Rebecca L Cooper Laboratories, Mental Health Research Institute of Victoria, Parkville, Victoria 3052, Australia.
J Affect Disord. 2012 Feb;136(3):1232-7. doi: 10.1016/j.jad.2011.10.001. Epub 2011 Oct 28.
Glutamate is thought to be involved in the pathophysiology of major depressive disorder and bipolar disorder; however, the molecular changes underlying abnormal glutamatergic signalling remain poorly understood. Whilst previous studies have suggested that the NMDA receptor may be involved in the pathophysiology of mood disorders, it is unclear whether the non-NMDA receptors are also involved. Therefore, we sought to examine whether the expression of the non-NMDA, ionotropic glutamate receptors, AMPA receptor and kainate receptor, is altered in mood disorders.
We used [3H]AMPA and [3H]kainate to measure the levels of AMPA and kainate receptor, respectively, in the anterior cingulate (BA 24) and dorsolateral prefrontal cortex (BA 46) from post-mortem CNS in 10 subjects with major depressive disorder, 10 subjects with bipolar disorder and 10 control subjects.
A 20.7% to 27.7% increase in [3H]AMPA binding density was seen in BA 24 (p<0.05) but not BA 46 (p>0.05) in major depressive disorder compared to control levels. [3H]AMPA binding density was not changed in bipolar disorder in either BA 24 or BA 46 (p>0.05) compared to controls. [3H]Kainate binding was not changed in either BA 24 or BA 46 in either disorder compared to controls (p>0.05).
Small sample sizes (n=10) were used in this study. The subjects were not drug naïve.
Our data suggests increased in AMPA receptor levels in the anterior cingulate are involved in the pathophysiology of major depressive disorder. This data has relevance for the development of new anti-depressant drugs targeted towards the AMPA receptors.
谷氨酸被认为与重性抑郁障碍和双相情感障碍的病理生理学有关;然而,异常谷氨酸能信号转导的分子变化仍知之甚少。虽然先前的研究表明 NMDA 受体可能与心境障碍的病理生理学有关,但尚不清楚非 NMDA 受体是否也参与其中。因此,我们试图研究非 NMDA、离子型谷氨酸受体、AMPA 受体和 kainate 受体的表达是否在心境障碍中发生改变。
我们使用 [3H]AMPA 和 [3H]kainate 分别测量了前扣带回(BA 24)和背外侧前额叶皮层(BA 46)中 AMPA 和 kainate 受体的水平,来自 10 名重性抑郁障碍患者、10 名双相情感障碍患者和 10 名对照者的死后中枢神经系统。
与对照组相比,重性抑郁障碍患者的 BA 24 中 [3H]AMPA 结合密度增加了 20.7%至 27.7%(p<0.05),但 BA 46 中未见增加(p>0.05)。与对照组相比,双相情感障碍患者在 BA 24 或 BA 46 中 [3H]AMPA 结合密度均未改变(p>0.05)。在两种疾病中,[3H]kainate 结合在 BA 24 或 BA 46 中均未改变与对照组相比(p>0.05)。
本研究使用的样本量较小(n=10)。研究对象并非无用药史。
我们的数据表明,前扣带皮层中 AMPA 受体水平的增加与重性抑郁障碍的病理生理学有关。这一数据与开发针对 AMPA 受体的新型抗抑郁药物有关。