首页> 外文期刊>European Journal of Pharmacology: An International Journal >Monoterpene ??-thujone exerts a differential inhibitory action on GABAA receptors implicated in phasic and tonic GABAergic inhibition
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Monoterpene ??-thujone exerts a differential inhibitory action on GABAA receptors implicated in phasic and tonic GABAergic inhibition

机译:单萜ε-丁酮对GABAA受体具有不同的抑制作用,该GABAA受体与阶段性和强直性GABA抑制有关

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摘要

A monoterpene ketone, ??-thujone originally attracted attention as a major natural ingredient of absinthe and was suspected to cause adverse effects such as hallucinations and seizures in persons excessively consuming this beverage. Although subsequent studies ruled out any major role of ??-thujone in the absynthism, it was found that at high doses it may induce epileptic activity pointing to an interaction with GABAergic inhibition. Indeed, subsequent studies, including those from this laboratory, showed that ??-thujone inhibits GABAergic currents. However, GABAA receptors are extremely heterogeneous and in the present study we have investigated the effect of ??-thujone on different recombinant GABAA receptors (??1??2??2L, ?? 1??2, ??1??2?? and ??4??2??) relevant to phasic or tonic forms of inhibition. We report that ??-thujone inhibits all considered receptor types by a qualitatively similar mechanism but the strongest effect is observed for ??1??2?? receptors, suggesting that tonic currents might be more sensitive to ??-thujone than the phasic ones. Moreover, we demonstrate that tonic currents, mimicked by response to a submicromollar GABA concentration (0.3 ??M) in cultured neurons, showed a substantially larger sensitivity to ??-thujone than responses elicited by higher [GABA] (more similar to phasic currents) or Inhibitory Postsynaptic Currents in the same preparation. Importantly, the extent of tonic current inhibition by ??-thujone was as strong as in the case of currents mediated by ??1??2?? receptors. Altogether, these data provide evidence that different GABAA receptor subtypes show distinct sensitivities to ??-thujone and suggest that this compound may differentially affect tonic and phasic components of GABAergic inhibition. ? 2013 Elsevier B.V.
机译:单萜酮,β-丁酮最初是苦艾的主要天然成分,引起人们的注意,并被怀疑对过量饮用这种饮料的人造成诸如幻觉和癫痫发作的不良影响。尽管随后的研究排除了β-thujone在绝对结合中的任何主要作用,但发现在高剂量下它可能诱导癫痫活性,表明与GABA能抑制作用相互作用。实际上,随后的研究,包括来自该实验室的研究表明,β-丁酮抑制了GABA能电流。但是,GABAA受体的异质性极高,在本研究中,我们研究了ε-硫j酮对不同重组GABAA受体的作用(ε1ε2ε2L,ε1ε2,ε1ε2,δ1ε2,δ1ε2,δ1ε2,δ1ε2,δ1ε2,δ1ε-1,δ1ε-1,δ1ε-1,δ1ε-1,δ1ε-1,δ1ε-1,δ1ε-1,δ1ε-1,δ1-ε-1,δ1-ε-1,δ1-ε-1,δ1-δ-1,δ1-ε-1,δ1-ε-1,δ1-ε-1,δ1-ε/α-1,δ-1-1。 2′和′4′2′′)与抑制的相态或补品形式有关。我们报道β-thujone通过定性相似的机制抑制所有被认为的受体类型,但是观察到最强的作用是β1-β2。受体,提示强直性电流可能比相性强。而且,我们证明,通过对培养的神经元中亚微摩尔GABA浓度(0.3ΔM)的响应进行模拟的补品电流,对γ-thujone的敏感性比由较高[GABA]引起的响应(与相电流相似)要大得多。 )或同一准备中的抑制性突触后电流。重要的是,β-thujone对强直电流的抑制程度与由α1-β2介导的电流一样强。受体。总而言之,这些数据提供了证据,表明不同的GABAA受体亚型对ε-丁酮表现出不同的敏感性,并表明该化合物可能会不同地影响GABA能抑制的补品和阶段性成分。 ? 2013 Elsevier B.V.

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