首页> 外文期刊>American Journal of Physiology >Neurosteroid modulation of benzodiazepine-sensitive GABAA tonic inhibition in supraoptic magnocellular neurons.
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Neurosteroid modulation of benzodiazepine-sensitive GABAA tonic inhibition in supraoptic magnocellular neurons.

机译:苯二氮卓敏敏性GABA抑制中富集甲型粒细胞神经元的神经激素调节。

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摘要

Interactions between neurosteroids and GABA receptors have attracted particular attention in the supraoptic nucleus (SON). Although GABA(A) receptors (GABA(A)R) mediate a sustained tonic inhibitory current (I(tonic)), as well as conventional phasic inhibitory postsynaptic currents (IPSCs, I(phasic)) in the SON, whether the steroid modulation on I(tonic) is present in SON magnocelluar neurosecretory cells (MNCs) is unknown. Here, we addressed this question and gained insights into the potential molecular configuration of GABA(A) receptors mediating I(tonic) and conferring its neurosteroids sensitivity in SON MNCs. 4,5,6,7-tetrahydroisoxazolo[5,4-c]-pyridin-3-ol (THIP) (1 muM), a relatively selective extrasynaptic GABA(A)R agonist, facilitated I(tonic) without affecting the main characteristics of IPSCs, while DS-2, a relatively selective modulator of GABA(A)R delta-subunits, caused minimal changes in I(tonic) of SON MNCs. l-655,708, a relatively selective GABA(A)R alpha(5)-subunit inverse agonist, blocked approximately 35% of the total I(tonic) both under basal and elevated ambient GABA concentration (3 muM). Facilitation of I(tonic) by benzodiazepines further supported the role of GABA(A)R gamma(2)-subunit in I(tonic) of SON MNCs. Quantitative RT-PCR analysis showed much lesser expression of GABA(A)R delta-subunit than the alpha(5) or gamma(2)-subunit in the SON. Allopregnanolone and 3alpha,5alpha-tetrahydrodeoxycorticosterone increased both I(tonic) and I(phasic) in SON MNCs, respectively, although more than 90% of the current increase was mediated by I(tonic) during the neurosteroid facilitation. Finally, l-655,708 attenuated the neurosteroid facilitation of I(tonic) but not of I(phasic). Altogether, our results suggest that I(tonic), mediated mainly by benzodiazepine-sensitive GABA(A)Rs containing alpha(5)-, beta-, and gamma(2)-, and to a lesser extent, delta-subunits, is a potential target of neurosteroid modulation in SON neurons.
机译:神经活体和GABA受体之间的相互作用在上升核(儿子)中引起了特别的注意。虽然GABA(A)受体(GABA(A)R)介导持续的滋补抑制电流(I(滋补)),以及儿子中的常规相位抑制突触突出电流(IPSC,I(阶段),无论是类固醇调制在I(滋补品)上存在于儿子Magnocelluar神经细胞(MNC)中未知。在这里,我们解决了这个问题并获得了介导I(滋补品)的GABA(A)受体的潜在分子配置并在儿子MNC中赋予其神经活体敏感性的潜在分子配置。 4,5,6,7-四羟基异恶唑[5,4-c] - 吡啶-3-醇(Thip)(1妈妈),相对选择的额外促进GABA(A)R激动剂,促进I(滋补品)而不影响主要IPSCS的特征,而DS-2,GABA(A)R Delta-亚基的相对选择性调节剂,导致儿子MNC的I(Tonic)的最小变化。 L-655,708,一种相对选择的GABA(A)Rα(5)-subUnit逆激动剂,在基础和升高的环境GABA浓度(3米)下,占总I(滋补品)的约35%。通过苯并二氮杂化动物的促进I(滋补品)进一步支持CABA(A)Rγ(2)-Subit在儿子MNC中的rγ(2)-subit的作用。定量RT-PCR分析显示出比儿子(5)或儿子中的α(5)或γ(2)-subinit的GABA(a)r Delta-亚基表达更小。亚丙唑酮和3Alpha,5Alpha-四氢氧基菌酮分别增加了儿子MNC的I(滋补化)和I(序号),尽管在神经加湿型便利化期间通过I(滋补)介导的90%以上的电流增加。最后,L-655,708减弱了I(滋补)的神经活体促进,但不是I(序号)。完全,我们的结果表明,I(滋补品),主要由苯二氮卓敏感的GABA(A)Rs含有α(5) - ,β-和γ(2) - 以及较小程度的Delta-亚基儿子神经元神经激素调制的潜在目标。

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