Protection of rabbit retina from ischemic injury by superoxide dismutase and catalase
To provide evidence that free radical damage is a component of postischemic retinal injury; to determine whether antioxidant enzymes, superoxide dismutase (SOD) and catalase, can protect the retina from ischemic injury. Total retinal ischemia for 60 or 75 min was produced in Dutch rabbits by raising...
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Veröffentlicht in: | Investigative ophthalmology & visual science 1993-05, Vol.34 (6), p.2018-2022 |
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creator | Nayak, MS Kita, M Marmor, MF |
description | To provide evidence that free radical damage is a component of postischemic retinal injury; to determine whether antioxidant enzymes, superoxide dismutase (SOD) and catalase, can protect the retina from ischemic injury.
Total retinal ischemia for 60 or 75 min was produced in Dutch rabbits by raising intraocular pressure. Retinal recovery was monitored with the electroretinogram. Enzymes were administered as an intravenous bolus dose 2-3 min before restoration of circulation.
In eyes subjected to 60 min ischemia, the amplitude of the a-wave 4 hours after reperfusion averaged 114.9% of baseline value in control rabbits and 126.5% in SOD-treated animals. The b-wave amplitude at this time was 79.3% and 106.8% in control rabbits and SOD-treated rabbits, respectively. After an ischemic insult of 75 min, at 4 hours the a-wave amplitude was 89.2% of baseline in control eyes, 108.8% in SOD-treated eyes, 159.6% in eyes that received a combination of SOD and catalase, and 149.8% in catalase-treated eyes. The amplitude of the b-wave was reduced to 47.8% in control eyes and 44.8% in SOD-treated eyes, but recovered to 92.3% in rabbits that received the combination therapy and 98.8% in animals that received catalase alone.
These findings suggest that free radical generation is involved in ischemic tissue damage. The fact that antioxidant enzymes can be protective has implications for the treatment of acute ischemic diseases of the retina. |
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Total retinal ischemia for 60 or 75 min was produced in Dutch rabbits by raising intraocular pressure. Retinal recovery was monitored with the electroretinogram. Enzymes were administered as an intravenous bolus dose 2-3 min before restoration of circulation.
In eyes subjected to 60 min ischemia, the amplitude of the a-wave 4 hours after reperfusion averaged 114.9% of baseline value in control rabbits and 126.5% in SOD-treated animals. The b-wave amplitude at this time was 79.3% and 106.8% in control rabbits and SOD-treated rabbits, respectively. After an ischemic insult of 75 min, at 4 hours the a-wave amplitude was 89.2% of baseline in control eyes, 108.8% in SOD-treated eyes, 159.6% in eyes that received a combination of SOD and catalase, and 149.8% in catalase-treated eyes. The amplitude of the b-wave was reduced to 47.8% in control eyes and 44.8% in SOD-treated eyes, but recovered to 92.3% in rabbits that received the combination therapy and 98.8% in animals that received catalase alone.
These findings suggest that free radical generation is involved in ischemic tissue damage. The fact that antioxidant enzymes can be protective has implications for the treatment of acute ischemic diseases of the retina.</description><identifier>ISSN: 0146-0404</identifier><identifier>EISSN: 1552-5783</identifier><identifier>PMID: 8491552</identifier><identifier>CODEN: IOVSDA</identifier><language>eng</language><publisher>Rockville, MD: ARVO</publisher><subject>Animals ; Biological and medical sciences ; Catalase - therapeutic use ; Disease Models, Animal ; Electroretinography ; Eye ; Free Radicals ; Injections, Intravenous ; Ischemia - physiopathology ; Ischemia - prevention & control ; Medical sciences ; Pharmacology. Drug treatments ; Photoreceptor Cells - physiology ; Rabbits ; Retinal Vessels - drug effects ; Superoxide Dismutase - therapeutic use</subject><ispartof>Investigative ophthalmology & visual science, 1993-05, Vol.34 (6), p.2018-2022</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4781789$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8491552$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nayak, MS</creatorcontrib><creatorcontrib>Kita, M</creatorcontrib><creatorcontrib>Marmor, MF</creatorcontrib><title>Protection of rabbit retina from ischemic injury by superoxide dismutase and catalase</title><title>Investigative ophthalmology & visual science</title><addtitle>Invest Ophthalmol Vis Sci</addtitle><description>To provide evidence that free radical damage is a component of postischemic retinal injury; to determine whether antioxidant enzymes, superoxide dismutase (SOD) and catalase, can protect the retina from ischemic injury.
Total retinal ischemia for 60 or 75 min was produced in Dutch rabbits by raising intraocular pressure. Retinal recovery was monitored with the electroretinogram. Enzymes were administered as an intravenous bolus dose 2-3 min before restoration of circulation.
In eyes subjected to 60 min ischemia, the amplitude of the a-wave 4 hours after reperfusion averaged 114.9% of baseline value in control rabbits and 126.5% in SOD-treated animals. The b-wave amplitude at this time was 79.3% and 106.8% in control rabbits and SOD-treated rabbits, respectively. After an ischemic insult of 75 min, at 4 hours the a-wave amplitude was 89.2% of baseline in control eyes, 108.8% in SOD-treated eyes, 159.6% in eyes that received a combination of SOD and catalase, and 149.8% in catalase-treated eyes. The amplitude of the b-wave was reduced to 47.8% in control eyes and 44.8% in SOD-treated eyes, but recovered to 92.3% in rabbits that received the combination therapy and 98.8% in animals that received catalase alone.
These findings suggest that free radical generation is involved in ischemic tissue damage. The fact that antioxidant enzymes can be protective has implications for the treatment of acute ischemic diseases of the retina.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Catalase - therapeutic use</subject><subject>Disease Models, Animal</subject><subject>Electroretinography</subject><subject>Eye</subject><subject>Free Radicals</subject><subject>Injections, Intravenous</subject><subject>Ischemia - physiopathology</subject><subject>Ischemia - prevention & control</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Photoreceptor Cells - physiology</subject><subject>Rabbits</subject><subject>Retinal Vessels - drug effects</subject><subject>Superoxide Dismutase - therapeutic use</subject><issn>0146-0404</issn><issn>1552-5783</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtLxDAUhYso4zj6E4QsxF0hzyZdyuALBF2M65AmtzZDH2OSUuffW7Ho6t7L-TjncE-yNRGC5kIqdpqtMeFFjjnm59lFjHuMKSEUr7KV4uUPt87e38KQwCY_9GioUTBV5RMKkHxvUB2GDvloG-i8Rb7fj-GIqiOK4wHC8OUdIOdjNyYTAZneIWuSaefjMjurTRvhapmbbPdwv9s-5S-vj8_bu5e8oUWRciFKQgswoFjpyrooMCjHMbE15kpAyeetJlRQZ0snjJFUcWCK4ppjWQLbZLe_tocwfI4Qk-7mttC2podhjFoKyahkfAavF3CsOnD6EHxnwlEvb5j1m0U30Zq2Dqa3Pv5hXCoiVfmf1_iPZvIBdOxM286mRE_TxLguNMVEsW-qpnRO</recordid><startdate>19930501</startdate><enddate>19930501</enddate><creator>Nayak, MS</creator><creator>Kita, M</creator><creator>Marmor, MF</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>7X8</scope></search><sort><creationdate>19930501</creationdate><title>Protection of rabbit retina from ischemic injury by superoxide dismutase and catalase</title><author>Nayak, MS ; Kita, M ; Marmor, MF</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h266t-559126eae839d9f660e8d401cf0485e941cff1252dc9d5aa7284e3820f4079e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Catalase - therapeutic use</topic><topic>Disease Models, Animal</topic><topic>Electroretinography</topic><topic>Eye</topic><topic>Free Radicals</topic><topic>Injections, Intravenous</topic><topic>Ischemia - physiopathology</topic><topic>Ischemia - prevention & control</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Photoreceptor Cells - physiology</topic><topic>Rabbits</topic><topic>Retinal Vessels - drug effects</topic><topic>Superoxide Dismutase - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nayak, MS</creatorcontrib><creatorcontrib>Kita, M</creatorcontrib><creatorcontrib>Marmor, MF</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>MEDLINE - Academic</collection><jtitle>Investigative ophthalmology & visual science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nayak, MS</au><au>Kita, M</au><au>Marmor, MF</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protection of rabbit retina from ischemic injury by superoxide dismutase and catalase</atitle><jtitle>Investigative ophthalmology & visual science</jtitle><addtitle>Invest Ophthalmol Vis Sci</addtitle><date>1993-05-01</date><risdate>1993</risdate><volume>34</volume><issue>6</issue><spage>2018</spage><epage>2022</epage><pages>2018-2022</pages><issn>0146-0404</issn><eissn>1552-5783</eissn><coden>IOVSDA</coden><abstract>To provide evidence that free radical damage is a component of postischemic retinal injury; to determine whether antioxidant enzymes, superoxide dismutase (SOD) and catalase, can protect the retina from ischemic injury.
Total retinal ischemia for 60 or 75 min was produced in Dutch rabbits by raising intraocular pressure. Retinal recovery was monitored with the electroretinogram. Enzymes were administered as an intravenous bolus dose 2-3 min before restoration of circulation.
In eyes subjected to 60 min ischemia, the amplitude of the a-wave 4 hours after reperfusion averaged 114.9% of baseline value in control rabbits and 126.5% in SOD-treated animals. The b-wave amplitude at this time was 79.3% and 106.8% in control rabbits and SOD-treated rabbits, respectively. After an ischemic insult of 75 min, at 4 hours the a-wave amplitude was 89.2% of baseline in control eyes, 108.8% in SOD-treated eyes, 159.6% in eyes that received a combination of SOD and catalase, and 149.8% in catalase-treated eyes. The amplitude of the b-wave was reduced to 47.8% in control eyes and 44.8% in SOD-treated eyes, but recovered to 92.3% in rabbits that received the combination therapy and 98.8% in animals that received catalase alone.
These findings suggest that free radical generation is involved in ischemic tissue damage. The fact that antioxidant enzymes can be protective has implications for the treatment of acute ischemic diseases of the retina.</abstract><cop>Rockville, MD</cop><pub>ARVO</pub><pmid>8491552</pmid><tpages>5</tpages></addata></record> |
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source | MEDLINE; EZB-FREE-00999 freely available EZB journals |
subjects | Animals Biological and medical sciences Catalase - therapeutic use Disease Models, Animal Electroretinography Eye Free Radicals Injections, Intravenous Ischemia - physiopathology Ischemia - prevention & control Medical sciences Pharmacology. Drug treatments Photoreceptor Cells - physiology Rabbits Retinal Vessels - drug effects Superoxide Dismutase - therapeutic use |
title | Protection of rabbit retina from ischemic injury by superoxide dismutase and catalase |
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