To minimize confusion between what is mental and what is physiological, we use the term “neural coordination” to refer specifically to the physiological coordination of neural activity, and we use the term “cognitive coordination” DAPT solubility dmso to refer to interpretations of behavioral observations. The experiments presented here were also formulated within the framework of the discoordination hypothesis, which asserts that disruption of neural coordination produces abnormalities in cognitive coordination, resulting in the core cognitive dysfunctions of schizophrenia.

This physiological hypothesis is agnostic to etiology of the disease and to whether there are abnormalities in dopaminergic, glutamatergic, GABAergic, or other neurotransmitter systems. It is thus remarkable that abnormal synchrony between the two hippocampi was associated with cognitive control difficulties in the adult NVHL rats and that the adolescent cognitive training corrected both the neural and cognitive abnormalities, which confirmed basic predictions of the discoordination hypothesis. We conclude that the present work offers an experimental platform for evaluating both the neurodevelopmental

and discoordination hypotheses. An important next step is to use the platform to evaluate other neurodevelopmental schizophrenia models with distinct Selleck ABT 263 etiologies such as the drug-induced methylazoxymethanol (MAM) model (Chen and Hillman,

1986; Featherstone et al., 2007), the polyriboinosinic-polyribocytidilic acid (PolyI:C) immune challenge model (Meyer et al., 2005; Pearce, 2001), and genetic models, such as the DISC1 (Kim et al., 2012) and other mutant mouse models (Belforte et al., 2010; Sigurdsson et al., 2010). The benefits Ketanserin of early cognitive training demonstrated in the NVHL model indicate the possibility of a critical window for procognitive intervention in schizophrenia and related disorders. This offers preclinical support for the idea that it is more effective to treat schizophrenia patients in the prodrome of the disease, at the very earliest signs of a disorder (Bird et al., 2010; Lieberman et al., 2001; Perkins et al., 2005). In fact, the present findings suggest that there may be substantial merit to explore the effectiveness of behavioral interventions even earlier in a preemptive effort. While further work in animal models will be needed to define and possibly expand (Maya Vetencourt et al., 2008) the boundaries of the opportunity, adolescence may be a natural target since it is characterized by substantial brain maturation (Shen et al., 2010; Uhlhaas et al., 2009; Yurgelun-Todd, 2007). The mechanism for the increase of interhippocampal synchrony we observed in the adolescent-trained NVHL rats is unknown and may be multifaceted.