Targeting glycogen synthase kinase-3 as an approach to develop novel mood-stabilising medications

Abstract

Historically, success in the pharmacological treatment of bipolar disorder has arisen either from serendipitous findings or from studies with drugs (antipsychotics and anticonvulsants) developed for other indications (schizophrenia and epilepsy, respectively). Lithium has been in widespread clinical use in the treatment of bipolar disorder for > 30 years. Development of lithium-mimetic compounds has the potential to result in a more specific medication, with fewer side effects and a less narrow dose range. However, novel medications based upon a known mechanism of action of this drug are yet to be developed. Increasing evidence suggests that a next-generation lithium compound may derive from knowledge of a direct target of lithium, glycogen synthase kinase-3 (GSK-3). GSK-3 is an intracellular enzyme implicated as a critical component in many neuronal signalling pathways. However, despite the large body of preclinical data discussed in this review, definitive validation of GSK-3 as therapeutically relevant target of lithium will require clinical trials with novel GSK-3 inhibitors. A number of recent reports suggest that it is possible to develop selective, small-molecule GSK-3 inhibitors.

Keywords::

• antidepressant
• bipolar disorder
• depression
• kinase inhibitor
• mania
• manic-depressive illness
• mood stabiliser

Acknowledgements

Research supported by the Intramural Research Programme of the National Institute of Mental Heath and the National Association for Research on Schizophrenia and Depression (Young Investigator Award). This manuscript benefited from the comments of Drs Kelley O’Donnell, Guang Chen and Husseini Manji.

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