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正常肝脏与肝硬化肝脏对血管活性药物的不同反应。一项在离体灌注大鼠肝脏中的研究。

Differential response of normal and cirrhotic liver to vasoactive agents. A study in the isolated perfused rat liver.

作者信息

Ballet F, Chretien Y, Rey C, Poupon R

机构信息

Unité de Recherches d'Hépatologie, Institut National de la Santé et de la Recherche Médicale, Hôpital Saint-Antoine, Paris, France.

出版信息

J Pharmacol Exp Ther. 1988 Jan;244(1):283-9.

PMID:3336005
Abstract

In cirrhosis, endogenous vasoactive agents could act as modulators of intrahepatic resistance and thus portal pressure. The aim of this work was to study the effects of norepinephrine, angiotensin II and arg8-vasopressin on intrahepatic portal resistance in isolated perfused livers from normal rats and rats with carbon tetrachloride-induced cirrhosis. Livers were perfused at a constant pressure and the measured variable was portal blood flow. Dose-response curves were obtained by cumulative addition of agonists to the perfusate. The three vasoactive agents increased resistance in normal and cirrhotic livers. The maximal amplitude of response was similar in normal and cirrhotic livers. The cirrhotic livers exhibited an increased sensitivity to norepinephrine, a decreased sensitivity to angiotensin II but an unchanged sensitivity to arg8-vasopressin. The shape of the dose-response curve for norepinephrine and arg8-vasopressin, but not for angiotensin II, was modified in cirrhotic livers. We conclude that the cirrhotic liver retains a strong vascular reactivity to vasoactive agents and particularly to norepinephrine.

摘要

在肝硬化中,内源性血管活性物质可作为肝内阻力进而门静脉压力的调节因子。本研究旨在探讨去甲肾上腺素、血管紧张素II和精氨酸加压素对正常大鼠及四氯化碳诱导的肝硬化大鼠离体灌注肝脏肝内门静脉阻力的影响。肝脏在恒定压力下进行灌注,测量的变量为门静脉血流量。通过向灌注液中累积添加激动剂获得剂量-反应曲线。这三种血管活性物质均增加了正常肝脏和肝硬化肝脏的阻力。正常肝脏和肝硬化肝脏的最大反应幅度相似。肝硬化肝脏对去甲肾上腺素的敏感性增加,对血管紧张素II的敏感性降低,但对精氨酸加压素的敏感性无变化。在肝硬化肝脏中,去甲肾上腺素和精氨酸加压素的剂量-反应曲线形状发生改变,而血管紧张素II的未改变。我们得出结论,肝硬化肝脏对血管活性物质,尤其是去甲肾上腺素,仍具有较强的血管反应性。

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