Memantine is a N-methyl-D-aspartate (NMDA) receptor antagonist approved for the treatment of moderate to severe Alzheimer's disease (AD). Environmental enrichment (EE) has shown significant beneficial effects on f...Memantine is a N-methyl-D-aspartate (NMDA) receptor antagonist approved for the treatment of moderate to severe Alzheimer's disease (AD). Environmental enrichment (EE) has shown significant beneficial effects on func- tional improvement in AD. In this study, we sought to determine whether combining these two distinct therapies would yield greater benefit than either drug used alone. We investigated the effect of memantine combined with EE on spatial learning and memory and AD-like pathology in a widely used AD model, the senescence-accelerated prone mice (SAMP8). The SAMP8 mice were randomly assigned to enriched housing (EH) or standard housing (SH), where either memantine (20 mg/kg) or saline was given by gastric lavage once daily continuously for eight weeks. Our results showed that, when provided separately, memantine and EE significantly improved spatial learning and memory by shortening escape latencies and increasing the frequency of entrance into the target quadrant. When combined, memantine and EE showed additive effect on learning and memory as evidenced by significant shorter escape latencies and higher frequency of target entrance than either drug alone. Consistent with the behavior results, pathological studies showed that both memantine and EE significantly reduced hippocampal CA1 neurofibrilliary tangles (NFTs) as well as amyloid beta precursor protein (APP) levels. Combining both therapies synergistically lessened NFTs and APP expression compared to either drug alone in SAMP8 mice, indicating that the combination of memantine with EE could offer a novel and efficient therapeutic strategy for the treatment of AD.展开更多
Background:Currently,there is no cure for Alzheimer's disease(AD).Therapeutics that can modify the early stage of AD are urgently needed.Recent studies have shown that the pathogenesis of AD is closely regulated b...Background:Currently,there is no cure for Alzheimer's disease(AD).Therapeutics that can modify the early stage of AD are urgently needed.Recent studies have shown that the pathogenesis of AD is closely regulated by an endo/lysosomal asparaginyl endopeptidase(AEP).Inhibition of AEP has been reported to prevent neural degeneration in transgenic mouse models of AD.However,more than 90% of AD cases are age-related sporadic AD rather than hereditary AD.The therapeutic efficacy of AEP inhibition in ageing-associated sporadic AD remains unknown.Methods:The senescence-accelerated mouse prone 8(SAMP8)was chosen as an approximate model of sporadic AD and treated with a selective AEP inhibitor,δ-secretase inhibitor 11.Activation of AEP was determined by enzymatic activity assay.Concentration of soluble amyloid β(Aβ)in the brain was determined by ELISA.Morris water maze test was performed to assess the learning and memory-related cognitive ability.Pathological changes in the brain were explored by morphological and western blot analyses.Results:The enzymatic activity of AEP in the SAMP8 mouse brain was significantly higher than that in the agematched SAMR1 mice.The half maximal inhibitory concentration(IC_(50))for δ-secretase inhibitor 11 to inhibit AEP in vitro was around 150 nM.Chronic treatment with δ-secretase inhibitor 11 markedly decreased the brain AEP activity,reduced the generation of Aβ_(1-40/42) and ameliorated memory loss.The inhibition of AEP with this reagent not only reduced the AEP-cleaved tau fragments and tau hyperphosphorylation,but also attenuated neuroinflammation in the form of microglial activation.Moreover,treatment with 6-secretase inhibitor 11 prevented the synaptic loss and alleviated dendritic disruption in SAMP8 mouse brain.Conclusions:Pharmacological inhibition of AEP can intervene and prevent AD-like pathological progress in the model of sporadic AD.The up-regulated AEP in the brain could be a promising target for early treatment of AD.The δ-secretase inhibitor 11 can be used as a lead compound for translational development of AD treatment.展开更多
基金supported by a grant from the Natural Sciences Foundation of Jiangsu Province (No. BK2008081)the Scientific Research Fund of Nanjing Medical University (No. 2010NJMU244)
文摘Memantine is a N-methyl-D-aspartate (NMDA) receptor antagonist approved for the treatment of moderate to severe Alzheimer's disease (AD). Environmental enrichment (EE) has shown significant beneficial effects on func- tional improvement in AD. In this study, we sought to determine whether combining these two distinct therapies would yield greater benefit than either drug used alone. We investigated the effect of memantine combined with EE on spatial learning and memory and AD-like pathology in a widely used AD model, the senescence-accelerated prone mice (SAMP8). The SAMP8 mice were randomly assigned to enriched housing (EH) or standard housing (SH), where either memantine (20 mg/kg) or saline was given by gastric lavage once daily continuously for eight weeks. Our results showed that, when provided separately, memantine and EE significantly improved spatial learning and memory by shortening escape latencies and increasing the frequency of entrance into the target quadrant. When combined, memantine and EE showed additive effect on learning and memory as evidenced by significant shorter escape latencies and higher frequency of target entrance than either drug alone. Consistent with the behavior results, pathological studies showed that both memantine and EE significantly reduced hippocampal CA1 neurofibrilliary tangles (NFTs) as well as amyloid beta precursor protein (APP) levels. Combining both therapies synergistically lessened NFTs and APP expression compared to either drug alone in SAMP8 mice, indicating that the combination of memantine with EE could offer a novel and efficient therapeutic strategy for the treatment of AD.
基金supported by the National Natural Science Foundation of China(81671375,91949116 and 81873807)Innovative Research Team of High-level Local Universities in Shanghai,China.
文摘Background:Currently,there is no cure for Alzheimer's disease(AD).Therapeutics that can modify the early stage of AD are urgently needed.Recent studies have shown that the pathogenesis of AD is closely regulated by an endo/lysosomal asparaginyl endopeptidase(AEP).Inhibition of AEP has been reported to prevent neural degeneration in transgenic mouse models of AD.However,more than 90% of AD cases are age-related sporadic AD rather than hereditary AD.The therapeutic efficacy of AEP inhibition in ageing-associated sporadic AD remains unknown.Methods:The senescence-accelerated mouse prone 8(SAMP8)was chosen as an approximate model of sporadic AD and treated with a selective AEP inhibitor,δ-secretase inhibitor 11.Activation of AEP was determined by enzymatic activity assay.Concentration of soluble amyloid β(Aβ)in the brain was determined by ELISA.Morris water maze test was performed to assess the learning and memory-related cognitive ability.Pathological changes in the brain were explored by morphological and western blot analyses.Results:The enzymatic activity of AEP in the SAMP8 mouse brain was significantly higher than that in the agematched SAMR1 mice.The half maximal inhibitory concentration(IC_(50))for δ-secretase inhibitor 11 to inhibit AEP in vitro was around 150 nM.Chronic treatment with δ-secretase inhibitor 11 markedly decreased the brain AEP activity,reduced the generation of Aβ_(1-40/42) and ameliorated memory loss.The inhibition of AEP with this reagent not only reduced the AEP-cleaved tau fragments and tau hyperphosphorylation,but also attenuated neuroinflammation in the form of microglial activation.Moreover,treatment with 6-secretase inhibitor 11 prevented the synaptic loss and alleviated dendritic disruption in SAMP8 mouse brain.Conclusions:Pharmacological inhibition of AEP can intervene and prevent AD-like pathological progress in the model of sporadic AD.The up-regulated AEP in the brain could be a promising target for early treatment of AD.The δ-secretase inhibitor 11 can be used as a lead compound for translational development of AD treatment.