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Prefrontal changes in the glutamate-glutamine cycle and neuronal/glial glutamate transporters in depression with and without suicide

Authors :
S.-F. Gao
D.J. van Wamelen
Paul J. Lucassen
Dick F. Swaab
Xin-Rui Qi
Juan Zhao
Ronald W.H. Verwer
Netherlands Institute for Neuroscience (NIN)
Structural and Functional Plasticity of the nervous system (SILS, FNWI)
Source :
Journal of Psychiatric Research, 82, pp. 8-15, Journal of Psychiatric Research, 82, 8-15, Journal of Psychiatric Research, 82, 8-15. Elsevier B.V., Journal of Psychiatric Research, 82, 8-15. Elsevier
Publication Year :
2016

Abstract

Item does not contain fulltext There are indications for changes in glutamate metabolism in relation to depression or suicide. The glutamate-glutamine cycle and neuronal/glial glutamate transporters mediate the uptake of the glutamate and glutamine. The expression of various components of the glutamate-glutamine cycle and the neuronal/glial glutamate transporters was determined by qPCR in postmortem prefrontal cortex. The anterior cingulate cortex (ACC) and the dorsolateral prefrontal cortex (DLPFC) were selected from young MDD patients who had committed suicide (MDD-S; n = 17), from MDD patients who died of non-suicide related causes (MDD-NS; n = 7) and from matched control subjects (n = 12). We also compared elderly depressed patients who had not committed suicide (n = 14) with matched control subjects (n = 22). We found that neuronal located components (EAAT3, EAAT4, ASCT1, SNAT1, SNAT2) of the glutamate-glutamine cycle were increased in the ACC while the astroglia located components (EAAT1, EAAT2, GLUL) were decreased in the DLPFC of MDD-S patients. In contrast, most of the components in the cycle were increased in the DLPFC of MDD-NS patients. In conclusion, the glutamate-glutamine cycle - and thus glutamine transmission - is differentially affected in depressed suicide patients and depressed non-suicide patients in an area specific way.

Details

ISSN :
00223956
Volume :
82
Database :
OpenAIRE
Journal :
Journal of Psychiatric Research
Accession number :
edsair.doi.dedup.....859f92f13bd513c928e876203661281e
Full Text :
https://doi.org/10.1016/j.jpsychires.2016.06.017