Article révisé par les pairs
Résumé : α2- Adrenergic receptors were identified in calf brain, human platelet and human uterus membranes by [3H]-rauwolscine binding.The reagents phenylglyoxal (selective for guanidino groups), p- hydroxy mercuribenzoate and N-ethylmaleimide (selective for sulfhydryl groups) caused a time- and dose- dependent decrease in the number of receptor sites. α2-Adrenergic agonists and antagonists mediated efficient protection of the receptors against these reagents. These data suggest that essential arginine and cysteine residues are present at or near the α2-adrenergic binding site. © 1985.