June 1993
Volume 34, Issue 7
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Articles  |   June 1993
Prostaglandin E2 and F2 alpha binding sites in the bovine iris ciliary body.
Author Affiliations
  • S Csukas
    Kentucky Lions Eye Research Institute, University of Louisville School of Medicine 40292.
  • P Bhattacherjee
    Kentucky Lions Eye Research Institute, University of Louisville School of Medicine 40292.
  • L Rhodes
    Kentucky Lions Eye Research Institute, University of Louisville School of Medicine 40292.
  • C A Paterson
    Kentucky Lions Eye Research Institute, University of Louisville School of Medicine 40292.
Investigative Ophthalmology & Visual Science June 1993, Vol.34, 2237-2245. doi:
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    • Get Citation

      S Csukas, P Bhattacherjee, L Rhodes, C A Paterson; Prostaglandin E2 and F2 alpha binding sites in the bovine iris ciliary body.. Invest. Ophthalmol. Vis. Sci. 1993;34(7):2237-2245.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

PURPOSE: To determine the regional distribution and selectivity of prostaglandin E2 (PGE2) and prostaglandin F2 alpha (PGF2 alpha) specific binding sites in membrane preparations from bovine iris ciliary body. METHODS: Bovine eyes were obtained fresh from a local abattoir. Whole irides were separated into sphincter muscle, ciliary body, and remaining iris tissue then homogenized in 50 mM tris buffer, pH 7.5, containing cyclooxygenase, protease, and soybean trypsin inhibitors. Membranes were obtained after three-stage high-speed centrifugation then reconstituted in buffer. Aliquot portions were incubated with 3H-PGE2 or 3H-PGF2 alpha at 37 degrees C for 30 min in a final volume of 500 microliters. Competition studies were performed in the presence of up to 1000-fold excess unlabeled ligand. At the end of a 30-min incubation period, free and membrane bound ligand were separated by rapid filtration through a type HA millipore filter preequilibrated with buffer. The radioactivity bound to the membranes retained on the filter was quantitated in a scintillation counter. RESULTS: The equilibrium dissociation constant and maximum number 3H-PGE2 saturable binding sites were determined by Scatchard analysis. The data best fit to a single binding site model for all three membrane preparations. The majority of the 3H-PGE2 specific binding sites were in sphincter muscle (65%), followed by iris (17%), and ciliary body (18%). 3H-PGE2 alpha binding sites were not measurable in either iris or ciliary body and PGF2 alpha was less competitive than PGE2 in all tissues. The rank order of potency for agonist displacement by both 3H-PGE2 and 3H-PGF2 in sphincter muscle membrane was PGE2 > PGF2 alpha > PGD2 > Iloprost. It was determined that 3H-PGE2 and 3H-PGF2 alpha binding in the bovine sphincter was primarily to EP not FP, DP, or IP prostaglandin receptor types. CONCLUSIONS: The characteristics of PGE2 and PGF2 alpha specific binding sites in the bovine sphincter correlate with its in vitro contractile response to these prostanoids. The inability of PGF2 alpha to effectively compete with PGE2 for specific binding sites in the sphincter and lack of high affinity PGF2 alpha specific binding sites in the iris and ciliary body suggests that this prostaglandin may exert its in vivo effects through PGE2 specific binding sites.

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