Because of their anxiolytic, sedative and myo-relaxant properties, ben
zodiazepines are among the most commonly used drugs in clinical practi
ce. The actions of benzodiazepines are mediated by two classes of rece
ptors i.e. receptors associated with the GABA(A-) chloride channel com
plex also named central-type benzodiazepine receptors and receptors lo
calized in the mitochondrial membrane called peripheral-type benzodiaz
epine receptors. The existence of binding sites for benzodiazepines ha
s suggested the existence of endogenous ligands capable of interacting
with either central or peripheral type benzodiazepine receptors. This
hypothesis has led to the dicovery of a family of regulatory peptides
named endozepines which displace diazepam from its neuronal binding s
ites and exert a wide range of biological activities.