Isolation of an endogenous clonidine‐displacing substance from rat brain

Abstract

An endogenous substance which specifically displaces clonidine, yohimbine and rauwolscine from rat brain α₂-adrenergic receptors, has been isolated. The new compound, designed clonidine-displacing-substance (CDS), has been partially purified by ion exchange chromatography, zone electrophoresis and high performance liquid chromatography (HPLC). CDS binds specifically to α₂-adrenergic receptors by competing with either α₂-adrenergic agonists or α₂-antagonists, but has no effect on the specific binding of [³H]prazosin to α₁-adrenergic receptors in rat brain membranes. In the course of isolation, CDS was shown to be neither the endogenous neurotransmitter (−)norepinephrine (NE) nor the guanyl nucleotide GTP which lowers the specific binding of α₂-agonists to the α₂-adrenergic receptors.