Decreased prefrontal glutamatergic function is associated with a reduced astrocyte-related gene expression in treatment-resistant depression

Transl Psychiatry. 2024 Nov 25;14(1):478. doi: 10.1038/s41398-024-03186-2.

Abstract

Glutamatergic dysfunction is involved in the pathophysiology of treatment-resistant depression (TRD). However, few physiological studies have evaluated its pathophysiology in vivo in individuals with TRD. Transcranial magnetic stimulation-electroencephalography (TMS-EEG) techniques can assess intracortical facilitation (ICF), which reflects glutamatergic neurophysiological function in specific cortical regions. The objectives of this study were (1) to compare glutamatergic receptor-mediated function as indexed with ICF TMS-EEG in the dorsolateral prefrontal cortex (DLPFC) between participants with TRD and healthy controls (HCs) and (2) to explore the relationships between cell-specific gene expression levels and the group difference in glutamatergic neural propagation using virtual histology approach. Sixty participants with TRD and thirty HCs were examined with ICF TMS-EEG measure (80 single-pulse TMS and paired-pulse ICF) in the left DLPFC. Both sensor and source-level ICF measures were computed to compare them between the TRD and HC groups. Furthermore, we conducted spatial correlation analyses interregionally between ICF glutamatergic activity and cell-specific gene expression levels employing the Allen Human Brain Atlas dataset. DLPFC-ICF at the sensor level was not significantly different between the two groups, whereas DLPFC-ICF at the source level was reduced in the TRD group compared with the HC group (p = 0.026). Moreover, the reduced ICF signal propagation of TRD correlated with astrocyte-specific gene expression level (p < 0.0001). The glutamatergic neural activities indexed by ICF in the left DLPFC were decreased in participants with TRD. Additionally, a relative reduction in glutamatergic signal propagation originating from the DLPFC in TRD may be associated with astrocytic abnormality.

MeSH terms

  • Adult
  • Astrocytes* / metabolism
  • Case-Control Studies
  • Depressive Disorder, Treatment-Resistant* / genetics
  • Depressive Disorder, Treatment-Resistant* / physiopathology
  • Depressive Disorder, Treatment-Resistant* / therapy
  • Dorsolateral Prefrontal Cortex*
  • Electroencephalography*
  • Female
  • Gene Expression* / genetics
  • Glutamic Acid* / metabolism
  • Humans
  • Male
  • Middle Aged
  • Prefrontal Cortex / metabolism
  • Prefrontal Cortex / physiopathology
  • Transcranial Magnetic Stimulation*

Substances

  • Glutamic Acid