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慢性肝病中的尾加压素II:对血管张力的体内作用

Urotensin II in chronic liver disease: in vivo effect on vascular tone.

作者信息

Kemp William, Roberts Stuart, Komesaroff Paul A, Zomer Ella, Krum Henry

机构信息

Department of Gastroenterology, Alfred Hospital, Melbourne, Australia.

出版信息

Scand J Gastroenterol. 2008 Jan;43(1):103-9. doi: 10.1080/00365520701580009.

Abstract

OBJECTIVE

Urotensin II (UII) is now recognized as the most potent human vasoconstrictor. Although its role in human pathophysiology is unknown, vasoactive mediators are known to be important in the pathogenesis of portal hypertension complicating chronic liver disease. The objective of this study was to investigate the role of UII in liver cirrhosis via examination of the in vivo effect of UII in this patient group.

MATERIAL AND METHODS

The vasoactive effects of UII were measured using Laser Doppler velocimetry on cirrhotic patients (n = 14) and age-matched healthy controls (n = 14) after UII administration by iontophoresis to the cutaneous microcirculation of the forearm.

RESULTS

In vivo administration of UII produced vasoconstriction of the cutaneous microcirculation in the cirrhotic group and vasodilatation in the controls, with values differing significantly at the two highest doses of UII: 10(-9) mol (p = 0.01) and 10(-7) mol (p = 0.004).

CONCLUSIONS

UII mediates vasoconstriction of the microcirculation of cirrhotics but not of controls. This suggests that UII has pathophysiological relevance in the portal hypertensive population through its vasoactive properties. Further studies of UII and UII-antagonists are warranted in this patient population.

摘要

目的

尾加压素II(UII)现已被公认为是最强效的人类血管收缩剂。尽管其在人类病理生理学中的作用尚不清楚,但已知血管活性介质在慢性肝病并发门静脉高压的发病机制中起重要作用。本研究的目的是通过检测UII对该患者群体的体内作用,探讨UII在肝硬化中的作用。

材料与方法

通过离子电渗法将UII应用于前臂皮肤微循环后,采用激光多普勒血流仪测量14例肝硬化患者和14例年龄匹配的健康对照者UII的血管活性作用。

结果

在体内给予UII后,肝硬化组皮肤微循环出现血管收缩,而对照组出现血管舒张,在UII的两个最高剂量(10^(-9) mol,p = 0.01;10^(-7) mol,p = 0.004)时,两组数值差异显著。

结论

UII介导肝硬化患者的微循环血管收缩,但不介导对照组的血管收缩。这表明UII通过其血管活性特性在门静脉高压人群中具有病理生理学相关性。有必要对该患者群体进一步研究UII及UII拮抗剂。

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