According to the World Health Organisation, more than 300 million people worldwide are affected by a major depressive disorder. Unfortunately, the antidepressants commonly used to treat them only work for 50 per cent of the population.
A recent paper published in the journal, Molecular Psychiatry, explores how a protein named CK2 could be playing a key role. The lead author of the paper, Julia Castello, is a biochemistry student at the Graduate Centre, City University of New York (CUNY) working in Eitan Friedman’s neuroscience lab at the City College of New York.
As the research points out, the most used antidepressants are called Selective Serotonin Reuptake Inhibitors (SSRIs). The problem is that there are 14 different types of serotonin receptors, but it is not known which are the mediators of the therapeutic effect of SSRIs. Castello, along with her team, are the first ones to identify CK2 as a modulator of a serotonin receptor, 5-HT4. Manipulation of CK2 in the brain decreases depressive and anxious states through the 5-HT4 receptor.
Castello explained, ‘Identifying new targets broadens our understanding about the cause of depression, as well as the mechanism of action of antidepressants, which could lead to the formulation of new antidepressants that work more efficiently and faster for more people.’
A separate study of CK2’s potential role in Parkinson’s is the subject of another research project at City College. Its findings, published in the Journal of Neuroscience in
December, identify CK2 as a major player in the molecular mechanisms and targets that contribute to modulate L-DOPA induced dyskinesia. L-DOPA is currently the most effective medication available in the market, but a side-effect of this drug is that after years of treatment, patients develop involuntary movements that can be debilitating.