Journal of Ocular Pharmacology and Therapeutics · 1993 · 19 citations · 12 references
MedicineEndocrinologyPharmacologyHormone BiochemistryMolecular PharmacologyNeuroendocrinologyEndocrine PharmacologyHormone Binding ProteinsHormone ReceptorsLigand BindingReceptor PharmacologyBinding Affinity MeasurementsExocrine OrgansHormone Binding AffinityHormone Receptor PharmacologyLacrimal Gland FunctionLacrimal Gland InnervationRadioligand Binding AssaysScatchard Analysis
Applying the technic of S.A. Wolfe et al. [Endocrinology, 124, 1160-1172, 1989], we have established the presence of sigma receptors in isolated, but intact, lacrimocytes excised from main lacrimal gland tissue of the New Zealand white rabbit. 3H-Haloperidol was used as the ligand (0.5-2500 nM), in the presence of spiperone. From a Scatchard plot, a single binding site was statistically chosen over two sites for a majority of the data associated with the intact lacrimocytes. Kd (71.0 +/- 46.4 nM) and Bmax (588.2 +/- 166.7 fmol/mg of protein) values showed lower binding affinity but a similar density of sigma sites in rabbit lacrimocytes when compared to published results obtained for rat exocrine glands and brain tissue. Using the technic of McCann and Su [J. Pharm. Exp. Therap., 257, 547, 1991], membrane suspensions of the sigma receptor were also prepared and tested for binding to radioligands, 3H-DTG, as well as 3H-haloperidol. A Scatchard plot revealed two binding sites for 3H-DTG and one binding site for 3H-haloperidol. The high affinity site for 3H-DTG yielded a Kd of 1.04 +/- 0.64 nM, whereas, Bmax was 135.9 +/- 11.62 fmol/mg of protein. The low affinity site gave a Kd = 75.3 +/- 26.8 nM and Bmax = 344.0 +/- 222.0 fmol/mg of protein. The weaker site is suspected to be intracellular. IC50 values were determined for N,N-disubstituted arylphenylalkylamines (Kd approximately low nM).
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