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Article: Delayed post-ischemic conditioning significantly improves the outcome after retinal ischemia
Title | Delayed post-ischemic conditioning significantly improves the outcome after retinal ischemia | ||||||||||||
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Authors | |||||||||||||
Keywords | Ischemia Post-conditioning Rat Retina | ||||||||||||
Issue Date | 2011 | ||||||||||||
Publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/yexer | ||||||||||||
Citation | Experimental Eye Research, 2011, v. 92 n. 6, p. 521-527 How to Cite? | ||||||||||||
Abstract | In previous studies, it was shown that post-conditioning, a transient period of brief ischemia following prolonged severe ischemia in the retina, could provide significant improvement in post-ischemic recovery, attenuation of cell loss, and decreased apoptosis. These studies showed that post-conditioning effectively prevented damage after retinal ischemia when it was instituted early (within 1 h) in the post-ischemic period. While post-ischemic conditioning holds high promise of clinical translation, patients often present late after the onset of retinal ischemia and therefore immediate application of this anti-ischemic maneuver is generally not feasible. In this study, we examined the hypothesis that application of a post-conditioning stimulus at 24 h or greater following the end of prolonged ischemia would decrease the extent of ischemic injury. Ischemia was induced in rat retina in vivo. Recovery after ischemia followed by 5 min of post-conditioning brief ischemia 24 or 48 h after prolonged ischemia was assessed functionally (electroretinography) and histologically at 7 days after ischemia and post-conditioning or sham post-conditioning. We found that the brief ischemic stimulus applied 24, but not 48 h after prolonged ischemia significantly improved functional recovery and decreased histological damage induced by prolonged ischemia. We conclude that within a defined time window, delayed post-ischemic conditioning ameliorated post-ischemic injury in rats. Compared to earlier studies, the present work demonstrates for the first time the novel ability of a significantly delayed ischemic stimulus to provide robust neuroprotection in the retina following ischemia. © 2011 Elsevier Ltd. | ||||||||||||
Persistent Identifier | http://hdl.handle.net/10722/141083 | ||||||||||||
ISSN | 2023 Impact Factor: 3.0 2023 SCImago Journal Rankings: 1.020 | ||||||||||||
PubMed Central ID | |||||||||||||
ISI Accession Number ID |
Funding Information: Supported by National Institutes of Health (Rockville, MD) grants EY10343 and EY10343-16S1 (American Recovery and Reinvestment Act) to Dr Roth, AG029795-02 for the Medical Student Summer Research Program at the Pritzker School of Medicine, UL1RR024999 to the University of Chicago Institute for Translational Medicine; the Illinois Society for the Prevention of Blindness (Chicago, IL); France and Chicago Collaborating in the Sciences (The Chicago-France Center, Chicago, IL); and the Dean's Research Advisory Committee of the Division of Biological Sciences of the University of Chicago. Jacqueline N. Poston was the recipient of a Medical Student Research Fellowship Award from the American Academy of Neurology, St Paul, MN. There is no conflict of interest or commercial interest for any of the authors. | ||||||||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Dreixler, JC | en_HK |
dc.contributor.author | Poston, JN | en_HK |
dc.contributor.author | Shaikh, AR | en_HK |
dc.contributor.author | Alexander, M | en_HK |
dc.contributor.author | Tupper, KY | en_HK |
dc.contributor.author | Marcet, MM | en_HK |
dc.contributor.author | Bernaudin, M | en_HK |
dc.contributor.author | Roth, S | en_HK |
dc.date.accessioned | 2011-09-23T06:25:10Z | - |
dc.date.available | 2011-09-23T06:25:10Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Experimental Eye Research, 2011, v. 92 n. 6, p. 521-527 | en_HK |
dc.identifier.issn | 0014-4835 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/141083 | - |
dc.description.abstract | In previous studies, it was shown that post-conditioning, a transient period of brief ischemia following prolonged severe ischemia in the retina, could provide significant improvement in post-ischemic recovery, attenuation of cell loss, and decreased apoptosis. These studies showed that post-conditioning effectively prevented damage after retinal ischemia when it was instituted early (within 1 h) in the post-ischemic period. While post-ischemic conditioning holds high promise of clinical translation, patients often present late after the onset of retinal ischemia and therefore immediate application of this anti-ischemic maneuver is generally not feasible. In this study, we examined the hypothesis that application of a post-conditioning stimulus at 24 h or greater following the end of prolonged ischemia would decrease the extent of ischemic injury. Ischemia was induced in rat retina in vivo. Recovery after ischemia followed by 5 min of post-conditioning brief ischemia 24 or 48 h after prolonged ischemia was assessed functionally (electroretinography) and histologically at 7 days after ischemia and post-conditioning or sham post-conditioning. We found that the brief ischemic stimulus applied 24, but not 48 h after prolonged ischemia significantly improved functional recovery and decreased histological damage induced by prolonged ischemia. We conclude that within a defined time window, delayed post-ischemic conditioning ameliorated post-ischemic injury in rats. Compared to earlier studies, the present work demonstrates for the first time the novel ability of a significantly delayed ischemic stimulus to provide robust neuroprotection in the retina following ischemia. © 2011 Elsevier Ltd. | en_HK |
dc.language | eng | en_US |
dc.publisher | Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/yexer | en_HK |
dc.relation.ispartof | Experimental Eye Research | en_HK |
dc.subject | Ischemia | en_HK |
dc.subject | Post-conditioning | en_HK |
dc.subject | Rat | en_HK |
dc.subject | Retina | en_HK |
dc.subject.mesh | Apoptosis - physiology | - |
dc.subject.mesh | Ischemic Postconditioning | - |
dc.subject.mesh | Reperfusion Injury - physiopathology - prevention and control | - |
dc.subject.mesh | Retinal Diseases - physiopathology - prevention and control | - |
dc.subject.mesh | Retinal Vessels - physiology | - |
dc.title | Delayed post-ischemic conditioning significantly improves the outcome after retinal ischemia | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0014-4835&volume=92&issue=6&spage=521&epage=527&date=2011&atitle=Delayed+post-ischemic+conditioning+significantly+improves+the+outcome+after+retinal+ischemia | - |
dc.identifier.email | Marcet, MM: marcet@hku.hk | en_HK |
dc.identifier.authority | Marcet, MM=rp01363 | en_HK |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1016/j.exer.2011.03.015 | en_HK |
dc.identifier.pmid | 21501608 | - |
dc.identifier.pmcid | PMC3833257 | - |
dc.identifier.scopus | eid_2-s2.0-79956363661 | en_HK |
dc.identifier.hkuros | 192920 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-79956363661&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 92 | en_HK |
dc.identifier.issue | 6 | en_HK |
dc.identifier.spage | 521 | en_HK |
dc.identifier.epage | 527 | en_HK |
dc.identifier.eissn | 1096-0007 | - |
dc.identifier.isi | WOS:000291376200012 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Dreixler, JC=6602518830 | en_HK |
dc.identifier.scopusauthorid | Poston, JN=48061473100 | en_HK |
dc.identifier.scopusauthorid | Shaikh, AR=7101736509 | en_HK |
dc.identifier.scopusauthorid | Alexander, M=37025529800 | en_HK |
dc.identifier.scopusauthorid | Tupper, KY=48061583400 | en_HK |
dc.identifier.scopusauthorid | Marcet, MM=8891087900 | en_HK |
dc.identifier.scopusauthorid | Bernaudin, M=6602855984 | en_HK |
dc.identifier.scopusauthorid | Roth, S=7402433182 | en_HK |
dc.identifier.citeulike | 9189158 | - |
dc.identifier.issnl | 0014-4835 | - |