Bettio Luis E B, Gil-Mohapel Joana, Patten Anna R, O'Rourke Natasha F, Hanley Ronan P, Gopalakrishnan Karthik, Wulff Jeremy E, Christie Brian R
Division of Medical Sciences and UBC Island Medical Program, University of Victoria, Victoria, British Columbia, Canada.
Department of Chemistry, University of Victoria, Victoria, British Columbia, Canada.
Neurogenesis (Austin). 2017 Jun 1;4(1):e1317692. doi: 10.1080/23262133.2017.1317692. eCollection 2017.
The development of synthetic small molecules capable of promoting neuronal fate in stem cells is a promising strategy to prevent the decline of hippocampal function caused by several neurological disorders. Within this context, isoxazole 9 (Isx-9) has been shown to strongly induce cell proliferation and neuronal differentiation in the subgranular zone (SGZ) of the hippocampal dentate gyrus (DG), while also improving hippocampal function in healthy mice. We have recently demonstrated that Isx-9 is able to restore normal neurogenesis levels after procedural stress. Here, we further discuss these findings highlighting the importance of including a naïve group in studies investigating the effects of either restraint stress or mild chronic unpredictable stress (CUS) on adult hippocampal neurogenesis.
开发能够促进干细胞向神经元命运转变的合成小分子,是预防多种神经疾病导致海马体功能衰退的一种有前景的策略。在此背景下,异恶唑9(Isx-9)已被证明能强烈诱导海马齿状回(DG)颗粒下区(SGZ)的细胞增殖和神经元分化,同时还能改善健康小鼠的海马体功能。我们最近证明,Isx-9能够在程序性应激后恢复正常的神经发生水平。在这里,我们进一步讨论这些发现,强调在研究束缚应激或轻度慢性不可预测应激(CUS)对成年海马体神经发生的影响时纳入未受处理组的重要性。