Immunohistochemical distribution of basic fibroblast growth factor in experimental retinal ischaemia and reperfusion in the rat |
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Authors: | Akihiro Ohira Eugene de Juan Jr Yasuo Tano Charles A. Wilson |
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Affiliation: | (1) Department of Ophthalmology, Nagasaki University School of Medicine, 1-7-1, Sakamoto, 852 Nagasaki, Japan;(2) Wilmer Ophthalmological Institute, Johns Hopkins University School of Medicine, 21287 Baltimore, MD, USA;(3) Department of Ophthalmology, Osaka University School of Medicine, 568 Suita, Osaka, Japan;(4) Department of Ophthalmology, University of Texas Southwestern Medical Center at Dallas, 75235-8592 Dallas, TX, USA |
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Abstract: | Summary It has been proposed that basic fibroblast growth factor (basic FGF) mediates the neovascular response in a variety of conditions, including diabetic retinopathy and branch retinal vein occlusion. To test the hypothesis that basic FGF was released from retinal stores as a result of retinal ischaemia, transient retinal ischaemia was induced, followed by 48 h of reperfusion, in the rat by combined central retinal vasculature and optic nerve ligation. The immunolocalization of basic FGF was studied in the retina. We found that basic FGF in the normal retina is present around the deeper retinal vessels and in the neuronal tissue of the outer plexiform layer. In the eyes that had ischaemia followed by reperfusion, there was moderate cellular oedema with retinal swelling, and mitoses in the inner nuclear and plexiform layers. There were no changes evident at the immunohistochemical level either in the intensity or distribution of stores of basic FGF. We conclude from these data that stores of basic FGF are not altered dramatically under the conditions of transient experimental ischaemia and reperfusion in the rat, despite the presence of cellular proliferation. |
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