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血管紧张素II在早期和晚期肝硬化中对基础血管张力及交感神经刺激引起的血管张力调节中的作用

Role of angiotensin II in regulation of basal and sympathetically stimulated vascular tone in early and advanced cirrhosis.

作者信息

Helmy A, Jalan R, Newby D E, Hayes P C, Webb D J

机构信息

Liver Unit, Department of Medicine, Royal Infirmary of Edinburgh, Edinburgh, Scotland.

出版信息

Gastroenterology. 2000 Mar;118(3):565-72. doi: 10.1016/s0016-5085(00)70263-0.

Abstract

BACKGROUND & AIMS: The renin-angiotensin and sympathetic nervous systems are activated in cirrhosis. This study aimed to establish the role of angiotensin II (ANG II) in the regulation of basal and sympathetically stimulated vascular tone in preascitic cirrhotic patients and patients with diuretic-refractory ascites compared with age- and sex-matched healthy controls.

METHODS

Forearm blood flow (FBF) responses to lower body negative pressure (LBNP) and to subsystemic, intrabrachial infusions of losartan, an angiotensin II type 1 (AT(1)) receptor antagonist, norepinephrine, and ANG II were measured using venous occlusion plethysmography.

RESULTS

In all groups, ANG II and norepinephrine caused dose-dependent reductions in FBF (P < 0.001); responses to norepinephrine were similar across the 3 groups but those to ANG II were less in both cirrhotic groups than in controls (P < 0.01). Losartan caused a dose-dependent increase in FBF only in patients with refractory ascites (P < 0.01). LBNP caused less reduction in FBF in refractory ascites patients than in both preascitic patients and controls (P < 0.01).

CONCLUSIONS

Despite hyporesponsiveness to exogenous ANG II in both early and advanced cirrhosis, endogenous ANG II contributes to the maintenance of basal vascular tone only in advanced cirrhosis. These findings suggest a role of ANG II in the pathogenesis of ascites. Attenuated LBNP responses occurred only in advanced cirrhosis, without apparent interaction with endogenous ANG II.

摘要

背景与目的

肾素 - 血管紧张素系统和交感神经系统在肝硬化患者中被激活。本研究旨在确定与年龄和性别匹配的健康对照相比,血管紧张素II(ANG II)在腹水前期肝硬化患者和利尿剂抵抗性腹水患者基础血管张力及交感神经刺激血管张力调节中的作用。

方法

采用静脉阻断体积描记法测量前臂血流量(FBF)对下体负压(LBNP)以及对肱动脉内输注血管紧张素II 1型(AT(1))受体拮抗剂氯沙坦、去甲肾上腺素和ANG II的反应。

结果

在所有组中,ANG II和去甲肾上腺素均导致FBF呈剂量依赖性降低(P < 0.001);三组对去甲肾上腺素的反应相似,但肝硬化两组对ANG II的反应均低于对照组(P < 0.01)。氯沙坦仅在难治性腹水患者中导致FBF呈剂量依赖性增加(P < 0.01)。LBNP导致难治性腹水患者的FBF降低幅度小于腹水前期患者和对照组(P < 0.01)。

结论

尽管早期和晚期肝硬化对外源性ANG II反应低下,但内源性ANG II仅在晚期肝硬化中有助于维持基础血管张力。这些发现提示ANG II在腹水发病机制中起作用。LBNP反应减弱仅发生在晚期肝硬化,且与内源性ANG II无明显相互作用。

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