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Altered organization of GABAA receptor mRNA expression in the depressed suicide brain

Authors :
Hymie Anisman
Michael O. Poulter
Miklós Palkovits
Gabor Faludi
Lisheng Du
Vladimir Zhurov
Zul Merali
Source :
Frontiers in Molecular Neuroscience, Vol 3 (2010), Frontiers in Molecular Neuroscience
Publication Year :
2010
Publisher :
Frontiers Media SA, 2010.

Abstract

Inter-relationships ordinarily exist between mRNA expression of GABA-A subunits in the frontopolar cortex (FPC) of individuals that had died suddenly from causes other than suicide. However, these correlations were largely absent in persons that had died by suicide. In the present investigation, these findings were extended by examining GABA-A receptor expression patterns (of controls and depressed individuals that died by suicide) in the orbital frontal cortex (OFC), hippocampus, amygdala. locus coeruleus (LC),and paraventricular nucleus (PVN), all of which have been implicated in either depression, anxiety or stress responsivity. Results Using QPCR analysis, we found that in controls the inter-relations between GABA-A subunits varied across brain regions, being high in the hippocampus and amygdala, intermediate in the LC, and low in the OFC and PVN. The GABA-A subunit inter-relations were markedly different in persons that died by suicide, being reduced in hippocampus and amygdala, stable in the LC, but more coordinated in the OFC and to some extent in the PVN. Conclusions It seems that altered brain region-specific inhibitory signaling, stemming from altered GABA-A subunit coordination, are associated with depression/suicide. Although, it is unknown whether GABA-A subunit re-organization was specifically tied to depression, suicide, or the accompanying distress, these data show that the co-ordinate expression of this transcriptome does vary depending on brain region and is plastic.

Details

ISSN :
16625099
Volume :
3
Database :
OpenAIRE
Journal :
Frontiers in Molecular Neuroscience
Accession number :
edsair.doi.dedup.....c8cef26e36a0ca770c97b8615e336c81
Full Text :
https://doi.org/10.3389/neuro.02.003.2010