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The role of GABA B receptors in depression and antidepressant‐related behavioural responses
Author(s) -
Slattery David A.,
Cryan John F.
Publication year - 2006
Publication title -
drug development research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.582
H-Index - 60
eISSN - 1098-2299
pISSN - 0272-4391
DOI - 10.1002/ddr.20110
Subject(s) - gabab receptor , antidepressant , baclofen , learned helplessness , neuroscience , behavioural despair test , receptor , psychology , pharmacology , gabaa receptor , medicine , agonist , developmental psychology , hippocampus
There is a growing body of clinical evidence that supports a role for a dysfunction of the GABAergic system in mood disorders. Although it is more than 20 years since GABA B receptors were first postulated to play a role in major depression, the initial lack of selective tools hindered further research efforts. In the intervening years, a number of new ligands, including specific GABA B receptor antagonists and positive modulators, as well as genetic tools, GABA B(1) and GABA B(2) receptor knockout mice, have enabled the study of the role of the GABA B receptor in depression and as possible antidepressants. Although initial clinical studies gave rise to the hypothesis that activation of GABA B receptors may induce antidepressant‐like effects, growing evidence suggests that it is in fact GABA B receptor antagonists that have antidepressant‐like potential. This supposition has been reinforced by studies in preclinical models. GABA B receptor antagonists decrease immobility in the forced swim test, in both mice and rats, and also display antidepressant‐like effects in the learned helplessness and chronic mild stress models of depression. While GABA B receptor knockout mice have not been studied to the same extent behaviourally as pharmacological tools, evidence accumulated so far suggests that deletion of either GABA B(1) or GABA B(2) subunits results in antidepressant‐like effects; thus recapitulating data from pharmacological studies. GABA B receptor antagonists have also been shown to increase 5‐HT and dopamine neurotransmission, as well as BDNF levels in numerous brain regions. These systems are all implicated in antidepressant actions and may provide indirect mechanisms by which these compounds display their behavioural effects. Together, accumulating evidence suggests an important role of GABA B receptors in behaviours relevant to depression and that GABA B receptor antagonists may provide clinical benefit in the treatment of depression. Drug Dev Res 67:477–494, 2006. © 2006 Wiley‐Liss, Inc.