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Effect of galantamine on the human α7 neuronal nicotinic acetylcholine receptor the Torpedo nicotinic acetylcholine receptor and spontaneous cholinergic synaptic activity

机译:加兰他敏对人α7神经元烟碱乙酰胆碱受体鱼雷烟碱乙酰胆碱受体和自发胆碱能突触活性的影响

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摘要

class="enumerated" style="list-style-type:decimal">Various types of anticholinesterasic agents have been used to improve the daily activities of Alzheimer's disease patients. It was recently demonstrated that Galantamine, described as a molecule with anticholinesterasic properties, is also an allosteric enhancer of human α4β2 neuronal nicotinic receptor activity. We explored its effect on the human α7 neuronal nicotinic acetylcholine receptor (nAChR) expressed in Xenopus oocytes.Galantamine, at a concentration of 0.1 μM, increased the amplitude of acetylcholine (ACh)-induced ion currents in the human α7 nAChR expressed in Xenopus oocytes, but caused inhibition at higher concentrations. The maximum effect of galantamine, an increase of 22% in the amplitude of ACh-induced currents, was observed at a concentration of 250 μM Ach.The same enhancing effect was obtained in oocytes transplanted with Torpedo nicotinic acetylcholine receptor (AChR) isolated from the electric organ, but in this case the optimal concentration of galantamine was 1 μM. In this case, the maximum effect of galantamine, an increase of 35% in the amplitude of ACh-induced currents, occurred at a concentration of 50 μM ACh.Galantamine affects not only the activity of post-synaptic receptors but also the activity of nerve terminals. At a concentration of 1 μM, quantal spontaneous events, recorded in a cholinergic synapse, increased their amplitude, an effect which was independent of the anticholinesterasic activity associated with this compound. The anticholinesterasic effect was recorded in preparations treated with a galantamine concentration of 10 μM.In conclusion, our results show that galantamine enhances human α7 neuronal nicotinic ACh receptor activity. It also enhances muscular AChRs and the size of spontaneous cholinergic synaptic events. However, only a very narrow range of galantamine concentrations can be used for enhancing effects.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 各种类型的抗胆碱药已被用于改善阿尔茨海默氏病患者的日常活动。最近证实,被描述为具有抗胆碱能特性的分子的加兰他敏也是人α4β2神经元烟碱样受体活性的变构增强剂。我们探讨了其对非洲爪蟾卵母细胞中表达的人α7神经元烟碱乙酰胆碱受体(nAChR)的作用。 加兰他敏,浓度为0.1μμM,增加了乙酰胆碱(ACh)诱导的离子电流幅度。人α7nAChR在非洲爪蟾卵母细胞中表达,但在较高浓度下引起抑制。在浓度为250μMAch的情况下,观察到加兰他敏的最大作用,即使ACh诱导的电流幅度增加22%。 在鱼雷烟碱型乙酰胆碱移植的卵母细胞中获得了相同的增强作用。从电子器官中分离出的受体(AChR),但在这种情况下,加兰他敏的最佳浓度为1μM。在这种情况下,加兰他敏的最大作用是在50μMACh的浓度下使ACh诱导的电流幅度增加35%。 加兰他敏不仅影响突触后的活动受体,还有神经末梢的活性。在浓度为1μM的情况下,以胆碱能突触记录的数量性自发事件增加了其振幅,该效应独立于与该化合物相关的抗胆碱酯酶活性。在加兰他敏浓度为10μm的制剂中记录了其抗胆碱能的作用。 总而言之,我们的结果表明,加兰他敏可增强人α7神经元烟碱型ACh受体的活性。它还增强了肌肉AChRs和自发性胆碱能突触事件的大小。但是,只有很小范围的加兰他敏浓度可以用于增强效果。

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