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Treadmill Exercise Attenuates Retinal Oxidative Stress in Naturally-Aged Mice: An Immunohistochemical Study
In the retina, a number of degenerative diseases, including glaucoma, diabetic retinopathy, and age-related macular degeneration, may occur as a result of aging. Oxidative damage is believed to contribute to the pathogenesis of aging as well as to age-related retinal disease. Although physiological...
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Published in: | International journal of molecular sciences 2015-09, Vol.16 (9), p.21008-21020 |
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description | In the retina, a number of degenerative diseases, including glaucoma, diabetic retinopathy, and age-related macular degeneration, may occur as a result of aging. Oxidative damage is believed to contribute to the pathogenesis of aging as well as to age-related retinal disease. Although physiological exercise has been shown to reduce oxidative stress in rats and mice, it is not known whether it has a similar effect in retinal tissues. The aim of this study was to evaluate retinal oxidative stress in naturally-aged mice. In addition, we evaluated the effects of aerobic training on retinal oxidative stress by immunohistochemically evaluating oxidative stress markers. A group of twelve-week-old male mice were not exercised (young control). Two groups of twenty-two-month-old male mice were created: an old control group and a treadmill exercise group. The old control group mice were not exercised. The treadmill exercise group mice ran on a treadmill (5 to 12 m/min, 30 to 60 min/day, 3 days/week for 12 weeks). The retinal thickness and number of cells in the ganglion cell layer of the naturally-aged mice were reduced compared to those in the young control mice. However, treadmill exercise reversed these morphological changes in the retinas. We evaluated retinal expression of carboxymethyllysine (CML), 8-hydroxy-2'-deoxyguanosine (8-OHdG) and nitrotyrosine. The retinas from the aged mice showed increased CML, 8-OHdG, and nitrotyrosine immunostaining intensities compared to young control mice. The exercise group exhibited significantly lower CML levels and nitro-oxidative stress than the old control group. These results suggest that regular exercise can reduce retinal oxidative stress and that physiological exercise may be distinctly advantageous in reducing retinal oxidative stress. |
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Oxidative damage is believed to contribute to the pathogenesis of aging as well as to age-related retinal disease. Although physiological exercise has been shown to reduce oxidative stress in rats and mice, it is not known whether it has a similar effect in retinal tissues. The aim of this study was to evaluate retinal oxidative stress in naturally-aged mice. In addition, we evaluated the effects of aerobic training on retinal oxidative stress by immunohistochemically evaluating oxidative stress markers. A group of twelve-week-old male mice were not exercised (young control). Two groups of twenty-two-month-old male mice were created: an old control group and a treadmill exercise group. The old control group mice were not exercised. The treadmill exercise group mice ran on a treadmill (5 to 12 m/min, 30 to 60 min/day, 3 days/week for 12 weeks). The retinal thickness and number of cells in the ganglion cell layer of the naturally-aged mice were reduced compared to those in the young control mice. However, treadmill exercise reversed these morphological changes in the retinas. We evaluated retinal expression of carboxymethyllysine (CML), 8-hydroxy-2'-deoxyguanosine (8-OHdG) and nitrotyrosine. The retinas from the aged mice showed increased CML, 8-OHdG, and nitrotyrosine immunostaining intensities compared to young control mice. The exercise group exhibited significantly lower CML levels and nitro-oxidative stress than the old control group. These results suggest that regular exercise can reduce retinal oxidative stress and that physiological exercise may be distinctly advantageous in reducing retinal oxidative stress.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms160921008</identifier><identifier>PMID: 26404251</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>8-Hydroxy-2'-Deoxyguanosine ; aging ; Aging - metabolism ; Aging - physiology ; Animals ; Deoxyguanosine - analogs & derivatives ; Deoxyguanosine - metabolism ; exercise ; Eye diseases ; Lysine - analogs & derivatives ; Lysine - metabolism ; Male ; Mice ; Oxidative Stress ; Physical Conditioning, Animal - methods ; Physical Conditioning, Animal - physiology ; Retina ; Retina - cytology ; Retina - metabolism ; Rodents ; Studies ; treadmill ; Tyrosine - analogs & derivatives ; Tyrosine - metabolism</subject><ispartof>International journal of molecular sciences, 2015-09, Vol.16 (9), p.21008-21020</ispartof><rights>Copyright MDPI AG 2015</rights><rights>2015 by the authors; licensee MDPI, Basel, Switzerland. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c580t-119b5d0db1ac54d877ab9ab8cd1fbf91cd7aa2870188365513c90939932aade33</citedby><cites>FETCH-LOGICAL-c580t-119b5d0db1ac54d877ab9ab8cd1fbf91cd7aa2870188365513c90939932aade33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1793003769/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1793003769?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26404251$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Chan-Sik</creatorcontrib><creatorcontrib>Park, Sok</creatorcontrib><creatorcontrib>Chun, Yoonseok</creatorcontrib><creatorcontrib>Song, Wook</creatorcontrib><creatorcontrib>Kim, Hee-Jae</creatorcontrib><creatorcontrib>Kim, Junghyun</creatorcontrib><title>Treadmill Exercise Attenuates Retinal Oxidative Stress in Naturally-Aged Mice: An Immunohistochemical Study</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>In the retina, a number of degenerative diseases, including glaucoma, diabetic retinopathy, and age-related macular degeneration, may occur as a result of aging. Oxidative damage is believed to contribute to the pathogenesis of aging as well as to age-related retinal disease. Although physiological exercise has been shown to reduce oxidative stress in rats and mice, it is not known whether it has a similar effect in retinal tissues. The aim of this study was to evaluate retinal oxidative stress in naturally-aged mice. In addition, we evaluated the effects of aerobic training on retinal oxidative stress by immunohistochemically evaluating oxidative stress markers. A group of twelve-week-old male mice were not exercised (young control). Two groups of twenty-two-month-old male mice were created: an old control group and a treadmill exercise group. The old control group mice were not exercised. The treadmill exercise group mice ran on a treadmill (5 to 12 m/min, 30 to 60 min/day, 3 days/week for 12 weeks). The retinal thickness and number of cells in the ganglion cell layer of the naturally-aged mice were reduced compared to those in the young control mice. However, treadmill exercise reversed these morphological changes in the retinas. We evaluated retinal expression of carboxymethyllysine (CML), 8-hydroxy-2'-deoxyguanosine (8-OHdG) and nitrotyrosine. The retinas from the aged mice showed increased CML, 8-OHdG, and nitrotyrosine immunostaining intensities compared to young control mice. The exercise group exhibited significantly lower CML levels and nitro-oxidative stress than the old control group. These results suggest that regular exercise can reduce retinal oxidative stress and that physiological exercise may be distinctly advantageous in reducing retinal oxidative stress.</description><subject>8-Hydroxy-2'-Deoxyguanosine</subject><subject>aging</subject><subject>Aging - metabolism</subject><subject>Aging - physiology</subject><subject>Animals</subject><subject>Deoxyguanosine - analogs & derivatives</subject><subject>Deoxyguanosine - metabolism</subject><subject>exercise</subject><subject>Eye diseases</subject><subject>Lysine - analogs & derivatives</subject><subject>Lysine - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Oxidative Stress</subject><subject>Physical Conditioning, Animal - methods</subject><subject>Physical Conditioning, Animal - physiology</subject><subject>Retina</subject><subject>Retina - cytology</subject><subject>Retina - metabolism</subject><subject>Rodents</subject><subject>Studies</subject><subject>treadmill</subject><subject>Tyrosine - analogs & derivatives</subject><subject>Tyrosine - metabolism</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkk1v1DAQhiMEomXhyBVF4sIlMP6KbQ5Iq6rASoVKtJwtx57seslHaztV99-TsqXqcuJky_P40YzmLYrXBN4zpuFD2PaJ1KApAVBPimPCKa0Aavn00f2oeJHSFoAyKvTz4ojWHDgV5Lj4dRnR-j50XXl6i9GFhOUyZxwmmzGVPzCHwXbl-W3wNocbLC9yxJTKMJTfbZ6i7bpdtVyjL78Fhx_L5VCu-n4axk1IeXQb7IOb_1_kye9eFs9a2yV8dX8uip-fTy9PvlZn519WJ8uzygkFuSJEN8KDb4h1gnslpW20bZTzpG1aTZyX1lIlgSjFaiEIcxo005pRaz0ytihWe68f7dZcxdDbuDOjDebPwxjXxsYcXIemFpIjkaQVnHONytba1r7lmgIXrYDZ9WnvupqaHr3DIc8zH0gPK0PYmPV4Y3hNGGVqFry7F8TxesKUTR-Sw66zA45TMkQxyRin8B-oJAqkFrN5Ubz9B92OU5w3dUdpBsBkrWeq2lMujilFbB_6JmDu0mMO0jPzbx4P-0D_jQv7DWjpwEA</recordid><startdate>20150902</startdate><enddate>20150902</enddate><creator>Kim, Chan-Sik</creator><creator>Park, Sok</creator><creator>Chun, Yoonseok</creator><creator>Song, Wook</creator><creator>Kim, Hee-Jae</creator><creator>Kim, Junghyun</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7TK</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150902</creationdate><title>Treadmill Exercise Attenuates Retinal Oxidative Stress in Naturally-Aged Mice: An Immunohistochemical Study</title><author>Kim, Chan-Sik ; Park, Sok ; Chun, Yoonseok ; Song, Wook ; Kim, Hee-Jae ; Kim, Junghyun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c580t-119b5d0db1ac54d877ab9ab8cd1fbf91cd7aa2870188365513c90939932aade33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>8-Hydroxy-2'-Deoxyguanosine</topic><topic>aging</topic><topic>Aging - metabolism</topic><topic>Aging - physiology</topic><topic>Animals</topic><topic>Deoxyguanosine - analogs & derivatives</topic><topic>Deoxyguanosine - metabolism</topic><topic>exercise</topic><topic>Eye diseases</topic><topic>Lysine - analogs & derivatives</topic><topic>Lysine - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Oxidative Stress</topic><topic>Physical Conditioning, Animal - methods</topic><topic>Physical Conditioning, Animal - physiology</topic><topic>Retina</topic><topic>Retina - cytology</topic><topic>Retina - metabolism</topic><topic>Rodents</topic><topic>Studies</topic><topic>treadmill</topic><topic>Tyrosine - analogs & derivatives</topic><topic>Tyrosine - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Chan-Sik</creatorcontrib><creatorcontrib>Park, Sok</creatorcontrib><creatorcontrib>Chun, Yoonseok</creatorcontrib><creatorcontrib>Song, Wook</creatorcontrib><creatorcontrib>Kim, Hee-Jae</creatorcontrib><creatorcontrib>Kim, Junghyun</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Chan-Sik</au><au>Park, Sok</au><au>Chun, Yoonseok</au><au>Song, Wook</au><au>Kim, Hee-Jae</au><au>Kim, Junghyun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treadmill Exercise Attenuates Retinal Oxidative Stress in Naturally-Aged Mice: An Immunohistochemical Study</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2015-09-02</date><risdate>2015</risdate><volume>16</volume><issue>9</issue><spage>21008</spage><epage>21020</epage><pages>21008-21020</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>In the retina, a number of degenerative diseases, including glaucoma, diabetic retinopathy, and age-related macular degeneration, may occur as a result of aging. Oxidative damage is believed to contribute to the pathogenesis of aging as well as to age-related retinal disease. Although physiological exercise has been shown to reduce oxidative stress in rats and mice, it is not known whether it has a similar effect in retinal tissues. The aim of this study was to evaluate retinal oxidative stress in naturally-aged mice. In addition, we evaluated the effects of aerobic training on retinal oxidative stress by immunohistochemically evaluating oxidative stress markers. A group of twelve-week-old male mice were not exercised (young control). Two groups of twenty-two-month-old male mice were created: an old control group and a treadmill exercise group. The old control group mice were not exercised. The treadmill exercise group mice ran on a treadmill (5 to 12 m/min, 30 to 60 min/day, 3 days/week for 12 weeks). The retinal thickness and number of cells in the ganglion cell layer of the naturally-aged mice were reduced compared to those in the young control mice. However, treadmill exercise reversed these morphological changes in the retinas. We evaluated retinal expression of carboxymethyllysine (CML), 8-hydroxy-2'-deoxyguanosine (8-OHdG) and nitrotyrosine. The retinas from the aged mice showed increased CML, 8-OHdG, and nitrotyrosine immunostaining intensities compared to young control mice. The exercise group exhibited significantly lower CML levels and nitro-oxidative stress than the old control group. These results suggest that regular exercise can reduce retinal oxidative stress and that physiological exercise may be distinctly advantageous in reducing retinal oxidative stress.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>26404251</pmid><doi>10.3390/ijms160921008</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 8-Hydroxy-2'-Deoxyguanosine aging Aging - metabolism Aging - physiology Animals Deoxyguanosine - analogs & derivatives Deoxyguanosine - metabolism exercise Eye diseases Lysine - analogs & derivatives Lysine - metabolism Male Mice Oxidative Stress Physical Conditioning, Animal - methods Physical Conditioning, Animal - physiology Retina Retina - cytology Retina - metabolism Rodents Studies treadmill Tyrosine - analogs & derivatives Tyrosine - metabolism |
title | Treadmill Exercise Attenuates Retinal Oxidative Stress in Naturally-Aged Mice: An Immunohistochemical Study |
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