AI Article Synopsis
- Glutathione (GSH) is vital for brain health, and this study aimed to measure its levels in people with major depressive disorder (MDD) and obsessive-compulsive disorder (OCD) compared to healthy controls using advanced imaging techniques.* -
- Results showed that GSH levels were significantly lower in both patient groups, and while healthy individuals had positive correlations between GSH and glutamate levels, these correlations were absent in the MDD and OCD groups.* -
- The findings indicate that lower GSH levels may contribute to oxidative stress and disrupted neurotransmitter signaling, potentially enhancing our understanding of the neurobiological underpinnings of MDD and OCD.*
Article Abstract
Background: Glutathione (GSH) is a crucial antioxidant in the human brain. Although proton magnetic resonance spectroscopy using the Mescher-Garwood point-resolved spectroscopy sequence is highly recommended, limited literature has measured cortical GSH using this method in major psychiatric disorders.
Methods: By combining magnetic resonance spectroscopy and resting-state functional magnetic resonance imaging, we quantified brain GSH and glutamate in the medial prefrontal cortex and precuneus and explored relationships between GSH levels and intrinsic neuronal activity as well as clinical symptoms among healthy control (HC) participants (n = 30), people with major depressive disorder (MDD) (n = 28), and people with obsessive-compulsive disorder (OCD) (n = 28).
Results: GSH concentrations were lower in the medial prefrontal cortex and precuneus in both the MDD and OCD groups than in the HC group. In the HC group, positive correlations were noted between GSH and glutamate levels and between GSH and fractional amplitude of low-frequency fluctuations in both regions. However, while these correlations were absent in both patient groups, there was a weak positive correlation between glutamate and fractional amplitude of low-frequency fluctuations. Moreover, GSH levels were negatively correlated with depressive and compulsive symptoms in MDD and OCD, respectively.
Conclusions: These findings suggest that reduced GSH levels and an imbalance between GSH and glutamate could increase oxidative stress and alter neurotransmitter signaling, thereby leading to disruptions in GSH-related neurochemical-neuronal coupling and psychopathologies across MDD and OCD. Understanding these mechanisms could provide valuable insights into the processes that underlie these disorders and potentially become a springboard for future directions and advancing our knowledge of their neurobiological foundations.
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| http://dx.doi.org/10.1016/j.biopsych.2024.08.018 | DOI Listing |
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