205 Another recent study found that olanzapine increased NAA in the selleck inhibitor prefrontal cortex of remitted adolescent patients with mania compared with nonremitted patients.206 Although this suggests a possible in vivo neurotrophic effect, this finding needs further replication because the primary aim of the study – a NAA increase following olanzapine treatment, independent from clinical change – was negative. In fact, it is possible that the Inhibitors,research,lifescience,medical NAA increase seen in responders was more closely related to improved mood than to olanzapine’s neurotrophic properties. Closing remarks The growing data from molecular, cellular,

animal, and human studies described in this review support Inhibitors,research,lifescience,medical the notion that psychotropic agents used to treat the major psychiatric disorders – especially mood stabilizers – are associated with significant

neurotrophic/neuroprotective effects. These effects may enhance cellular resilience and plasticity in dysfunctional synapses and neural circuitry implicated in psychiatric disorders. The crux of such research is that, in addition to their proven Inhibitors,research,lifescience,medical ability to treat psychiatric disorders, these agents may be useful in the treatment of neurodegenerative illnesses and ischemia. Similarly, psychotropic agents developed for the treatment of neurodegenerative illnesses may be beneficial as therapeutics for major psychiatric illnesses. Currently, several Inhibitors,research,lifescience,medical clinical trials are being conducted to evaluate the feasibility of using the following site lithium and valproate to treat a variety of neurodegenerative diseases. Indeed, neuroprotection is the most consistent biological outcome associated with lithium treatment. There is hope that these Inhibitors,research,lifescience,medical clinically safe and widely used agents will

slow disease progression, and perhaps produce functional improvements. Furthermore, because lithium and valproate stimulate the ERK and PI3K pathways, increase BDNF, Bcl-2, and BAG-1 expression, block HDAC activity (valproate only), and inhibit GSK-3 alpha and beta activities, continued study of these agents may elucidate other clinically relevant targets, ultimately leading to improved treatments for these devastating disorders. Additional data are also needed to understand whether the neurotrophic and neuroprotective effects of mood stabilizers, antidepressants, and antipsychotics are cell-type or circuitry Cilengitide specific, and to what extent their neurotrophic/neuroprotective effects contribute to their therapeutic action. Finally, gaining insight into rapid-acting versus long-term compensatory changes facilitated by these psychotropic agents will pave the way for the next generation of therapeutics, whose dual nature will provide both a rapid treatment response to restore function, as well as support long-term changes to maintain successful treatment and prevent relapse.