Hernández-Avila C A, Shoemaker W J, Ortega-Soto H A
Department of Psychiatry, University of Connecticut Health Center, Farmington 06030, USA.
J Psychiatry Neurosci. 1998 Sep;23(4):217-22.
Hepatic encephalopathy (HE) is a complex neuropsychiatric disorder secondary to acute or chronic liver failure. Although the exact causes of HE have not been clarified, enhanced central nervous system inhibition at the gamma-aminobutyric acid (GABA)-benzodiazepine receptor complex, mediated by increased levels of endogenous benzodiazepine-receptor ligands (BZRL), has been proposed. Research exploring this hypothesis has yielded contradictory findings. This study evaluated the presence and levels of BZRL in plasma from patients with HE and 3 comparison groups.
Cross-sectional study.
Twenty-four patients with HE, 10 patients with liver cirrhosis without encephalopathy (LC), 4 patients with uremic encephalopathy (UE), and 9 healthy subjects.
Radio-receptor assay of plasma samples from patients and controls.
Plasma levels of BZRL.
The patients in the HE group had significantly higher plasma BZRL levels than the patients with UE and the healthy subjects, but not than those with LC, in whom these compounds were also detected in significant concentrations. When patients were classified according to the severity of HE, plasma of BZRL showed a modest correlation with stage of severity (r = 0.37). Interestingly, approximately one-third of the patients with HE did not have detectable levels of BZRL.
Endogenous BZRL may play a role in the pathogenesis of HE, although neuropsychiatric symptoms in HE are difficult to explain in terms of these compounds alone.
肝性脑病(HE)是继发于急性或慢性肝衰竭的一种复杂的神经精神障碍。尽管HE的确切病因尚未阐明,但有人提出,内源性苯二氮䓬受体配体(BZRL)水平升高介导的γ-氨基丁酸(GABA)-苯二氮䓬受体复合物处中枢神经系统抑制作用增强。探索这一假说的研究得出了相互矛盾的结果。本研究评估了HE患者以及3个对照组血浆中BZRL的存在情况和水平。
横断面研究。
24例HE患者、10例无脑病的肝硬化(LC)患者、4例尿毒症脑病(UE)患者和9名健康受试者。
对患者和对照组的血浆样本进行放射受体分析。
血浆BZRL水平。
HE组患者的血浆BZRL水平显著高于UE患者和健康受试者,但不高于LC患者,LC患者血浆中也检测到了高浓度的这些化合物。根据HE的严重程度对患者进行分类时,BZRL血浆水平与严重程度分期呈中度相关(r = 0.37)。有趣的是,约三分之一的HE患者检测不到BZRL水平。
内源性BZRL可能在HE的发病机制中起作用,尽管仅用这些化合物难以解释HE的神经精神症状。