Saffron Supplement Maintains Morphology and Function after Exposure to Damaging Light in Mammalian Retina

To test whether the saffron extract (Crocus sativus L.) given as a dietary supplement counteracts the effects of continuous light exposure in the albino rat retina. Three experimental groups of Sprague-Dawley rats were used. Experimental animals were prefed either saffron or beta-carotene (1 mg extr...

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Veröffentlicht in:Investigative ophthalmology & visual science 2008-03, Vol.49 (3), p.1254-1261
Hauptverfasser: Maccarone, Rita, Di Marco, Stefano, Bisti, Silvia
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Di Marco, Stefano
Bisti, Silvia
description To test whether the saffron extract (Crocus sativus L.) given as a dietary supplement counteracts the effects of continuous light exposure in the albino rat retina. Three experimental groups of Sprague-Dawley rats were used. Experimental animals were prefed either saffron or beta-carotene (1 mg extract/kg/d) before they were exposed to bright continuous light (BCL) for 24 hours. Flash electroretinograms (fERGs) were recorded in control and treated rats the day before and 1 week after light exposure. At the end of the second recording session, the animals were killed and the retinas were quickly removed, fixed, cryosectioned, and labeled so that the thickness of the outer nuclear layer (ONL) could be analyzed. Changes in protein level and cellular localization of fibroblast growth factor (FGF)2 were determined by Western blot analysis and retinal immunohistochemistry, respectively. In a second series of experiments, rats were killed at the end of light exposure, and the amount of apoptotic figures in the ONL was assessed by terminal transferase-mediated deoxyuridine triphosphate (d-UTP)-biotin nick-end labeling (TUNEL). BCL induced DNA fragmentation, characteristic of dying cells, almost exclusively in the photoreceptor layer. The rate of photoreceptor death induced by BCL is expressed as the frequency of TUNEL-positive profiles per millimeter. The photoreceptor layer was largely preserved in saffron-treated animals because it was the fERG response. In addition, the rate of photoreceptor death induced by BCL appeared drastically reduced in treated animals. In beta-carotene prefeeding experiments, morphologic analysis showed preservation of the ONL similar to that obtained with saffron prefeeding, whereas the fERG response was unrecordable. Western blot analysis showed that exposure to light induced a strong upregulation of FGF2 in control and beta-carotene-treated rats, but s no change was noted in saffron-treated rats. These results show that saffron may protect photoreceptors from retinal stress, maintaining both morphology and function and probably acting as a regulator of programmed cell death.
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BCL induced DNA fragmentation, characteristic of dying cells, almost exclusively in the photoreceptor layer. The rate of photoreceptor death induced by BCL is expressed as the frequency of TUNEL-positive profiles per millimeter. The photoreceptor layer was largely preserved in saffron-treated animals because it was the fERG response. In addition, the rate of photoreceptor death induced by BCL appeared drastically reduced in treated animals. In beta-carotene prefeeding experiments, morphologic analysis showed preservation of the ONL similar to that obtained with saffron prefeeding, whereas the fERG response was unrecordable. Western blot analysis showed that exposure to light induced a strong upregulation of FGF2 in control and beta-carotene-treated rats, but s no change was noted in saffron-treated rats. 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BCL induced DNA fragmentation, characteristic of dying cells, almost exclusively in the photoreceptor layer. The rate of photoreceptor death induced by BCL is expressed as the frequency of TUNEL-positive profiles per millimeter. The photoreceptor layer was largely preserved in saffron-treated animals because it was the fERG response. In addition, the rate of photoreceptor death induced by BCL appeared drastically reduced in treated animals. In beta-carotene prefeeding experiments, morphologic analysis showed preservation of the ONL similar to that obtained with saffron prefeeding, whereas the fERG response was unrecordable. Western blot analysis showed that exposure to light induced a strong upregulation of FGF2 in control and beta-carotene-treated rats, but s no change was noted in saffron-treated rats. These results show that saffron may protect photoreceptors from retinal stress, maintaining both morphology and function and probably acting as a regulator of programmed cell death.</description><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>beta Carotene - administration &amp; dosage</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Crocus</subject><subject>Dark Adaptation</subject><subject>Electroretinography</subject><subject>Eye and associated structures. Visual pathways and centers. Vision</subject><subject>Fibroblast Growth Factor 2 - metabolism</subject><subject>Flowers</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>In Situ Nick-End Labeling</subject><subject>Light - adverse effects</subject><subject>Medical sciences</subject><subject>Ophthalmology</subject><subject>Oxidative Stress</subject><subject>Photic Stimulation</subject><subject>Plant Extracts - administration &amp; dosage</subject><subject>Radiation Injuries, Experimental - metabolism</subject><subject>Radiation Injuries, Experimental - pathology</subject><subject>Radiation Injuries, Experimental - prevention &amp; control</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Retina - physiology</subject><subject>Retina - radiation effects</subject><subject>Retinal Degeneration - metabolism</subject><subject>Retinal Degeneration - pathology</subject><subject>Retinal Degeneration - prevention &amp; control</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0146-0404</issn><issn>1552-5783</issn><issn>1552-5783</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1rGzEQhkVISVy3t56LLsmpm2okrVY-hny0BYdC057FrFayFXa1i7Sum39fGZv2MLwwPLzMPIR8AHYDoJrPYfydb1hTMSn0GVlAXfOqbrQ4JwsGUpU9k5fkbc4vjHEAzi7IJWjBVVOrBQnP6H0aI33eTVPvBhdn-oQhzmUyfRrTtB37cfNKMXb0cRftHAqMfnaJPvyZxrxLjs4jvccBNyFu6DpstjMNsbQMA_YBI_3h5hDxHXnjsc_u_SmX5Nfjw8-7r9X6-5dvd7frykpQcwVOryw4pVprNROIjReyliiUV9DpWijdcuQtXymw4EW94rbRXHeStV52rViST8dem8ack_NmSmHA9GqAmYMxczBmWGMOxgr-8YhPu3Zw3X_4pKgAVycAs8XeJ4w25H8cZ6A4L5cuyfWR2xYD-5CcyeX_vtSC2e_3cmWEAV5L8RfTZIKL</recordid><startdate>20080301</startdate><enddate>20080301</enddate><creator>Maccarone, Rita</creator><creator>Di Marco, Stefano</creator><creator>Bisti, Silvia</creator><general>ARVO</general><general>Association for Research in Vision and Ophtalmology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20080301</creationdate><title>Saffron Supplement Maintains Morphology and Function after Exposure to Damaging Light in Mammalian Retina</title><author>Maccarone, Rita ; Di Marco, Stefano ; Bisti, Silvia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-1e89c1e66bcc803aa7f3454a36f61d85368b2a2b2961c1f3592c7828d40bf4db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>beta Carotene - administration &amp; dosage</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Crocus</topic><topic>Dark Adaptation</topic><topic>Electroretinography</topic><topic>Eye and associated structures. Visual pathways and centers. Vision</topic><topic>Fibroblast Growth Factor 2 - metabolism</topic><topic>Flowers</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>In Situ Nick-End Labeling</topic><topic>Light - adverse effects</topic><topic>Medical sciences</topic><topic>Ophthalmology</topic><topic>Oxidative Stress</topic><topic>Photic Stimulation</topic><topic>Plant Extracts - administration &amp; dosage</topic><topic>Radiation Injuries, Experimental - metabolism</topic><topic>Radiation Injuries, Experimental - pathology</topic><topic>Radiation Injuries, Experimental - prevention &amp; control</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Retina - physiology</topic><topic>Retina - radiation effects</topic><topic>Retinal Degeneration - metabolism</topic><topic>Retinal Degeneration - pathology</topic><topic>Retinal Degeneration - prevention &amp; control</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maccarone, Rita</creatorcontrib><creatorcontrib>Di Marco, Stefano</creatorcontrib><creatorcontrib>Bisti, Silvia</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Investigative ophthalmology &amp; visual science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maccarone, Rita</au><au>Di Marco, Stefano</au><au>Bisti, Silvia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Saffron Supplement Maintains Morphology and Function after Exposure to Damaging Light in Mammalian Retina</atitle><jtitle>Investigative ophthalmology &amp; visual science</jtitle><addtitle>Invest Ophthalmol Vis Sci</addtitle><date>2008-03-01</date><risdate>2008</risdate><volume>49</volume><issue>3</issue><spage>1254</spage><epage>1261</epage><pages>1254-1261</pages><issn>0146-0404</issn><issn>1552-5783</issn><eissn>1552-5783</eissn><coden>IOVSDA</coden><abstract>To test whether the saffron extract (Crocus sativus L.) given as a dietary supplement counteracts the effects of continuous light exposure in the albino rat retina. Three experimental groups of Sprague-Dawley rats were used. Experimental animals were prefed either saffron or beta-carotene (1 mg extract/kg/d) before they were exposed to bright continuous light (BCL) for 24 hours. Flash electroretinograms (fERGs) were recorded in control and treated rats the day before and 1 week after light exposure. At the end of the second recording session, the animals were killed and the retinas were quickly removed, fixed, cryosectioned, and labeled so that the thickness of the outer nuclear layer (ONL) could be analyzed. Changes in protein level and cellular localization of fibroblast growth factor (FGF)2 were determined by Western blot analysis and retinal immunohistochemistry, respectively. In a second series of experiments, rats were killed at the end of light exposure, and the amount of apoptotic figures in the ONL was assessed by terminal transferase-mediated deoxyuridine triphosphate (d-UTP)-biotin nick-end labeling (TUNEL). BCL induced DNA fragmentation, characteristic of dying cells, almost exclusively in the photoreceptor layer. The rate of photoreceptor death induced by BCL is expressed as the frequency of TUNEL-positive profiles per millimeter. The photoreceptor layer was largely preserved in saffron-treated animals because it was the fERG response. In addition, the rate of photoreceptor death induced by BCL appeared drastically reduced in treated animals. In beta-carotene prefeeding experiments, morphologic analysis showed preservation of the ONL similar to that obtained with saffron prefeeding, whereas the fERG response was unrecordable. Western blot analysis showed that exposure to light induced a strong upregulation of FGF2 in control and beta-carotene-treated rats, but s no change was noted in saffron-treated rats. These results show that saffron may protect photoreceptors from retinal stress, maintaining both morphology and function and probably acting as a regulator of programmed cell death.</abstract><cop>Rockville, MD</cop><pub>ARVO</pub><pmid>18326756</pmid><doi>10.1167/iovs.07-0438</doi><tpages>8</tpages></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Animals
Apoptosis - drug effects
beta Carotene - administration & dosage
Biological and medical sciences
Blotting, Western
Crocus
Dark Adaptation
Electroretinography
Eye and associated structures. Visual pathways and centers. Vision
Fibroblast Growth Factor 2 - metabolism
Flowers
Fluorescent Antibody Technique, Indirect
Fundamental and applied biological sciences. Psychology
In Situ Nick-End Labeling
Light - adverse effects
Medical sciences
Ophthalmology
Oxidative Stress
Photic Stimulation
Plant Extracts - administration & dosage
Radiation Injuries, Experimental - metabolism
Radiation Injuries, Experimental - pathology
Radiation Injuries, Experimental - prevention & control
Rats
Rats, Sprague-Dawley
Retina - physiology
Retina - radiation effects
Retinal Degeneration - metabolism
Retinal Degeneration - pathology
Retinal Degeneration - prevention & control
Vertebrates: nervous system and sense organs
title Saffron Supplement Maintains Morphology and Function after Exposure to Damaging Light in Mammalian Retina
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