Guanabenz, guanochlor, guanoxan and idazoxan bind with high affinity to non-adrenergic sites in pig kidney membranes

Eur J Pharmacol. 1989 Jan 31;160(2):295-8. doi: 10.1016/0014-2999(89)90503-7.

Abstract

[3H]Idazoxan is a labelled ligand that is frequently used to study alpha 2-adrenoceptors in the central nervous system. In pig kidney membranes, [3H]idazoxan labelled high-affinity binding sites (Kd = 1.5 nM) that were not alpha 2-adrenoceptors and which recognized clonidine with low affinity. This new class of binding sites was recognized by amiloride derivatives; however, it is not likely that these sites are the well-known targets of amiloride in the kidney: the Na+/H+ exchanger and the epithelium Na+ channel. These binding sites may be the normal target of a series of imidazolidines derivatives (guanabenz, guanochlor, guanoxan), which are known for their antihypertensive properties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amiloride / metabolism
  • Animals
  • Antihypertensive Agents / metabolism*
  • Binding, Competitive
  • Cell Membrane / metabolism
  • Dioxanes / metabolism
  • Guanabenz / metabolism
  • Guanidines / metabolism
  • Idazoxan
  • In Vitro Techniques
  • Kidney / metabolism*
  • Receptors, Adrenergic / metabolism
  • Swine

Substances

  • Antihypertensive Agents
  • Dioxanes
  • Guanidines
  • Receptors, Adrenergic
  • Amiloride
  • Guanabenz
  • guanoclor
  • Idazoxan