1. Iron in hereditary retinal degeneration: PIXE microanalysis
- Author
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Marina Yefimova, Y Llabador, J.C. Jeanny, Yves Courtois, M. Simonoff, C Sergeant, and Barbara Gouget
- Subjects
chemistry.chemical_classification ,Retinal degeneration ,Nuclear and High Energy Physics ,Pathology ,medicine.medical_specialty ,Retina ,genetic structures ,Chemistry ,business.industry ,chemistry.chemical_element ,Retinal ,Calcium ,medicine.disease ,Microanalysis ,eye diseases ,Staining ,chemistry.chemical_compound ,Optics ,medicine.anatomical_structure ,Transferrin ,medicine ,Immunohistochemistry ,sense organs ,business ,Instrumentation - Abstract
Several types of hereditary retinal degeneration with progressive alteration of photoreceptors exist in men and animals. Recent immunohistochemical results have shown strong degradation of transferrin, the protein responsible for iron transport, in retinas of rats with hereditary retinal degeneration. Freeze-dried thin sections of rat retinas from different stages of the disease, and respective coeval control sections, have been analyzed using nuclear microprobe. In this first part of the study, the rat retinas at post-natal stages of 35 and 45 days have been analyzed. The sample preparation and the post-irradiation staining to determine precisely the retinal layers involved are described. Preliminary results of element distributions (K, Ca, Fe) in the rat retina layers are discussed. A very high content of calcium in the choriocapillaris of dystrophic rat retinas was observed. Preliminary results on iron distribution in the rat retina layers are presented.
- Published
- 1999
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