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Are dopamine receptors present on human lymphocytes?
The Journal of Pharmacy and Pharmacology
|October 1, 1982
Summary
Researchers investigated [3H] spiperone binding in human lymphocytes. Findings suggest passive uptake, not dopamine receptors, causes ligand association with these cells.
Area of Science:
- Immunology
- Neuropharmacology
Background:
- Human lymphocytes are investigated for potential dopamine receptor expression.
- The radioligand [3H] spiperone is commonly used to study dopamine D2 receptors.
Purpose of the Study:
- To characterize the binding of [3H] spiperone to human lymphocytes.
- To determine if dopamine receptors are present on the surface of human lymphocytes.
Main Methods:
- Incubation of human lymphocytes with [3H] spiperone.
- Competition binding assays using various drugs, including dopamine-active agents and isomers of butaclamol.
- Cell fragmentation and lysis experiments.
- Investigation of binding under conditions affecting active transport (iodoacetate, ion replacement).
Main Results:
- [3H] spiperone binding to lymphocytes was not saturable and lacked stereoselectivity.
- No correlation was found between the dopaminergic activity of drugs and their ability to displace the ligand.
- Chloroquine, a non-dopaminergic drug, was a potent displacer.
- Cell fragmentation and lysis significantly reduced ligand binding.
- Binding was unaffected by metabolic inhibitors or ion substitution, indicating a passive process.
Conclusions:
- The observed association of [3H] spiperone with human lymphocytes is likely due to passive cellular uptake, not specific receptor binding.
- Evidence does not support the existence of dopamine receptors on the surface of human lymphocytes.
- Further research is needed to elucidate the mechanisms of passive ligand accumulation in lymphocytes.