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Updated: Oct 13, 2026

Methods for the Discovery of Novel Compounds Modulating a Gamma-Aminobutyric Acid Receptor Type A Neurotransmission
Published on: August 16, 2018
[How far has the search for endogenous ligands of benzodiazepine receptors progressed?]
Abstract:
The discovery, in 1977, of the specific binding sites for benzodiazepines in the brain of mammals, notably in man, lends support to the possible existence of endogenous compounds acting as natural ligands of these sites. At present, a dozen of molecules having the capacity to displace bound 3H-benzodiazepines from their specific sites have been extracted from the brain of several species (rat, pig, bovine...), the cerebrospinal fluid and urine of man. These molecules are proteins, peptides, purines, beta-carbolines... and exhibit (some) pharmacological properties similar or opposite to those of benzodiazepines. The most recent data concerning benzodiazepine receptors suggest that the endogenous ligand would be, if it exists, a benzodiazepine-like compound (agonist) with an indolic structure.
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