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This article is part of the supplement: Seventeenth Annual Computational Neuroscience Meeting: CNS*2008

Open Access Poster presentation

Roles of prefrontal cortical GABAergic interneurons in psychosis and cognitive deficits in schizophrenia

Shoji Tanaka

Author Affiliations

Dept. of Information & Communication Science, Sophia University, Tokyo 102-8554, Japan

BMC Neuroscience 2008, 9(Suppl 1):P36  doi:10.1186/1471-2202-9-S1-P36

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2202/9/S1/P36


Published:11 July 2008

© 2008 Tanaka; licensee BioMed Central Ltd.

Clinical background

Analysis of postmortem brains of patients with schizophrenia from the Stanley Foundation brain collection have shown consistent reduction of reelin, parvalbumin and GAD67, the 67-kilodalton isoform of glutamic acid decarboxylase, in the prefrontal cortex (PFC) and other brain regions [1]. In the PFC, this suggests a decrease in GABAergic inhibition that might be responsible for psychosis. Cognitive deficits are also a core symptom of schizophrenia, which might also be caused by GABAergic dysregulation.

Results

The PFC circuit of pyramidal neurons and GABAergic chandelier neurons and other GABAergic neurons is implemented with a firing rate model. The dopaminergic modulation of the neuronal activity via D1 receptor activation is essentially the same as in the previous model [2]. Figure 1 shows the time courses of dopaminergic modulation profiles of the pyramidal neurons with different sets of the strength of GABAergic inhibition (see table 1). Without chandelier neurons, hyperactive states readily emerge. Weaker inhibition by other GABAergic neurons enlarges the inverted-U shaped profile to connect it to the hyperactive profile.

Table 1. A summary of the variations of the parameter values of the two different types of GABAergic inhibition used in the simulation. The figures in the parentheses indicate the relative strength of the inhibitory action on the pyramidal neurons in the model PFC circuit.

thumbnailFigure 1. Three-dimensional representations of DA modulatory landscapes with (B) and without (A, C, and D) chandelier neurons. Note that the onset of the hyperactive mode is very quick (less than 100 ms), whereas the inverted-U mode profiles are very slow to evolve. Even at t = 1000 ms, the profiles of the inverted-U mode have not reached the equilibrium states.

Conclusion

Both chandelier neurons and other GABAergic neurons play critical roles in shaping the dopaminergic modulation profile of PFC activity. Chandelier neurons would suppress hyperactivity with hyper-dopaminergic neurotransmission, which is associated with psychotic states. Other GABAergic neurons regulate the inverted-U shaped profile with moderate levels of dopaminergic neurotransmission, which is important for normal cognitive functions.

References

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