Binding characteristics of 3H-prazosin to rat brain alpha-adrenergic receptors

Eur J Pharmacol. 1979 May 1;55(3):323-6. doi: 10.1016/0014-2999(79)90202-4.

Abstract

3H-Prazosin binding to membranes from rat brain is saturable, Bmax, 77 fmol/mg protein, of high affinity, KD, 0.28 nM and with a drug specificity indicating that it labels alpha-adrenergic receptors. The ranking of alpha-antagonists for these binding sites suggests that 3H-prazosin may be useful in identifying a subpopulation of alpha-receptors (alpha1) in the central nervous system.

MeSH terms

  • Adrenergic alpha-Agonists / metabolism
  • Adrenergic alpha-Antagonists / metabolism
  • Animals
  • Brain / metabolism*
  • In Vitro Techniques
  • Male
  • Membranes / metabolism
  • Prazosin / metabolism*
  • Protein Binding
  • Quinazolines / metabolism*
  • Rats
  • Receptors, Adrenergic / metabolism*
  • Receptors, Adrenergic, alpha / metabolism*

Substances

  • Adrenergic alpha-Agonists
  • Adrenergic alpha-Antagonists
  • Quinazolines
  • Receptors, Adrenergic
  • Receptors, Adrenergic, alpha
  • Prazosin