Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1994 Apr;232(4):232-7.
doi: 10.1007/BF00184011.

Impact of lipofuscin on the retinal pigment epithelium: electroretinographic evaluation of a protease inhibition model

Affiliations

Impact of lipofuscin on the retinal pigment epithelium: electroretinographic evaluation of a protease inhibition model

L M Rapp et al. Graefes Arch Clin Exp Ophthalmol. 1994 Apr.

Abstract

With aging, the retinal pigment epithelium (RPE) becomes increasingly congested with residual debris called lipofuscin. Little is known about the impact of lipofuscin on retinal function, and this was addressed in the present study by examining the influence of RPE debris on electroretinographic (ERG) parameters utilizing an experimental model of lipofuscin accumulation. Pigmented rats were injected intravitreally with the protease inhibitor leupeptin, and examined 1 week later by electroretinogram (ERG) recording and light and electron microscopy. Relative to vehicle-injected controls, leupeptin-treated retinas showed abundant accumulation throughout the RPE cytoplasm of inclusions that resembled lipofuscin. RPE cells filled with this debris showed a marked increase in height and a displacement of melanin from their apical border. Morphological changes in the RPE had no influence on retinal function since ERG threshold, a- and b-wave maximum amplitude, latency and implicit time were not significantly different between leupeptin-treated eyes and controls. Furthermore, leupeptin-induced RPE inclusions did not alter either the rate or extent of ERG dark adaptation. These findings suggest that filling of the RPE cytoplasm with residual debris is not in itself likely to be the cause of functional alterations in the aging eye.

PubMed Disclaimer

Similar articles

References

    1. Am J Ophthalmol. 1990 Mar 15;109(3):265-78 - PubMed
    1. Invest Ophthalmol Vis Sci. 1992 Dec;33(13):3497-9 - PubMed
    1. Nature. 1993 Feb 25;361(6414):724-6 - PubMed
    1. Invest Ophthalmol Vis Sci. 1976 Sep;15(9):700-25 - PubMed
    1. Nature. 1960 Oct 8;188:114-8 - PubMed

Publication types