首页> 美国卫生研究院文献>Frontiers in Neural Circuits >Primate cerebellar granule cells exhibit a tonic GABAAR conductance that is not affected by alcohol: a possible cellular substrate of the low level of response phenotype
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Primate cerebellar granule cells exhibit a tonic GABAAR conductance that is not affected by alcohol: a possible cellular substrate of the low level of response phenotype

机译:灵长类小脑颗粒细胞表现出不受酒精影响的滋补GABAAR电导:可能是低反应表型的细胞底物

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摘要

In many rodent brain regions, alcohol increases vesicular release of GABA, resulting in an increase in the frequency of spontaneous inhibitory postsynaptic currents (sIPSCs) and the magnitude of tonic GABAA receptor (GABAAR) currents. A neglected issue in translating the rodent literature to humans is the possibility that phylogenetic differences alter the actions of alcohol. To address this issue we made voltage-clamp recordings from granule cells (GCs) in cerebellar slices from the non-human primate (NHP), Macaca fascicularis. We found that similar to Sprague Dawley rats (SDRs), NHP GCs exhibit a tonic conductance generated by α6δ subunit containing GABAARs, as evidenced by its blockade by the broad spectrum GABAAR antagonist, GABAzine (10 μM), inhibition by α6 selective antagonist, furosemide (100 μM), and enhancement by THDOC (10–20 nM) and THIP (500 nM). In contrast to SDR GCs, in most NHP GCs (~60%), application of EtOH (25–105 mM) did not increase sIPSC frequency or the tonic GABAAR current. In a minority of cells (~40%), EtOH did increase sIPSC frequency and the tonic current. The relative lack of response to EtOH was associated with reduced expression of neuronal nitric oxide synthase (nNOS), which we recently reported mediates EtOH-induced enhancement of vesicular GABA release in rats. The EtOH-induced increase in tonic GABAAR current was significantly smaller in NHPs than in SDRs, presumably due to less GABA release, because there were no obvious differences in the density of GABAARs or GABA transporters between SDR and NHP GCs. Thus, EtOH does not directly modulate α6δ subunit GABAARs in NHPs. Instead, EtOH enhanced GABAergic transmission is mediated by enhanced GABA release. Further, SDR GC responses to alcohol are only representative of a subpopulation of NHP GCs. This suggests that the impact of EtOH on NHP cerebellar physiology will be reduced compared to SDRs, and will likely have different computational and behavioral consequences.
机译:在许多啮齿动物的大脑区域,酒精会增加GABA的囊泡释放,导致自发抑制性突触后电流(sIPSC)的频率和强直性GABAA受体(GABAAR)电流的幅度增加。在将啮齿动物文献翻译成人类时,一个被忽视的问题是,系统发育差异会改变酒精的作用。为了解决这个问题,我们在非人灵长类动物(NHP)猕猴中小脑切片中的颗粒细胞(GC)中制作了电压钳记录。我们发现,与Sprague Dawley大鼠(SDR)相似,NHP GCs表现出由含GABAARs的α6δ亚基产生的强音电导,其被广谱GABAAR拮抗剂GABAzine(10μM)阻断,α6选择性拮抗剂,速尿抑制所证明(100μM),并通过THDOC(10–20 nM)和THIP(500 nM)进行增强。与SDR GC相比,在大多数NHP GC中(约60%),使用EtOH(25–105 mM)不会增加sIPSC频率或强直GABAAR电流。在少数细胞中(约40%),EtOH确实增加了sIPSC频率和强直电流。对EtOH反应的相对缺乏与神经元一氧化氮合酶(nNOS)的表达降低有关,我们最近报道了它介导EtOH诱导的大鼠水泡GABA释放增强。在NHP中,EtOH引起的强直GABAAR电流增加明显小于SDR,这可能是由于GABA释放减少,因为SDR和NHP GC之间GABAAR或GABA转运蛋白的密度没有明显差异。因此,EtOH不能直接调节NHP中的α6δ亚基GABAAR。相反,EtOH增强的GABA能传递由增强的GABA释放介导。此外,SDR GC对酒精的反应仅代表NHP GC的亚群。这表明与SDR相比,EtOH对NHP小脑生理的影响将减少,并且可能会产生不同的计算和行为后果。

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