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肝昏迷患者大脑中 DHEAS 水平降低:肝性脑病中 GABA 能紧张度增加的意义。

Reduced brain levels of DHEAS in hepatic coma patients: significance for increased GABAergic tone in hepatic encephalopathy.

机构信息

Polydisciplinary Faculty of Khouribga, Hassan I University, Khouribga, Morocco.

出版信息

Neurochem Int. 2012 Jul;61(1):48-53. doi: 10.1016/j.neuint.2012.03.020. Epub 2012 Apr 3.

Abstract

Increased neurosteroids with allosteric modulatory activity on GABA(A) receptors such as 3α-5α tertrahydroprogesterone; allopregnanolone (ALLO), are candidates to explain the phenomenon of "increased GABAergic tone" in hepatic encephalopathy (HE). However, it is not known how changes of other GABA(A) receptor modulators such as dehydroepiandrosterone sulfate (DHEAS) contribute to altered GABAergic tone in HE. Concentrations of DHEAS were measured by radioimmunoassay in frontal cortex samples obtained at autopsy from 11 cirrhotic patients who died in hepatic coma and from an equal number of controls matched for age, gender, and autopsy delay intervals free from hepatic or neurological diseases. To assess whether reduced brain DHEAS contributes to increased GABAergic tone, in vitro patch clamp recordings in rat prefrontal cortex neurons were performed. A significant reduction of DHEAS (5.81±0.88 ng/g tissue) compared to control values (9.70±0.79 ng/g, p<0.01) was found. Brain levels of DHEAS in patients with liver disease who died without HE (11.43±1.74 ng/g tissue), and in a patient who died in uremic coma (12.56 ng/g tissue) were within the control range. Increasing ALLO enhances GABAergic tonic currents concentration-dependently, but increasing DHEAS reduces these currents. High concentrations of DHEAS (50 μM) reduce GABAergic tonic currents in the presence of ALLO, whereas reduced concentrations of DHEAS (1 μM) further stimulate these currents. These findings demonstrate that decreased concentrations of DHEAS together with increased brain concentrations of ALLO increase GABAergic tonic currents synergistically; suggesting that reduced brain DHEAS could further increase GABAergic tone in human HE.

摘要

在肝性脑病(HE)中,具有变构调节 GABA(A) 受体(如 3α-5α 四氢孕酮;别孕烯醇酮(ALLO))活性的神经甾体增加,被认为是“增加 GABA 能张力”现象的候选解释。然而,其他 GABA(A) 受体调节剂(如脱氢表雄酮硫酸酯(DHEAS))的变化如何导致 HE 中 GABA 能张力的改变尚不清楚。通过放射免疫测定法测量 11 例死于肝性昏迷的肝硬化患者和 11 例年龄、性别和尸检延迟时间相匹配的无肝或神经疾病的对照者死后尸检获得的额皮质样本中的 DHEAS 浓度。为了评估脑内 DHEAS 减少是否导致 GABA 能张力增加,在大鼠前额皮质神经元中进行了体外膜片钳记录。与对照组(9.70±0.79ng/g,p<0.01)相比,患者脑组织中的 DHEAS 水平显著降低(5.81±0.88ng/g)。未发生 HE 的肝病患者(11.43±1.74ng/g 组织)和死于尿毒症昏迷的患者(12.56ng/g 组织)的脑内 DHEAS 水平在正常范围内。增加 ALLO 浓度依赖性地增强 GABA 能紧张性电流,但增加 DHEAS 会降低这些电流。高浓度的 DHEAS(50μM)在 ALLO 存在下降低 GABA 能紧张性电流,而低浓度的 DHEAS(1μM)则进一步刺激这些电流。这些发现表明,DHEAS 浓度降低与脑内 ALLO 浓度增加协同增加 GABA 能紧张性电流;提示脑内 DHEAS 减少可能进一步增加人类 HE 中的 GABA 能张力。

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