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白藜芦醇和反式-ε-葡萄素对非洲爪蟾卵母细胞中表达的GABAA受体亚型上GABA诱导电流的差异作用。

The Differential Effects of Resveratrol and trans-ε-Viniferin on the GABA-Induced Current in GABAA Receptor Subtypes Expressed in Xenopus Laevis Oocytes.

作者信息

Groundwater Paul William, Hamid Kaiser, Ng Irene, Tallapragada Vikram J, Hibbs David E, Hanrahan Jane

机构信息

Faculty of Pharmacy University of Sydney.

出版信息

J Pharm Pharm Sci. 2015;18(4):328-38. doi: 10.18433/j3qw3k.

Abstract

PURPOSE

The natural products resveratrol and trans-ε-viniferin have been reported to have many beneficial effects, which include the enhancement of cognition and memory. There have been no studies which have reported the effects of these compounds on the different GABAA receptor subtypes and this study aimed to address this.

METHODS

The effects of both resveratrol, and its dimer, trans-ε-viniferin, have been investigated on different GABAA receptor subtypes expressed in Xenopus laevis oocytes, using the two-electrode voltage clamp technique.

RESULTS

Resveratrol induced a current of 22 ± 3.53 nA in the α1β2γ2L subtype of the GABAA receptor (but not in the α5β3γ2L and α2β2γ2L subtypes) when applied alone. It also positively modulated the GABA-induced current (IGABA) in α1β2γ2L receptors, in adose-dependent manner (EC50 58.24 μM). The effects of resveratrol were not sensitive to the benzodiazepine antagonist flumazenil. trans-ε-Viniferin exhibited a different pattern of activity to resveratrol; it alone had no effect on any of the subtypes, but it did negatively modulate the GABA-induced current (IGABA) in all three subtypes. The greatest inhibition was found in the α1β2γ2L subtype (IC50 5.79 μM), with the inhibition in the α2β2γ2L (IC50 of 19.08 μM) and α5β3γ2L (IC50 of 21.05 μM) subtypes being similar. The effects of trans-ε-viniferin in α1β2γ2L and α2β2γ2L receptors werealso not sensitive to the benzodiazepine antagonist flumazenil while, in the α5β3γ2L subtype the effect was not sensitive to the inverse agonist L-655,708, indicating different binding sites for this molecule.

CONCLUSIONS

The results of the present study indicate that both resveratrol and trans-ε-viniferin modulate the GABA-induced current in different ways, and that trans-ε-viniferin may be a lead compound for the discovery of agents which selectively inhibit the GABA-induced current in α1-containing subtypes.This article is open to POST-PUBLICATION REVIEW. Registered readers (see "For Readers") may comment by clicking on ABSTRACT on the issue's contents page.

摘要

目的

据报道,天然产物白藜芦醇和反式-ε-葡萄素具有多种有益作用,包括增强认知和记忆。尚未有研究报道这些化合物对不同GABAA受体亚型的影响,本研究旨在解决这一问题。

方法

采用双电极电压钳技术,研究了白藜芦醇及其二聚体反式-ε-葡萄素对非洲爪蟾卵母细胞中表达的不同GABAA受体亚型的影响。

结果

单独应用白藜芦醇时,可在GABAA受体的α1β2γ2L亚型中诱导出22±3.53 nA的电流(但在α5β3γ2L和α2β2γ2L亚型中未诱导出电流)。它还以剂量依赖的方式(EC50为58.24 μM)正向调节α1β2γ2L受体中GABA诱导的电流(IGABA)。白藜芦醇的作用对苯二氮䓬拮抗剂氟马西尼不敏感。反式-ε-葡萄素表现出与白藜芦醇不同的活性模式;它单独对任何亚型均无作用,但它确实对所有三种亚型中的GABA诱导电流(IGABA)产生负向调节作用。在α1β2γ2L亚型中发现的抑制作用最大(IC50为5.79 μM),α2β2γ2L(IC50为19.08 μM)和α5β3γ2L(IC50为21.05 μM)亚型中的抑制作用相似。反式-ε-葡萄素在α1β2γ2L和α2β2γ2L受体中的作用对苯二氮䓬拮抗剂氟马西尼也不敏感,而在α5β3γ2L亚型中,其作用对反向激动剂L-655,708不敏感,表明该分子具有不同的结合位点。

结论

本研究结果表明,白藜芦醇和反式-ε-葡萄素均以不同方式调节GABA诱导的电流,并且反式-ε-葡萄素可能是发现选择性抑制含α1亚型中GABA诱导电流的药物的先导化合物。本文接受发表后审查。注册读者(见“给读者的信息”)可通过点击本期目录页上的摘要进行评论。

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