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Adrenoceptors: Receptors, Ligands and Their Clinical Uses, Molecular Pharmacology and Assays.

Jillian Glenda BakerRoger J Summers
Published in: Handbook of experimental pharmacology (2024)
The nine G protein-coupled adrenoceptor subtypes are where the endogenous catecholamines adrenaline and noradrenaline interact with cells. Since they are important therapeutic targets, over a century of effort has been put into developing drugs that modify their activity. This chapter provides an outline of how we have arrived at current knowledge of the receptors, their physiological roles and the methods used to develop ligands. Initial studies in vivo and in vitro with isolated organs and tissues progressed to cell-based techniques and the use of cloned adrenoceptor subtypes together with high-throughput assays that allow close examination of receptors and their signalling pathways. The crystal structures of many of the adrenoceptor subtypes have now been determined opening up new possibilities for drug development.
Keyphrases
  • high throughput
  • single cell
  • induced apoptosis
  • healthcare
  • cell cycle arrest
  • cell therapy
  • oxidative stress
  • signaling pathway
  • mesenchymal stem cells
  • stem cells
  • cell death
  • single molecule
  • case control