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Psychiatric Disorders

studying

  • Education at the D-ITET »»
  • MSc in Biomedical Engineering »»
  • MAS in Medical Physics »»

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This project aims at investigation of the neurobiological basis of different psychiatric disorders and related treatment response. To that clinical symptoms are correlated with metabolic and functional measures obtained in vivo by MRS, functional and structural MRI in humans and animal models.

Metabolites of particular interest are neurotransmitters and their precursors such as glutamine (Gln), glutamate (Glu), and gamma amino butyric acid (GABA), as well as antioxidants such as glutathion (GSH) and ascorbic acid (Asc), whose important roles in the pathophysiology of psychiatric disorders like major depression, schizophrenia, panic disorders or obsessive compulsive disorder are not understood.

In humans these metabolites are currently assessed by JPRESS spectroscopy and 2D prior-knowledge fitting (ProFit) at 3T. In future ultra-high field MRS and MRSI, absolute quantification based on the ERETIC reference standard as well as 13C and 31P MRS might be applied to physiological studies in the context of psychiatric disorders.

From a combined fMRI and MRS study it is hypothesized that severely anhedonic depression is caused by a distortion of the glial reuptake of Glutamate from the synaptic cleft and a downregulation of Glutamate-Glutamine cycling in the pregenual ACC (Walter M, Henning A, Grimm S et al; Arch Gen Psych 66(5), 478-486, 2009)
From a combined fMRI and MRS study it is hypothesized that severely anhedonic depression is caused by a distortion of the glial reuptake of Glutamate from the synaptic cleft and a downregulation of Glutamate-Glutamine cycling in the pregenual ACC (Walter M, Henning A, Grimm S et al; Arch Gen Psych 66(5), 478-486, 2009)

Publications:

Software:

Related MRS projects:

Related MRI projects:

Collaborators:

Contact:

Milan Scheidegger, MD

Anke Henning, PhD

 

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© 2012 ETH Zurich | Imprint | Disclaimer | 18 December 2009
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