Brain metabolic derangements examined using 1H MRS and their (in)consistency among different rodent models of depression
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Review, Research Support, Non-U.S. Gov't
PubMed
37301420
DOI
10.1016/j.pnpbp.2023.110808
PII: S0278-5846(23)00094-5
Knihovny.cz E-resources
- Keywords
- Animal models, Depression, Metabolites, Proton magnetic resonance spectroscopy,
- MeSH
- Depression MeSH
- Depressive Disorder, Major * metabolism MeSH
- Glutamine * metabolism MeSH
- Rodentia metabolism MeSH
- Aspartic Acid metabolism MeSH
- Glutamic Acid metabolism MeSH
- Brain metabolism MeSH
- Proton Magnetic Resonance Spectroscopy methods MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Glutamine * MeSH
- Aspartic Acid MeSH
- Glutamic Acid 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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