Chen Hu, Pandey Ghanshyam N, Dwivedi Yogesh
Department of Psychiatry, Psychiatric Institute, University of Illinois at Chicago, Chicago, Illinois 60612, USA.
Neuroreport. 2006 Jun 26;17(9):863-7. doi: 10.1097/01.wnr.0000221827.03222.70.
A recent hypothesis suggests reduced hippocampal neurogenesis in depression. Here, we examined cell proliferation in the dentate gyrus and the subventricular zone of rats given repeated stress, a paradigm that prolongs learned helplessness behavior, and whether antidepressants modulate the learned helplessness-associated altered cell proliferation. Decreased cell proliferation, number of clusters, and cells/cluster were noted in the dentate gyrus, but not in the subventricular zone, of learned helplessness rats. Both fluoxetine and desipramine reversed the learned helplessness behavior and increased the cell proliferation and the number of clusters in learned helplessness rats; only fluoxetine did so significantly. Both fluoxetine and desipramine significantly increased the number of cells/cluster. Our results suggest modified hippocampal neurogenesis in prolonged depression and in the mechanism of antidepressant action.
最近有假说认为抑郁症患者海马体神经发生减少。在此,我们检测了遭受反复应激的大鼠齿状回和脑室下区的细胞增殖情况,反复应激是一种会延长习得性无助行为的范式,同时还研究了抗抑郁药是否能调节与习得性无助相关的细胞增殖改变。我们发现,习得性无助大鼠的齿状回中细胞增殖、细胞簇数量及每个细胞簇中的细胞数量均减少,但脑室下区未出现此现象。氟西汀和地昔帕明均可逆转习得性无助行为,并增加习得性无助大鼠的细胞增殖及细胞簇数量;只有氟西汀的作用具有显著性。氟西汀和地昔帕明均显著增加了每个细胞簇中的细胞数量。我们的研究结果提示,在长期抑郁症及抗抑郁药作用机制中,海马体神经发生存在改变。