reduced ROS production (p<0.001) and increased GSH content (p=0.02) only in RPE from AMD donors.

Additionally, NAC-mediated protection from H2O2-induced GSH depletion (p=0.04) and mitochondrial dysfunction (p<0.05) was more pronounced in AMD cells compared with No AMD cells.

These results demonstrate the therapeutic benefit of NAC by mitigating oxidative damage in RPE.

Additionally, the favorable outcomes observed for AMD RPE support NAC’s relevance and the potential therapeutic value in treating AMD.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Terluk, Marcia R.& Ebeling, Mara C.& Fisher, Cody R.& Kapphahn, Rebecca J.& Yuan, Ching& Kartha, Reena V.…[et al.]. 2019. N-Acetyl-L-cysteine Protects Human Retinal Pigment Epithelial Cells from Oxidative Damage: Implications for Age-Related Macular Degeneration. Oxidative Medicine and Cellular Longevity،Vol. 2019, no. 2019, pp.1-14.
https://search.emarefa.net/detail/BIM-1204016

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Terluk, Marcia R.…[et al.]. N-Acetyl-L-cysteine Protects Human Retinal Pigment Epithelial Cells from Oxidative Damage: Implications for Age-Related Macular Degeneration. Oxidative Medicine and Cellular Longevity No. 2019 (2019), pp.1-14.
https://search.emarefa.net/detail/BIM-1204016

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Terluk, Marcia R.& Ebeling, Mara C.& Fisher, Cody R.& Kapphahn, Rebecca J.& Yuan, Ching& Kartha, Reena V.…[et al.]. N-Acetyl-L-cysteine Protects Human Retinal Pigment Epithelial Cells from Oxidative Damage: Implications for Age-Related Macular Degeneration. Oxidative Medicine and Cellular Longevity. 2019. Vol. 2019, no. 2019, pp.1-14.
https://search.emarefa.net/detail/BIM-1204016

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1204016