Structure-Dependent Activity of Natural GABA(A) Receptor Modulators

Molecules. 2018 Jun 22;23(7):1512. doi: 10.3390/molecules23071512.

Abstract

GABA(A) receptors are ligand-gated ion channels consisting of five subunits from eight subfamilies, each assembled in four hydrophobic transmembrane domains. This pentameric structure not only allows different receptor binding sites, but also various types of ligands, such as orthosteric agonists and antagonists, positive and negative allosteric modulators, as well as second-order modulators and non-competitive channel blockers. A fact, that is also displayed by the variety of chemical structures found for both, synthetic as well as nature-derived GABA(A)-receptor modulators. This review covers the literature for natural GABA(A)-receptor modulators until the end of 2017 and discusses their structure-activity relationship.

Keywords: anesthetic; anticonvulsant; anxiolytic; benzodiazepine binding site; natural product; plant origin; sedative; γ-aminobutyric acid.

Publication types

  • Review

MeSH terms

  • Allosteric Regulation
  • Allosteric Site
  • Animals
  • Anti-Anxiety Agents / chemistry*
  • Anti-Anxiety Agents / pharmacology
  • Anticonvulsants / chemistry*
  • Anticonvulsants / pharmacology
  • Catalytic Domain
  • GABA Antagonists / chemistry*
  • GABA Antagonists / pharmacology
  • GABA-A Receptor Agonists / chemistry*
  • GABA-A Receptor Agonists / pharmacology
  • Humans
  • Kinetics
  • Ligands
  • Protein Domains
  • Protein Multimerization
  • Protein Subunits / agonists
  • Protein Subunits / antagonists & inhibitors
  • Protein Subunits / chemistry*
  • Receptors, GABA-A / chemistry*
  • Structure-Activity Relationship

Substances

  • Anti-Anxiety Agents
  • Anticonvulsants
  • GABA Antagonists
  • GABA-A Receptor Agonists
  • Ligands
  • Protein Subunits
  • Receptors, GABA-A