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• W2000668377 abstract "Alterations of GABAergic neurotransmission are assumed to play a crucial role in the pathophysiology of mood disorders. Glutamic acid decarboxylase (GAD) is the key enzyme of GABA synthesis. Immunohistochemical staining of GAD 65/67 was performed in the orbitofrontal, anterior cingulate and dorsolateral prefrontal cortex (DLC), the entorhinal cortex (EC), the hippocampal formation, and the medial dorsal and lateral dorsal thalamic nuclei, with consecutive determination of GAD-immunoreactive (-ir) neuropil relative density. The study was performed on paraffin-embedded brains from 21 depressed patients (14 of whom had committed suicide) and 18 matched controls. The data were tested using Kruskal–Wallis, Mann–Whitney (U) and Spearman statistical procedures. As shown by post-hoc U-tests, an increase in the relative density of GAD-ir neuropil was present in the hippocampal formation, specific for suicidal patients. The EC was the only area where non-suicidal patients also revealed an increase compared with controls. On the contrary, the DLC was the only area where a significant decrease existed, specific for non-suicidal patients. Numerous negative correlations were found between the investigated parameter and psychotropic medication. A major limitation of this study is the relatively small case number. A further limitation is given by the lack of data on drug exposure across the whole life span. The possible impact of unipolar–bipolar dichotomy of mood disorders on the obtained results should also be considered. The study, revealing predominantly an increased relative density of GAD-ir neuropil, suggests the diathesis of GABAergic system specific for depressed suicidal patients." @default.
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• W2000668377 date "2009-02-01" @default.
• W2000668377 modified "2023-10-12" @default.
• W2000668377 title "Suicide and depression in the quantitative analysis of glutamic acid decarboxylase-Immunoreactive neuropil" @default.
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• W2000668377 doi "https://doi.org/10.1016/j.jad.2008.04.021" @default.
• W2000668377 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18538859" @default.
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