Source:http://linkedlifedata.com/resource/pubmed/id/19250642
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2009-3-9
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pubmed:abstractText |
Retinal leukostasis, mediated by intracellular adhesion molecule-1 (ICAM-1) and vascular endothelial growth factor (VEGF), has been implicated in the pathogenesis of early diabetic retinopathy. Phosphomannopentaose sulfate (PI-88) is a highly sulfonated oligosaccharide which inhibits heparanase activity and competes with heparan sulfate binding to growth factors. In this study, we evaluated whether PI-88 could inhibit retinal leukostasis in strepotzotocin(STZ)-induced diabetic rat and elucidated the possible mechanisms. Diabetes was induced in Sprague-Dawley rats by intraperitoneal injection (i.p.) of STZ. Three months after induction, diabetic rats were administered PI-88 (25 mg/kg body weight) or vehicle solution daily via i.p. for 14 consecutive days. Leukostasis was analyzed on retinal flatmounts by concanavalin A and CD45 immunofluorescence staining. Retinal function was analyzed by electroretinography (ERG). ICAM-1 and VEGF levels in retinas were studied by Western blot and enzyme-linked immunosorbent assay (ELISA) respectively. The systemic administration of PI-88, but not vehicle, significantly decreased the number of adherent leukocytes in retinas by 52.24% (P<0.001) and led to significant preservation (about 50%, P<0.001) of scotopic ERG a- and b-wave amplitudes in treated diabetic rats as compared to those of diabetic control rats. These changes were associated with downregulation of ICAM-1 (45%, P<0.001) and VEGF (26.83+/-2.01 versus 40.8+/-3.24 pg/mg, P<0.01) in retinas of PI-88 treated diabetic rats as compared to those of diabetic control rats. PI-88 significantly inhibited retinal leukostasis and reversed retinal dysfunction by a mechanism that may include decreased ICAM-1 and VEGF expression in diabetic rats. Our data suggests that PI-88 is a promising agent for the treatment of diabetic retinopathy.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Adhesion Molecule-1,
http://linkedlifedata.com/resource/pubmed/chemical/Oligosaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/Vascular Endothelial Growth Factor A,
http://linkedlifedata.com/resource/pubmed/chemical/phosphomannopentaose sulfate,
http://linkedlifedata.com/resource/pubmed/chemical/vascular endothelial growth factor...
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1090-2104
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
6
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pubmed:volume |
380
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
402-6
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pubmed:meshHeading |
pubmed-meshheading:19250642-Animals,
pubmed-meshheading:19250642-Diabetes Mellitus, Experimental,
pubmed-meshheading:19250642-Diabetic Retinopathy,
pubmed-meshheading:19250642-Down-Regulation,
pubmed-meshheading:19250642-Electroretinography,
pubmed-meshheading:19250642-Injections, Intraperitoneal,
pubmed-meshheading:19250642-Intercellular Adhesion Molecule-1,
pubmed-meshheading:19250642-Leukostasis,
pubmed-meshheading:19250642-Oligosaccharides,
pubmed-meshheading:19250642-Rats,
pubmed-meshheading:19250642-Rats, Sprague-Dawley,
pubmed-meshheading:19250642-Retina,
pubmed-meshheading:19250642-Vascular Endothelial Growth Factor A
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pubmed:year |
2009
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pubmed:articleTitle |
Phosphomannopentaose sulfate (PI-88) inhibits retinal leukostasis in diabetic rat.
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pubmed:affiliation |
State Key Laboratory of Ophthalmology, Zhongshan Opthalmic Center, Sun Yat-sen University, 54S, Xianlie Road, Guangzhou 510060, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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