Minuk G Y, MacCannell K L
Department of Medicine, University of Calgary, Alberta, Canada.
Hepatology. 1988 Jan-Feb;8(1):73-7. doi: 10.1002/hep.1840080115.
Systolic and diastolic blood pressures were recorded in 176 ambulant patients with chronic liver disease, including 36 patients with compensated cirrhosis (Group I), 119 patients with noncirrhotic chronic liver disease (Group II) and 21 patients with benign structural or functional liver disease (Group III). Group I patients had significantly lower systolic (113.0 +/- 2.2 mm Hg, mean +/- S.E.) and diastolic (65.3 +/- 1.7 mm Hg) pressures than Group II patients (125.8 +/- 3.5 and 76.6 +/- 1.5 mm Hg, respectively (p less than 0.0001) or Group III patients (125.1 +/- 3.4 and 77.5 +/- 2.4 mm Hg, respectively) (p less than 0.0001). Serum levels of GABA, a potent amino acid neurotransmitter with known vasodilatory effects in vitro, were higher in Group I patients (1.12 +/- 0.26 microM, mean +/- S.E.) than in Group II patients (0.41 +/- 0.05 microM) (p less than 0.005) or Group III patients (0.34 +/- 0.03 mM) (p less than 0.05). A constant infusion of GABA into the systemic circulation of six adult dogs, at rates required to achieve serum GABA levels within one order of magnitude of those observed in humans with cirrhosis, resulted in a 17.0 +/- 4.3 mm Hg decrease in systolic pressure (p less than 0.05) and a 10.8 +/- 3.7 mm Hg decrease in diastolic pressure (p less than 0.05). Control amino acids were not vasoactive. The results of this study suggest that, in addition to other vasoactive compounds, a GABA-mediated process might contribute to the hypotension observed in patients with compensated cirrhosis.
对176例慢性肝病门诊患者记录了收缩压和舒张压,其中包括36例代偿期肝硬化患者(I组)、119例非肝硬化慢性肝病患者(II组)和21例良性肝脏结构或功能疾病患者(III组)。I组患者的收缩压(113.0±2.2 mmHg,均值±标准误)和舒张压(65.3±1.7 mmHg)显著低于II组患者(分别为125.8±3.5和76.6±1.5 mmHg)(p<0.0001)或III组患者(分别为125.1±3.4和77.5±2.4 mmHg)(p<0.0001)。血清γ-氨基丁酸(GABA)水平在I组患者中(1.12±0.26 μM,均值±标准误)高于II组患者(0.41±0.05 μM)(p<0.005)或III组患者(0.34±0.03 mM)(p<0.05),GABA是一种在体外具有已知血管舒张作用的强效氨基酸神经递质。以在肝硬化患者中观察到的血清GABA水平的一个数量级范围内所需的速率,对6只成年犬进行GABA持续输注入体循环,导致收缩压下降17.0±4.3 mmHg(p<0.05),舒张压下降10.8±3.7 mmHg(p<0.05)。对照氨基酸无血管活性。本研究结果表明,除其他血管活性化合物外,GABA介导的过程可能导致代偿期肝硬化患者出现低血压。