Currently, discovery efforts are tending to focus on the different mechanisms for the positive, negative, or cognitive manifestations of schizophrenia.19 Evidence for mechanism(s) of action Human Basic to a full understanding of the biology of the mental dysfunction in psychosis and the therapeutic action of these drugs in psychosis is the concept of the brain as a set of overlapping distributed neural systems, each of which utilizes particular brain regions as needed to fulfill their circuit function. The best understood Inhibitors,research,lifescience,medical set of these distributed systems has been identified using motor out-puts, since motor end points can be most

easily measured in experimental situations.20,21 One set of distributed systems governing aspects of motor function is made up of parallel, this website segregated neuronal circuits that project from the frontal

cortex, supplementary motor area (SMA), to the basal ganglia, and then on to the thalamus, and thereafter return to the SMA. The frontal projections begin Inhibitors,research,lifescience,medical Inhibitors,research,lifescience,medical in the neocortex, synapse in the caudate/putamen, and then split into two pathways, an indirect pathway through the globus pallidus (ultimately inhibitor}’) and a direct pathway to the substantia nigra (ultimately facilitatory), which both pass into the substantia nigra pars reticulata and from there to the specific nuclei of the thalamus. The segregated pathways project from the thalamus back to their specific regions of the frontal cortex, presumably carrying a subcortically modified neuronal signal back Inhibitors,research,lifescience,medical from the basal ganglia to the frontal cortex. D2 dopamine receptors, the putative site of action of antipsychotic drugs, reside in very high concentrations in the caudate and the putamen. Antipsychotic drugs are believed to exert their primary therapeutic action here in the basal ganglia. Yet, a mechanism to transmit this action in the basal ganglia back to the neocortex,

particularly the frontal cortex, would ”deliver“ such a basal ganglia action to Inhibitors,research,lifescience,medical the neocortical brain areas, those presumably affected by schizophrenia. The transmission of this ”D2-receptor-modified“ message through the basal ganglia and thalamus, then back to frontal cortex, is the mechanism that we have proposed to mediate the therapeutic action of these drugs in humans. Indeed, we have tested this hypothesis in our clinical laboratory with next patient volunteers using regional functional imaging techniques with fluorodeoxyglucose (FDG) and positron emission tomography (PET) or regional cerebral blood (rCBF) flow with and without antipsychotic drugs. Simply stated, schizophrenic volunteers received a fixed dose of haloperidol (0.3 mg/kg/day) for 30 days; and then an FDG/PET scan was done. The volunteers then received the same dose of placebo (matched pill number) with a repeat FDG/PET after the second period of 30 days.