OPIATE BINDING-SITES IN THE RETINA - PROPERTIES AND DISTRIBUTION
- 1 January 1980
- journal article
- research article
- Vol. 215 (1) , 60-64
Abstract
The presence of opiate binding sites in rat retina was confirmed and their properties and distribution were investigated. Etorphine, naloxone and methionine enkephalin exhibit high affinity, saturable binding to retinal membrane preparations. Scatchard analysis of the binding data yielded linear plots for each ligand. The P1 subcellular fraction contains the greatest density of sites/mg of protein. The response of the binding of all ligands to Na ions was similar in the retina to that observed in the brain. Competition experiments using naloxone and methionine enkephalin indicated that a homogeneous class of binding sites exists in the rat retina. Opiate binding sites were demonstrated in the retina of cow, foad and skate. Methionine enkephalin-like immunoreactivity was not clearly detectable in rat retina, but was present in toad retina. The physiological role of the opiate binding sites in the retina remains to be elucidated.This publication has 16 references indexed in Scilit:
- Subcellular distribution of GABA receptors in bovine retinaExperimental Eye Research, 1979
- Distribution of methionine- and leucine-enkephalin within the rat pituitary gland measured by highly specific radioimmunoassaysBiochemical and Biophysical Research Communications, 1978
- Different Brain Areas Mediate the Analgesic and Epileptic Properties of EnkephalinScience, 1978
- The opiate receptor binding interactions of 3H-methionine enkephalin, an opioid peptideEuropean Journal of Pharmacology, 1978
- Uptake and release of [14C]GABA from rabbit retina synaptosomesExperimental Eye Research, 1977
- Endogenous opioid peptides: multiple agonists and receptorsNature, 1977
- Isolation, primary structure, and synthesis of α-endorphin and γ-endorphin, two peptides of hypothalamic-hypophysial origin with morphinomimetic activityProceedings of the National Academy of Sciences, 1976
- Opioid activity of a peptide, beta-lipotropin-(61-91), derived from beta-lipotropin.Proceedings of the National Academy of Sciences, 1976
- EFFECTS OF MORPHINE-LIKE AND NALORPHINE-LIKE DRUGS IN NONDEPENDENT, MORPHINE-DEPENDENT AND CYCLAZOCINE-DEPENDENT CHRONIC SPINAL DOG1976
- EFFECTS OF MORPHINE-LIKE AND NALORPHINE-LIKE DRUGS IN NONDEPENDENT AND MORPHINE-DEPENDENT CHRONIC SPINAL DOG1976