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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >THE COUMARIN SCOPOLETIN POTENTIATES ACETYLCHOLINE RELEASE FROM SYNAPTOSOMES, AMPLIFIES HIPPOCAMPAL LONG-TERM POTENTIATION AND AMELIORATES ANTICHOLINERGIC- AND AGE-IMPAIRED MEMORY
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THE COUMARIN SCOPOLETIN POTENTIATES ACETYLCHOLINE RELEASE FROM SYNAPTOSOMES, AMPLIFIES HIPPOCAMPAL LONG-TERM POTENTIATION AND AMELIORATES ANTICHOLINERGIC- AND AGE-IMPAIRED MEMORY

机译:香豆素水溶素增强了乙酰胆碱从突触体释放,放大海马长期增强,并改善抗胆碱能和年龄损害记忆

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In a previous study the simple, naturally derived coumarin scopoletin (SCT) was identified as an inhibitor of acetylcholinesterase (AChE), using a pharmacophore-based virtual screening approach. In this study the potential of SCT as procholinergic and cognition-enhancing therapeutic was investigated in a more detailed way, using different experimental approaches like measuring newly synthesized acetyl-choline (ACh) in synaptosomes, long-term potentiation (LTP) experiments in hippocampal slices, and behavior studies. SCT enhanced the K~+-stimulated release of ACh from rat frontal cortex synaptosomes, showing a bell-shaped dose effect curve (E_(max): 4 muM). This effect was blocked by the nicotinic ACh receptor (nAChR) antagonists mecamylamine (MEC) and dihydro-beta-erythroidine (DHE). The nAChR agonist (and AChE inhibitor) galantamine induced a similar increase in ACh release (E_(max): 1 muM). SCT potentiated LTP in hippocampal slices of rat brain. The high-frequency stimulation (HFS)-induced, N-methyl-D-aspartate (NMDA) receptor dependent LTP of field excitatory postsynaptic potentials at CA3-CA1 synapses was greatly enhanced by pre-HFS application of SCT (4 muM for 4 min). This effect was mimicked by nicotine (2 muM) and abolished by MEC, suggesting an effect on nAChRs. SCT did not restore the total inhibition of LTP by NMDA receptor antagonist d, L-2-amino-5-phosphonopen-tanoic acid (AP-5). SCT (2 mug, i.c.v.) increased T-maze alternation and ameliorated novel object recognition of mice with scopolamine-induced cholinergic deficit. It also reduced age-associated deficits in object memory of 15-18-month-old mice (2 mg/kg sc). Our findings suggest that SCT possesses memory-improving properties, which are based on its direct nAChR agonistic activity. Therefore, SCT might be able torescue impaired cholinergic functions by enhancing nAChR-mediated release of neurotransmitters and promoting neural plasticity in hippocampus. ? 2011 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:在先前的研究中,使用基于药镜的虚拟筛选方法鉴定为乙酰胆碱酯酶(ACHE)的简单,天然衍生的香豆素Scopoletin(SCT)。在这项研究中,以更详细的方式研究了SCT作为丙基醇能和认知增强治疗的潜力,使用不同的实验方法,如在突触体中测量新合成的乙酰胆碱(ACH),在海马切片中的长期增强(LTP)实验中和行为的研究。 SCT增强了来自大鼠额叶突触突触体的K〜+ +刺激释放,显示出钟形剂量效应曲线(E_(最大):4毫米)。这种效果被尼古洛ACH受体(NACHR)拮抗剂MeCamylamine(MEC)和二氢β-辛辛胺(DHE)阻断。 NACHR激动剂(和ACHE抑制剂)加兰汀在ACH释放(E_(MAX):1妈妈)中诱导类似的增加。 SCT在海马大鼠大脑中具有增强LTP。诱导的高频刺激(HFS)诱导的N-甲基-D-天冬氨酸(NMDA)受体依赖性LTP在CA3-CA1突触处的野外兴奋后突触电位的LTP通过SCT预先应用(4毫米4分钟)。这种效果被尼古丁(2妈妈)模仿,并由MEC废除,表明对NACHRS的影响。 SCT没有恢复NMDA受体拮抗剂D,L-2-氨基-5-膦酸钨酸(AP-5)的LTP的总抑制。 SCT(2杯,I.C.V.)增加了T-Maze交替,并改善了通过CoCopolamine诱导的胆碱能缺陷的小鼠的新型对象识别。它还减少了15-18个月大鼠的物体记忆中的年龄相关的缺陷(2 mg / kg sc)。我们的研究结果表明,SCT具有内存改善的属性,其基于其直接的NACHR激动活动。因此,通过增强NACHR介导的神经递质释放并促进海马的神经可塑性,SCT可能能够受损的胆碱能功能。还是2011年IBRO。 elsevier有限公司出版。保留所有权利。

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