Evidence for an hereditary defect in taurine transport in the ciliary epithelium of an inbred strain of rabbits

J Inherit Metab Dis. 1983;6(4):163-6. doi: 10.1007/BF02310874.

Abstract

The concentration of taurine in the aqueous humour and serum of 21 rabbits with hereditary buphthalmia (Bu rabbits-genotype bu/bu) was compared with the aqueous and serum taurine levels of eight strain-related normal rabbits (JAX) and nine non-strain-related normal rabbits (MCV). There was a significant difference in the mean aqueous taurine concentration in each of the three groups. The Bu rabbits had only 29% of the MCV rabbits' level while the JAX rabbits were intermediate with 56% of the MCV level. It is suggested that some of the JAX rabbits may be heterozygous and the Bu rabbits homozygous for a semi-dominant allele of a gene that is less efficient in taurine transport in the ciliary epithelium than the normal allele represented by the MCV animals.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / metabolism*
  • Animals
  • Aqueous Humor / metabolism*
  • Biological Transport
  • Ciliary Body / metabolism
  • Disease Models, Animal*
  • Epithelium / metabolism
  • Glaucoma / congenital*
  • Glaucoma / metabolism
  • Rabbits
  • Taurine / blood
  • Taurine / metabolism*

Substances

  • Taurine