Lee Sang Won, Kim Seungho, Chang Yongmin, Cha Hyunsil, Noeske Ralph, Choi Changho, Lee Seung Jae
Department of Psychiatry, School of Medicine, Kyungpook National University, Daegu, Korea; Department of Psychiatry, Kyungpook National University Chilgok Hospital, Daegu, Korea.
Department of Medical & Biological Engineering, Kyungpook National University, Daegu, Korea.
Biol Psychiatry. 2025 Feb 1;97(3):279-289. doi: 10.1016/j.biopsych.2024.08.018. Epub 2024 Aug 30.
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.
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).
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.
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.
谷胱甘肽(GSH)是人类大脑中一种关键的抗氧化剂。尽管强烈推荐使用Mescher-Garwood点分辨波谱序列进行质子磁共振波谱分析,但在主要精神疾病中,使用这种方法测量皮质GSH的文献有限。
通过结合磁共振波谱分析和静息态功能磁共振成像,我们对健康对照(HC)参与者(n = 30)、重度抑郁症(MDD)患者(n = 28)和强迫症(OCD)患者(n = 28)的内侧前额叶皮质和楔前叶中的脑GSH和谷氨酸进行了定量,并探讨了GSH水平与内在神经元活动以及临床症状之间的关系。
MDD组和OCD组的内侧前额叶皮质和楔前叶中的GSH浓度均低于HC组。在HC组中,两个区域内GSH与谷氨酸水平之间以及GSH与低频波动分数振幅之间均呈正相关。然而,在两个患者组中均未发现这些相关性,而谷氨酸与低频波动分数振幅之间存在微弱的正相关。此外,GSH水平分别与MDD和OCD中的抑郁和强迫症状呈负相关。
这些发现表明,GSH水平降低以及GSH与谷氨酸之间的失衡可能会增加氧化应激并改变神经递质信号传导,从而导致MDD和OCD中与GSH相关的神经化学-神经元耦合和精神病理学的破坏。了解这些机制可为这些疾病的潜在过程提供有价值的见解,并有可能成为未来研究方向的跳板,增进我们对其神经生物学基础的认识。