Department of Psychiatry, University of British Columbia, Vancouver, BC, Canada.
Int J Neuropsychopharmacol. 2011 Sep;14(8):1069-74. doi: 10.1017/S1461145711000617. Epub 2011 May 9.
Antioxidant defence systems have received increasing attention in the pathophysiology of psychiatric disorders, including: bipolar disorder (BD), major depressive disorder (MDD), and schizophrenia (SCZ). Recently, we reported decreased glutathione (GSH) levels in post-mortem prefrontal cortex from patients with BD, MDD, and SCZ. To explore this further, we evaluated the levels of two glutathione S-transferase (GST) isoforms via immunoblotting: GST Pi and GST Mu. GST Pi levels were not affected in any of the patients groups vs. controls. GST Mu levels were significantly decreased in patients with MDD and SCZ but not BD. Compared to controls, GST Mu levels were not different in BD patients who had been treated with mood stabilizers at the time of death but were significantly lower in those not taking mood stabilizers at the time of death. These data suggest that GST Mu may be a target for mood stabilizers.
抗氧化防御系统在精神疾病的病理生理学中受到越来越多的关注,包括:双相情感障碍(BD)、重度抑郁症(MDD)和精神分裂症(SCZ)。最近,我们报道了 BD、MDD 和 SCZ 患者死后前额叶皮层的谷胱甘肽(GSH)水平降低。为了进一步探讨这一问题,我们通过免疫印迹法评估了两种谷胱甘肽 S-转移酶(GST)同工酶的水平:GST Pi 和 GST Mu。GST Pi 水平在任何患者组与对照组之间均无差异。MDD 和 SCZ 患者的 GST Mu 水平显著降低,但 BD 患者则没有。与对照组相比,在死亡时正在服用情绪稳定剂的 BD 患者中,GST Mu 水平没有差异,但在死亡时未服用情绪稳定剂的患者中,GST Mu 水平显著降低。这些数据表明,GST Mu 可能是情绪稳定剂的作用靶点。