Brain metabolic derangements examined using 1H MRS and their (in)consistency among different rodent models of depression
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, přehledy, práce podpořená grantem
PubMed
37301420
DOI
10.1016/j.pnpbp.2023.110808
PII: S0278-5846(23)00094-5
Knihovny.cz E-zdroje
- Klíčová slova
- Animal models, Depression, Metabolites, Proton magnetic resonance spectroscopy,
- MeSH
- deprese MeSH
- depresivní porucha unipolární * metabolismus MeSH
- glutamin * metabolismus MeSH
- hlodavci metabolismus MeSH
- kyselina asparagová metabolismus MeSH
- kyselina glutamová metabolismus MeSH
- mozek metabolismus MeSH
- protonová magnetická rezonanční spektroskopie metody MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
- Názvy látek
- glutamin * MeSH
- kyselina asparagová MeSH
- kyselina glutamová MeSH
Major depressive disorder (MDD) is underlined by neurochemical changes in the brain. Proton magnetic resonance spectroscopy (1H MRS) is a useful tool for their examination as it provides information about the levels of metabolites. This review summarises the current knowledge of 1H MRS findings from rodent models of MDD, assesses the results from both a biological and a technical perspective, and identifies the main sources of bias. From a technical point of view, bias-introducing factors are the diversity of the measured volumes and their positioning in the brain, the data processing, and the metabolite concentration expression. The biological variables are strain, sex, and species, as well as the model itself, and in vivo vs. ex vivo exploration. This review identified some consistency in the 1H MRS findings in the models of MDD: lower levels of glutamine, glutamate + glutamine, and higher levels of myo-inositol and taurine in most of the brain regions of MDD models. This may suggest changes in regional metabolism, neuronal dysregulation, inflammation, and a compensatory effect reaction in the MDD rodent models.
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