Microalga Chlorella sp. biomass containing high lutein prevents light-induced photooxidation and retinal degeneration in mice

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dc.contributor.authorH Y Yu-
dc.contributor.authorDae Hyun Cho-
dc.contributor.authorD Seo-
dc.contributor.authorC Yoo-
dc.contributor.authorS B Park-
dc.contributor.authorW K Jung-
dc.contributor.authorJ E Jung-
dc.contributor.authorHee-Sik Kim-
dc.contributor.authorJ Kim-
dc.date.accessioned2024-08-06T16:33:04Z-
dc.date.available2024-08-06T16:33:04Z-
dc.date.issued2024-
dc.identifier.issn2211-9264-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/35559-
dc.description.abstractAge-related macular degeneration (AMD) is commonly associated with retinal degeneration. Carotenoids, particularly lutein, can protect against AMD. Chlorella sp. has been widely used as a dietary supplement and contained high levels of lutein. Chlorella sp. biomass ethanol extract containing high lutein concentrations (CEE) was tested for its retinoprotective effects in retinal pigment epithelial (RPE) cells and light exposure-induced retinal degeneration in mice. The inhibitory activity of CEE on photooxidation of Bis-retinoid N-retinyl-N-retinylidene ethanolamine (A2E) was assessed in ARPE-19 cells. Retinal degeneration was induced by the exposure to 5000 lx of white LED light for 3 h. For one week, CEE (10, 25 and 50 mg/kg) and lutein (25 mg/kg) were administered orally. A retinal electroretinography (ERG) and a histological examination were conducted. Furthermore, oxidative DNA damage and apoptosis were quantified in the retina. CEE and lutein inhibited the A2E photooxidation and oxidized A2E-induced RPE injury. The results of an in vivo experiment also demonstrate that CEE and lutein have powerful anti-oxidative and anti-apoptotic effects on mice with light-induced retinal degeneration. There were fewer histological changes in the ONL layer in mice that were treated with CEE and lutein. CEE and lutein have both a- and b-wave amplitude increments in ERG analysis. The TUNEL-positive cells and 8-OHdG expression in the retinas were reduced by CEE and lutein. CEE may prevent retinal photoreceptors from light-induced structural and functional damage. The active ingredient, lutein, is responsible for this retinoprotective activity. CEE can provide the additional benefit in patients with retinal degenerative diseases.-
dc.publisherElsevier-
dc.titleMicroalga Chlorella sp. biomass containing high lutein prevents light-induced photooxidation and retinal degeneration in mice-
dc.title.alternativeMicroalga Chlorella sp. biomass containing high lutein prevents light-induced photooxidation and retinal degeneration in mice-
dc.typeArticle-
dc.citation.titleAlgal Research-Biomass Biofuels and Bioproducts-
dc.citation.number0-
dc.citation.endPage103620-
dc.citation.startPage103620-
dc.citation.volume82-
dc.contributor.affiliatedAuthorDae Hyun Cho-
dc.contributor.affiliatedAuthorHee-Sik Kim-
dc.contributor.alternativeName유화영-
dc.contributor.alternativeName조대현-
dc.contributor.alternativeName서대방-
dc.contributor.alternativeName유찬-
dc.contributor.alternativeName박수빈-
dc.contributor.alternativeName정우권-
dc.contributor.alternativeName정재은-
dc.contributor.alternativeName김희식-
dc.contributor.alternativeName김정현-
dc.identifier.bibliographicCitationAlgal Research-Biomass Biofuels and Bioproducts, vol. 82, pp. 103620-103620-
dc.identifier.doi10.1016/j.algal.2024.103620-
dc.subject.keywordAge-related macular degeneration-
dc.subject.keywordChlorella-
dc.subject.keywordLutein-
dc.subject.keywordOxidative stress-
dc.subject.keywordRetinal degeneration-
dc.subject.localAge-related macular degeneration-
dc.subject.localAge-related Macular Degeneration-
dc.subject.localage-related macular degeneration-
dc.subject.localChlorella-
dc.subject.localchlorella-
dc.subject.locallutein-
dc.subject.localLutein-
dc.subject.localOXIDATIVE STRESS-
dc.subject.localOxidative Stress-
dc.subject.localOxidative stre-
dc.subject.localOxidative stress-
dc.subject.localoxidative stress-
dc.description.journalClassY-
Appears in Collections:
Synthetic Biology and Bioengineering Research Institute > Cell Factory Research Center > 1. Journal Articles
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