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Parvalbumin neurons in the entorhinal cortex of subjects diagnosed with bipolar disorder or schizophrenia

Journal

BIOLOGICAL PSYCHIATRY
Volume 61, Issue 5, Pages 640-652

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2006.04.026

Keywords

bipolar disorder; entorhinal cortex; immunocytochemistry; parvalbumin; postmortem; schizophrenia

Funding

  1. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH066955, R24MH068855, P50MH060450, R03MH063215] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS037483] Funding Source: NIH RePORTER
  3. NIMH NIH HHS [MH063215, R01 MH066955, MH06628, R24 MH068855, P50 MH060450, R24MH068855, MH60450] Funding Source: Medline
  4. NINDS NIH HHS [NS37483, R01 NS037483] Funding Source: Medline

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Background: Growing evidence indicates that the entorhinal cortex (ECx) might be affected in schizophrenia (SZ) and bipolar disorder (BD). To test whether distinct interneuronal subpopulations might be altered, numbers of parvalburnin-immunoreactive (PVB-IR) neurons were measured in the ECx of BD and SZ subjects. These neurons play a pivotal role within ECx intrinsic circuits. Methods: Numbers, numerical density, and soma size of PVB-IR neurons were measured in the ECx of normal control (n = 16),BD(n = 10), and SZ (n = 10) subjects. The volume of the ECx was measured in Nissl-stained sections. Results: In 131), decreases of total numbers (p = .02) and numerical densities (p = .01) of PVB-IR neurons were detected in the ECx. Within distinct subregions, reductions were detected in the superficial layers of the lateral (p = .02), intermediate (p = .04), and caudal (p = .01) ECx. In SZ, total numbers and numerical densities were not altered. A reduction of soma size was present in the intermediate ECx (P = .01). Volume was unaffected in either disorder. Conclusions: In 131), a decrease of PVB-IR neurons may alter intrinsic inhibitory networks within the superficial layers of the ECx. The likely consequence is a disruption of integration and transfer of information from the cerebral cortex to the hippocampus.

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