dc.contributor.author |
Sahin, K |
|
dc.contributor.author |
Akdemir, F |
|
dc.contributor.author |
Orhan, C |
|
dc.contributor.author |
Tuzcu, M |
|
dc.contributor.author |
Gencoglu, H |
|
dc.contributor.author |
Sahin, N |
|
dc.contributor.author |
Ozercan, IH |
|
dc.contributor.author |
Ali, S |
|
dc.contributor.author |
Yilmaz, I |
|
dc.contributor.author |
Juturu, V |
|
dc.date.accessioned |
2022-09-20T11:47:14Z |
|
dc.date.available |
2022-09-20T11:47:14Z |
|
dc.date.issued |
2019 |
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dc.identifier.uri |
http://hdl.handle.net/11616/61404 |
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dc.description.abstract |
Purpose: Zeaxanthin protects the macula from ocular damage due to light or radiation by scavenging harmful reactive oxygen species. In the present study, zeaxanthin product (OmniXan (R); OMX), derived from paprika pods (Capsicum annum; Family-Solanaceae), was tested for its efficacy in the rat retina against photooxidation. Methods: Forty-two male 8-week-old Wistar rats exposed to 12L/12D, 16L/8D and 24L/0D hours of intense light conditions were orally administrated either 0 or 100 mg/kg BW of zeaxanthin concentration. Retinal morphology was analyzed by histopathology, and target gene expressions were detected with real-time polymerase chain reaction methods. Results: OMX treatment significantly increased the serum zeaxanthin concentration (p < 0.001) and ameliorated oxidative damage by increasing the antioxidant enzyme activities in the retina induced by light (p < 0.001). OMX administration significantly upregulated the expression of genes, including Rhodopsin (Rho), Rod arrestin (SAG), G alpha Transducin 1 (GNAT-1), neural cell adhesion molecule (NCAM), growth-associated protein 43 (GAP43), nuclear factor-(erythroid-derived 2)-like 2 (Nrf2) and heme oxygenase (HO-1) and decreased the expression of nuclear factor-kappa B (NF- kappa B) and GFAP by OMX treatment rats. The histologic findings confirmed the antioxidant and gene expression data. Conclusions: This study suggests that OMX is a potent substance that can be used to protect photoreceptor cell degeneration in the retina exposed to intense light. |
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dc.description.abstract |
C1 [Sahin, Kazim; Orhan, Cemal; Sahin, Nurhan] Firat Univ, Fac Vet Sci, Dept Anim Nutr, Elazig, Turkey. |
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dc.description.abstract |
[Sahin, Kazim; Akdemir, Fatih] Inonu Univ, Fac Fisheries, Dept Nutr, Malatya, Turkey. |
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dc.description.abstract |
[Tuzcu, Mehmet; Gencoglu, Hasan] Firat Univ, Fac Sci, Div Biol, Elazig, Turkey. |
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dc.description.abstract |
[Ozercan, Ibrahim H.] Firat Univ, Fac Med, Dept Pathol, Elazig, Turkey. |
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dc.description.abstract |
[Ali, Shakir] Jamia Hamdard, Fac Sci, Dept Biochem, New Delhi, India. |
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dc.description.abstract |
[Yilmaz, Ismet] Inonu Univ, Fac Pharm, Dept Pharmacol, Malatya, Turkey. |
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dc.description.abstract |
[Juturu, Vijaya] OmniAct Hlth Technol Inc, Res & Dev, Morristown, NJ USA. |
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dc.source |
CUTANEOUS AND OCULAR TOXICOLOGY |
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dc.title |
(3R, 3'R)-zeaxanthin protects the retina from photo-oxidative damage via |
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dc.title |
modulating the inflammation and visual health molecular markers |
|