Jitang College of Hebei United University, Tangshan 063000, People's Republic of China.
Neurochem Res. 2013 Jan;38(1):98-107. doi: 10.1007/s11064-012-0894-y. Epub 2012 Sep 26.
Curcumin has neuroprotective effect and could enhance memory. However, the mechanisms underlying the protection of curcumin on aging-related memory decline are not well understood. In this study, high frequency stimulation (HFS)-induced long term potentiation (LTP) was evaluated by a cellular model of memory formation. A two-input stimulation paradigm was used to record the potentiation as well as synapse input specificity. The data suggested that an N-Methyl-D-aspartate receptors (NMDAR) -dependent LTP was inducible in adult hippocampal slices with a characteristic of synapse input specificity. It also indicated that aging resulted in a reduction in LTP but more importantly a loss of synaptic input specificity. The reason behind the above conclusions is that LTP induction is more dependent on the calcium channel. This is due to a switch of the dependence of LTP induction to voltage-dependent calcium channel (VDCC) compared to NMDA receptors. Curcumin administration recovers input specificity by re-establishing NMDA receptor dependence of induction. In addition, curcumin administration ameliorated aging-related increase of brain thiobarbituric acid-reactive substances and elevated aging-related decrease of glutathione in hippocampus. It is then concluded that curcumin modulates hippocampal redox status and restores aging-related loss of synapse input specificity of HFS-induced LTP by switching VDCC calcium source into NMDA receptor-dependent one.
姜黄素具有神经保护作用,可增强记忆。然而,姜黄素对与衰老相关的记忆减退的保护机制尚不清楚。在这项研究中,通过记忆形成的细胞模型评估了高频刺激(HFS)诱导的长期增强(LTP)。使用双输入刺激范式记录增强以及突触输入特异性。数据表明,在成年海马切片中可以诱导 N-甲基-D-天冬氨酸受体(NMDAR)依赖性 LTP,具有突触输入特异性的特征。它还表明,衰老导致 LTP 减少,但更重要的是丧失了突触输入特异性。上述结论的原因是 LTP 诱导更依赖于钙通道。这是由于与 NMDA 受体相比,LTP 诱导对电压依赖性钙通道(VDCC)的依赖性发生了转变。姜黄素通过重新建立诱导的 NMDA 受体依赖性来恢复输入特异性。此外,姜黄素的给药通过将 VDCC 钙源切换到 NMDA 受体依赖性来改善与衰老相关的脑硫代巴比妥酸反应物质的增加和海马中与衰老相关的谷胱甘肽减少。因此,姜黄素通过将 VDCC 钙源切换到 NMDA 受体依赖性,调节海马的氧化还原状态,并恢复与衰老相关的 HFS 诱导的 LTP 的突触输入特异性丧失。