Yu Ling, An Shu-Cheng, Lian Ting
College of Life Science, Shaanxi Normal University, Xi'an 710062, China.
Sheng Li Xue Bao. 2010 Feb 25;62(1):14-22.
The present study was aimed to investigate the role and relationship between N-methyl-D-aspartic acid (NMDA) receptor and neuropeptide Y (NPY) in depression induced by chronic unpredictable mild stress (CUMS). CUMS-induced depression model was established in Sprague-Dawley rats. Intrahippocampal injections of NMDA, non-competitive NMDA receptor antagonist MK-801 and NPY-Y1 receptor antagonist GR231118 were respectively adopted by rat brain stereotaxic coordinates. The behavioral observations were conducted by sucrose consumption test, open field test and forced swimming test. The expression of NPY in hippocampus was detected by immunohistochemistry. The results showed that compared with the control group, rats receiving CUMS for 21 days or intrahippocampal injection of GR231118 or NMDA showed depression-like behavioral changes, including a reduction in sucrose preference, body weight, locomotor activity, rearing and grooming in open field test, and increased duration of immobility in forced swimming test. Intrahippocampal injection of NMDA decreased the expression of NPY in hippocampal CA3 region and dentate gyrus (DG) region. Intrahippocampal injection of MK-801 improved the depression-like behavioral changes induced by CUMS, and increased the expression of NPY in hippocampal CA3 region and DG region. Co-injection of GR231118 and MK-801showed that GR231118 suppressed the antidepressant effect of MK-801. These data suggest that CUMS might induce depression through excessive release of glutamate (Glu), over-activation of NMDA receptors, and downregulation of NPY. Antidepressant effect of NPY was mainly mediated via NPY-Y1 receptor.
本研究旨在探讨N-甲基-D-天冬氨酸(NMDA)受体与神经肽Y(NPY)在慢性不可预测温和应激(CUMS)诱导的抑郁症中的作用及关系。在Sprague-Dawley大鼠中建立CUMS诱导的抑郁症模型。采用大鼠脑立体定位坐标分别进行海马内注射NMDA、非竞争性NMDA受体拮抗剂MK-801和NPY-Y1受体拮抗剂GR231118。通过蔗糖消耗试验、旷场试验和强迫游泳试验进行行为观察。采用免疫组织化学法检测海马中NPY的表达。结果显示,与对照组相比,接受21天CUMS或海马内注射GR231118或NMDA的大鼠表现出抑郁样行为变化,包括蔗糖偏好降低、体重减轻、旷场试验中的运动活动、竖毛和理毛行为减少,以及强迫游泳试验中不动时间增加。海马内注射NMDA可降低海马CA3区和齿状回(DG)区NPY的表达。海马内注射MK-801可改善CUMS诱导的抑郁样行为变化,并增加海马CA3区和DG区NPY的表达。GR231118和MK-801共同注射显示,GR231118可抑制MK-801的抗抑郁作用。这些数据表明,CUMS可能通过谷氨酸(Glu)过度释放、NMDA受体过度激活和NPY下调诱导抑郁症。NPY的抗抑郁作用主要通过NPY-Y1受体介导。