Peters Marco, Bletsch Matthew, Stanley Jennifer, Wheeler Damian, Scott Roderick, Tully Tim
Dart Neuroscience, LLC, San Diego, CA, USA.
Neuropsychopharmacology. 2014 Dec;39(13):2938-48. doi: 10.1038/npp.2014.154. Epub 2014 Jun 26.
Aging is associated with declines in memory and cognitive function. Here, we evaluate the effects of HT-0712 on memory formation and on cAMP response element-binding protein (CREB)-regulated genes in aged mice. HT-0712 enhanced long-term memory formation in normal young mice at brain concentrations similar to those found to increase CRE-mediated gene expression in hippocampal neurons. Aged mice showed significantly poorer contextual and trace conditioning compared with young-adult mice. In aged mice, a single injection of HT-0712 significantly boosted contextual and trace long-term memory. Additional effects of HT-0712 were seen in a spatial memory task. Our parallel biochemical experiments revealed that inductions of the CREB-regulated genes, cFos, Zif268, and Bdnf, after fear conditioning were diminished in aged mice. HT-0712 facilitated expression of these CREB-regulated genes in aged hippocampus, indicating that the drug engages a CREB-regulated mechanism in vivo. These findings corroborate and extend our previous results on the mechanism of action of HT-0712 and its efficacy to enhance memory formation. Our data also indicate that HT-0712 may be effective to treat age-associated memory impairment in humans.
衰老与记忆力和认知功能的衰退有关。在此,我们评估了HT-0712对老年小鼠记忆形成及环磷腺苷反应元件结合蛋白(CREB)调控基因的影响。在大脑中的浓度与在海马神经元中发现的增加CRE介导的基因表达的浓度相似时,HT-0712增强了正常年轻小鼠的长期记忆形成。与年轻成年小鼠相比,老年小鼠的情境性和痕迹性条件反射明显较差。在老年小鼠中,单次注射HT-0712显著增强了情境性和痕迹性长期记忆。在空间记忆任务中也观察到了HT-0712的其他作用。我们的平行生化实验表明,在恐惧条件反射后,老年小鼠中CREB调控基因cFos、Zif268和Bdnf的诱导作用减弱。HT-0712促进了老年海马体中这些CREB调控基因的表达,表明该药物在体内参与了一种由CREB调控的机制。这些发现证实并扩展了我们之前关于HT-0712作用机制及其增强记忆形成功效的研究结果。我们的数据还表明,HT-0712可能对治疗人类与年龄相关的记忆障碍有效。