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Background: Major depressive disorder (MDD) is a complex psychiatric illness involving multiple brain regions. Increasing evidence indicates that the striatum is involved in depression, but the molecular mechanisms remain unclear.
Methods: In this study, we performed a gas chromatography-mass spectrometer (GC/MS)-based metabolomic analysis in the striatum of depressed rats induced by chronic unpredictable mild stress (CUMS). We then compared striatal data with our previous data from the hippocampus and cerebellum to systematically investigate the potential pathogenesis of depression.
Results: We identified 22 differential metabolites in the striatum between the CUMS and control groups; these altered metabolites were mainly involved in amino acid, carbohydrate, and nucleotide metabolism. Pathway analysis revealed that the shared metabolic pathways of the striatum, hippocampus, and cerebellum were mainly involved in the glutamine-glutamate metabolic system. Four genes in the striatum (, and ), six genes in the hippocampus (, and ), and five genes in the cerebellum (, and ) were found to be significantly altered using RT-qPCR. Correlation analysis indicated that these differential genes were strongly correlated.
Conclusion: These results suggest that chronic stress might induce depressive behaviors by disturbing the glutamine-glutamate-GABA cycle in the striatum, hippocampus, and cerebellum, and that the glutamine-glutamate-GABA cycle among these three brain regions might generate cooperative action in response to chronic stress.
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http://dx.doi.org/10.2147/NDT.S245282 | DOI Listing |
Mol Biol Rep
September 2025
Department of Pharmacology, Govt. College of Pharmacy, Rohru, Shimla, Himachal Pradesh, 171207, India.
Alzheimer's disease (AD) is the most common, complex, and untreatable form of dementia which is characterized by severe cognitive, motor, neuropsychiatric, and behavioural impairments. These symptoms severely reduce the quality of life for patients and impose a significant burden on caregivers. The existing therapies offer only symptomatic relief without addressing the underlying silent pathological progression.
View Article and Find Full Text PDFJ Neurochem
September 2025
Department of Biology and Biotechnologies "Charles Darwin", Sapienza University of Rome, Rome, Italy.
Patients with Duchenne muscular dystrophy (DMD) may experience neurobehavioral and cognitive concerns, including psychiatric symptoms, due to the absence of full-length dystrophin (Dp427), frequently accompanied by deficiencies in shorter isoforms. The lack of dystrophin affects neurophysiological processes from the uterine phase, impacting neural circuitry in brain regions such as the prefrontal cortex, hippocampus, and cerebellum. This leads to reduced inhibitory GABAergic transmission and altered hippocampal glutamatergic signaling.
View Article and Find Full Text PDFHeterozygous loss-of-function mutations are one established cause of isolated dystonia and hyposmia. Homozygous mutations have been reported in siblings with generalized dystonia and intellectual disability. encodes major [NM_001369387.
View Article and Find Full Text PDFImaging Neurosci (Camb)
September 2025
Physics for Medicine Paris, Inserm, ESPCI Paris-PSL, CNRS, Paris, France.
Functional ultrasound (fUS) is a promising imaging method for evaluating brain function in animals and human neonates. fUS images local cerebral blood volume changes to map brain activity. One application of fUS imaging is the quantification of functional connectivity (FC), which characterizes the strength of the connections between functionally connected brain areas.
View Article and Find Full Text PDFMov Disord Clin Pract
September 2025
Department of Neurology, School of Medical Sciences - University of Campinas (UNICAMP), Campinas, Brazil.
Background: The progression of brain damage in CANVAS/RFC1 remains unclear.
Objective: To describe longitudinal brain changes in CANVAS/RFC1.
Methods: Ten RFC1-positive patients and 10 controls underwent 3T-MRI scans 2 years apart.