Section on Neuroplasticity, National Institute of Mental Health, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland.
Section on Neuroplasticity, National Institute of Mental Health, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland.
Biol Psychiatry. 2017 Dec 15;82(12):914-923. doi: 10.1016/j.biopsych.2017.05.013. Epub 2017 May 22.
Hippocampal volume loss is a hallmark of clinical depression. Chronic stress produces volume loss in the hippocampus in humans and atrophy of CA3 pyramidal cells and suppression of adult neurogenesis in rodents.
To investigate the relationship between decreased adult neurogenesis and stress-induced changes in hippocampal structure and volume, we compared the effects of chronic unpredictable restraint stress and inhibition of neurogenesis in a rat pharmacogenetic model.
Chronic unpredictable restraint stress over 4 weeks decreased total hippocampal volume, reflecting loss of volume in all hippocampal subfields and in both dorsal and ventral hippocampus. In contrast, complete inhibition of adult neurogenesis for 4 weeks led to volume reduction only in the dentate gyrus. With prolonged inhibition of neurogenesis for 8 or 16 weeks, volume loss spread to the CA3 region, but not CA1. Combining stress and inhibition of adult neurogenesis did not have additive effects on the magnitude of volume loss but did produce a volume reduction throughout the hippocampus. One month of chronic unpredictable restraint stress and inhibition of adult neurogenesis led to atrophy of pyramidal cell apical dendrites in dorsal CA3 and to neuronal reorganization in ventral CA3. Stress also significantly affected granule cell dendrites.
The findings suggest that adult neurogenesis is required to maintain hippocampal volume but is not responsible for stress-induced volume loss.
海马体体积的损失是临床抑郁症的一个标志。慢性应激会导致人类海马体体积减小,以及啮齿动物 CA3 锥体神经元萎缩和成年神经发生受到抑制。
为了研究成年神经发生减少与应激诱导的海马结构和体积变化之间的关系,我们比较了慢性不可预测的束缚应激和在大鼠药物遗传学模型中抑制神经发生的作用。
4 周的慢性不可预测的束缚应激导致总海马体体积减少,反映了所有海马体亚区以及背侧和腹侧海马体的体积损失。相比之下,4 周完全抑制成年神经发生仅导致齿状回体积减少。随着神经发生抑制持续 8 或 16 周,体积损失扩散到 CA3 区,但不包括 CA1 区。将应激和成年神经发生抑制相结合对体积损失的幅度没有相加作用,但确实导致整个海马体的体积减少。1 个月的慢性不可预测的束缚应激和成年神经发生抑制导致背侧 CA3 锥体神经元的树突萎缩,并导致腹侧 CA3 中的神经元重组。应激也显著影响颗粒细胞树突。
这些发现表明,成年神经发生对于维持海马体体积是必需的,但不是应激诱导的体积损失的原因。