Retinal pigment epithelial dystrophy in Briard dogs

Res Vet Sci. 1996 Jan;60(1):17-23. doi: 10.1016/s0034-5288(96)90124-1.

Abstract

The eyes of normal Briard dogs, Briards affected with inherited retinal pigment epithelial dystrophy (RPED) and a range of normal crossbred and beagle dogs were examined and the histopathology of RPED in the Briard was compared with the histopathological features of ageing in the normal canine retina. RPED was characterised by the accumulation of auto-fluorescent lipofuscin-like inclusions in the retinal pigment epithelium (RPE), which initially involved only non-pigmented RPE cells overlying the tapetum but subsequently spread to all pigmented RPE cells. Secondary neuro-retinal degeneration was characterised by a gradual loss of the outer nuclear layer and the subsequent atrophy and degeneration of the inner retina. The loss of primary photoreceptors in the peripheral retina was accompanied by the migration of photoreceptor nuclei and appeared to resemble severe changes due to ageing. Intra-vitreal radiolabelled leucine was used to examine the rate of turnover of the outer segments of the rods in some Briards, but no significant variations were found. The activity of acid phosphatase in RPE was assayed in vitro and showed comparable regional variations in Briard and crossbred dogs. The results suggest that RPED in the Briard is unlikely to be due either to an increased rate of turnover of rod outer segments (and thus an increased phagocytic load) or to a primary insufficiency of lysosomal enzyme.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acid Phosphatase / analysis
  • Aging
  • Animals
  • Dog Diseases*
  • Dogs
  • Microscopy, Fluorescence
  • Pigment Epithelium of Eye / pathology*
  • Retina / growth & development
  • Retina / pathology
  • Retinal Degeneration / pathology
  • Retinal Degeneration / veterinary*
  • Rod Cell Outer Segment / cytology
  • Rod Cell Outer Segment / growth & development
  • Rod Cell Outer Segment / pathology
  • Species Specificity

Substances

  • Acid Phosphatase