The seeds of () species mainly contain anthraquinone, anthraquinone glycoside, and naphthalene derivatives. We investigated the anti-apoptotic effects of seed extract and its isolated compounds on blue-light-induced lipofuscin (A2E)-loaded human retinal pigment epithelial (RPE) cells. For analysis of the extract, high-performance liquid chromatography method was used. A2E-loaded human retinal pigment epithelial cells and blue light were used to create excessive photo-oxidation to induce cell death. Lactate dehydrogenase (LDH) assay was used to measure cell cytotoxicity, and the mRNA expression of genes involved in apoptosis was examined to evaluate the mechanism of cell death. extract, -hexane fraction, and chrysophanol were found to inhibit apoptotic cell death. Additionally, extract, -hexane fraction, and chrysophanol reduced the mRNA expression of genes involved in the apoptosis pathway. and chrysophanol were considered to inhibit apoptosis and oxidative stress response. The major component of has a protective effect against apoptosis. The ingredients of can be used as therapeutic substances or to prevent diseases caused by the excessive oxidation of A2E substances in the retina, such as in age-related macular degeneration.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095300PMC
http://dx.doi.org/10.3390/ijms24076676DOI Listing

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Article Synopsis
  • - The study investigates the role of oxidative stress and unknown phototoxicity mechanisms in age-related macular degeneration (AMD), focusing on inhibiting the harmful aggregation of a key fluorophore, A2E.
  • - Using a drug repurposing approach, researchers identified entacapone as an effective inhibitor of A2E fluorescence and aggregation, which helps protect retinal cells from blue light damage.
  • - Entacapone appears to redirect A2E into less harmful forms, showing that the aggregation of A2E contributes to its phototoxic effects, offering potential therapeutic insights for AMD treatment.
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The seeds of () species mainly contain anthraquinone, anthraquinone glycoside, and naphthalene derivatives. We investigated the anti-apoptotic effects of seed extract and its isolated compounds on blue-light-induced lipofuscin (A2E)-loaded human retinal pigment epithelial (RPE) cells. For analysis of the extract, high-performance liquid chromatography method was used.

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Aims: In a model of blue light-induced damage in N-retinylidene-N-retinylethanolamine (A2E)-loaded human retinal pigment epithelial (RPE) cells, we examined the effect of A2E on the calcium (Ca)-protein kinase C (PKC) signaling pathway.

Methods: Primary human RPE cells were cultured, and the cells in the 4th-6th passages were used in this study. The cells were divided into 5 groups: control cells (no A2E, no blue light), blue light-treated cells, blue light + chloroquine-treated cells, blue light + A2E-treated cells, and blue light + A2E + chloroquine-treated cells.

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Background: To investigate the effect of N-retinyl-N-retinylidene ethanolamine (A2E) on lysosome membrane permeability (LMP) during blue light-induced human retinal pigment epithelium cells (RPEs) apoptosis.

Methods: By building an A2E and blue light irradiation inducing RPEs damage model, the CCK-8 assay was used to detect RPEs viability loaded with different concentrations of A2E after different culturing time to determine the optimum A2E loading concentration. And the RPEs fluorescence intensity changes were observed by fluorescence microscopy loaded with different concentration of A2E.

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Lighting is rapidly changing with the introduction of light-emitting diodes (LEDs) in our homes, workplaces, and cities. This evolution of our optical landscape raises major concerns regarding phototoxicity to the retina since light exposure is an identified risk factor for the development of age-related macular degeneration (AMD). In this disease, cone photoreceptors degenerate while the retinal pigment epithelium (RPE) is accumulating lipofuscin containing phototoxic compounds such as A2E.

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