Department of Pathophysiology, School of Medicine, Wuhan University of Science and Technology, Wuhan, Hubei, China.
J Neurochem. 2012 Aug;122(4):800-11. doi: 10.1111/j.1471-4159.2012.07830.x. Epub 2012 Jul 9.
7,8-dihydroxyflavone (7,8-DHF) has recently been identified as a potential TrkB agonist that crosses the blood-brain barrier after i.p. administration. We previously demonstrated that 7,8-DHF in vitro rescues long-term synaptic plasticity in the hippocampus of aged rats. This study assessed the rescue effect of 7,8-DHF in vivo on aging-related cognitive impairment in rats, and further determined whether the effect of 7,8-DHF is age dependent. Aged rats at 22 and 30 months of age were pretested for spatial memory in Morris water maze. The aged-impaired rats were retested twice during 7,8-DHF or vehicle treatment, which started 3 weeks after the completion of the pretest. In the 22-month-old rats, daily i.p. administration of 7,8-DHF for 2 weeks improved spatial memory. The improvement in behavioral tests was associated with increases in synapse formation and facilitation of synaptic plasticity in the hippocampus, as well as the activation of several proteins crucial to synaptic plasticity and memory. A more extended treatment paradigm with 7,8-DHF was required to achieve a significant memory improvement in the severely impaired 30-month-old rats. Moreover, 7,8-DHF moderately facilitated the synaptic plasticity, modified the density but not number of spines in the hippocampus of the oldest rats. Taken together, our results suggest that 7,8-DHF can act in vivo to counteract aging-induced declines in spatial memory and synaptic plasticity and morphological changes of hippocampal neurons. The effect of 7,8-DHF is more pronounced in relatively younger impaired rats than in those of more advanced age. These findings demonstrate the reversal of age-dependent memory impairment by in vivo 7,8-DHF application and support the benefit of early treatment for cognitive aging.
7,8-二羟基黄酮(7,8-DHF)最近被鉴定为一种潜在的 TrkB 激动剂,可在腹腔注射后穿过血脑屏障。我们之前证明,7,8-DHF 在体外可挽救老年大鼠海马体的长期突触可塑性。本研究评估了 7,8-DHF 在体内对大鼠与年龄相关的认知障碍的挽救作用,并进一步确定了 7,8-DHF 的作用是否与年龄有关。22 个月和 30 个月大的老年大鼠在 Morris 水迷宫中进行空间记忆的预测试。在 7,8-DHF 或载体治疗开始后 3 周,对老年受损大鼠进行了两次重新测试。在 22 个月大的大鼠中,7,8-DHF 的每日腹腔注射治疗 2 周可改善空间记忆。行为测试的改善与海马体中突触形成的增加和突触可塑性的促进有关,以及对突触可塑性和记忆至关重要的几种蛋白质的激活有关。在严重受损的 30 个月大的大鼠中,需要更延长的 7,8-DHF 治疗方案才能实现显著的记忆改善。此外,7,8-DHF 适度促进了突触可塑性,改变了海马体中棘突的密度但不改变数量。总的来说,我们的研究结果表明,7,8-DHF 可以在体内发挥作用,抵抗与年龄相关的空间记忆和突触可塑性下降以及海马体神经元形态变化。7,8-DHF 的作用在相对年轻的受损大鼠中比在年龄较大的大鼠中更为明显。这些发现表明,通过体内应用 7,8-DHF 可以逆转与年龄相关的记忆障碍,并支持对认知衰老进行早期治疗的益处。