Abstract
Saturation and competition experiments with the radiolabeled β-adrenergic antagonist (-)-[125I]-iodopindolol were used to characterize β-adrenoceptor density (Bmax) and receptor affinity in the extraorbital lacrimal gland of male and female Syrian hamsters. Specific binding to the receptor was saturable. Scatchard analysis of saturation isotherms revealed a single population of receptor sites. Male glands had a significantly higher Bmax (38.9±5.0 vs. 23.3±2.1 fmole/mg protein, -x±SEM, p< 0.02) and receptor affinity (expressed in a lower dissociation constant Kd: 0.065±0.013 vs. 0.120±0.015 nM, p<0.02) than female glands. Binding of the radiolabeled ligand in competition with various adrenergic antagonists showed the receptor to be stereospecific and of the β2-subtype.
Original language | English (US) |
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Pages (from-to) | 153-162 |
Number of pages | 10 |
Journal | Journal of Neural Transmission |
Volume | 77 |
Issue number | 2-3 |
DOIs | |
State | Published - Jun 1989 |
Keywords
- [I]-iodopindolol
- lacrimal gland
- melatonin
- receptor binding
- sexual dimorphism
- β-Adrenoceptor
ASJC Scopus subject areas
- Clinical Neurology
- Neurology
- Psychiatry and Mental health
- Biological Psychiatry