Photoreceptor rescue after low-dose intravitreal IL-1β Injection in the RCS Rat

Photoreceptor survival in the dystrophic rat was evaluated following administration of IL-1β at dosages much lower than those used previously for this purpose. Royal College of Surgeons rats (pink-eyed, pigmented, or non-dystrophic) received 1μ l intravitreal injections of murine recombinant IL-1β (...

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Veröffentlicht in:Experimental eye research 2001-10, Vol.73 (4), p.557-568
Hauptverfasser: Whiteley, Simon J.O, Klassen, Henry, Coffey, Peter J, Young, Michael J
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Sprache:eng
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Zusammenfassung:Photoreceptor survival in the dystrophic rat was evaluated following administration of IL-1β at dosages much lower than those used previously for this purpose. Royal College of Surgeons rats (pink-eyed, pigmented, or non-dystrophic) received 1μ l intravitreal injections of murine recombinant IL-1β (0.5, 2, or 5μ gml−1; at 3 or 4 weeks of age). Eyes were harvested 4 weeks later and outer nuclear layer profiles counted. Additional animals received intravitreal basic fibroblast growth factor (1000μ gml−1), or vehicle alone. Others were treated with IL-1β to evaluate the inflammatory response (CD45+ profiles) or visual function via opto-kinetic response. IL-1β was associated with photoreceptor rescue that was both dose-dependent and comparable to that seen following high-dose basic fibroblast growth factor. Significant anatomical rescue relative to controls was seen in both pink-eyed and pigmented strains, although the degree and distribution varied between strains. Functional rescue was confirmed by opto-kinetic response using the pigmented strain. At 5μ gml−1, IL-1β resulted in numerous CD45+ profiles within the retina and vitreous. Infiltration peaked at 48hr and was minimal at 4 weeks, without dysplastic sequelae. IL-1β therefore induces visually significant photoreceptor rescue in a potent, dose-dependent manner that need not entail cytoarchitectural disruption. This is consistent with the known association between injury and rescue in the rat retina. Neuroprotection may be a general, if under-appreciated, consequence of inflammatory cascade activation.
ISSN:0014-4835
1096-0007
DOI:10.1006/exer.2001.1066