159 The close link between the clock machinery and core metabolic cellular processes is confirmed by the study of protein modulators such as glycogen synthase kinase 3β (GSK3-β), which is a core constituent of the mammalian circadian clock and affects circadian rhythm generation by modifying the stability of circadian clock molecules.160 This kinase is also an essential element of the Wnt/beta-catenin pathway, which is involved in the control of gene expression, cell behavior,

cell adhesion, and cell polarity, and plays major roles in neurodevelopment and in regulation of neuronal polarity, #learn more keyword# neuronal plasticity, and

cell survival.161 It regulates the activity of many targets including transcriptional factors, enzymes, and cytoskeletal proteins,162 Inhibitors,research,lifescience,medical and is considered a primary regulator in a range of cellular processes including differentiation, growth, motility, and apoptosis.163 GSK-3 influences the susceptibility of neurons to harmful stimuli (neuronal resilience), because increasing GSK-3 activity increases Inhibitors,research,lifescience,medical apoptosis in neuronal cells, while inhibiting GSK has neuroprotective effects,164 and because its inhibition occurs in response to brain-derived neurotrophic factor (BDNF)

Inhibitors,research,lifescience,medical and other neurotrophins.165 These mechanisms provide a target for the convergent effects of chronotherapeutics and antidepressant drugs on the biological clock and on neurotransmitter systems. Control of the phosphorylation/activity status of GSK3β is considered an important mechanism of serotonin Inhibitors,research,lifescience,medical (5-HT) and dopamine (DA) action on brain and behavior,166 because GSK3-β is inhibited by lithium, valproate, and several antidepressants such as selective serotonin reuptake inhibitors, monoamine oxidase inhibitors, and tricyclic antidepressants.165,167 Confirming the role of these mechanisms for bipolar disorder and chronotherapeutics, promoter gene secondly variants were associated with less detrimental clinical features, including a delayed onset of illness,168 a better clinical response to lithium,169,170 and a better response to sleep deprivation171: this effect was so strong as to overcome the detrimental influence on SD response of genotypes negatively affecting serotonergic function. 111,172 Molecular mechanisms involved in brain plasticity are likely to play a major role in antidepressant response and long-term mood stabilization of bipolar patients.