Yu J, Liang K, Tian D, Wang T, Tang W, Zhang W, Liu M
Department of Gastroenterology, Tongji Hospital of Tongji Medical University, Wuhan 430030, China.
Zhonghua Gan Zang Bing Za Zhi. 2001 Dec;9(6):352-4.
To understand the implication of differences of nitric oxide synthase (NOS) expression and activity between splanchnic arterial and venous vessels in the pathogenesis of portal hypertension.
Cirrhosis was induced in 100 Wistar rats by subcutaneously administration of carbon tetrachloride. NOS localization, activity and gene expression in the mesenteric artery and the portal vein vessels of both cirrhotic and normal rats were investigated by immunohistochemistry, chemoluminescence and reverse transcription-polymerase chain reaction, respectively.
There was inducible NOS enzyme isoform in al1 layers of splanchnic vessels of cirrhotic rats, whereas endothelial NOS isoform largely in vascular endothelia. NOS activity and its mRNA expression all were significantly increased in cirrhotic rats when compared with normal rats (P<0.05 or 0.01).Moreover, the activities of general and constitutive NOS and the expression of endothelial NOS mRNA in cirrhotic rats were significantly higher in the mesenteric artery than in the portal vein (P<0.01).
Enhanced expression and activity of endothelial NOS enzyme isoform may be mainly responsible for increased NO production of splanchnic vessels in cirrhotic rats, and the differences of NOS expression and activity between the mesenteric artery and the portal vein vessels may be one of the pathogeneses of portal hypertension in which NO might be involved.
了解内脏动脉和静脉血管中一氧化氮合酶(NOS)表达及活性差异在门静脉高压发病机制中的意义。
通过皮下注射四氯化碳诱导100只Wistar大鼠发生肝硬化。分别采用免疫组织化学、化学发光法及逆转录聚合酶链反应,研究肝硬化大鼠和正常大鼠肠系膜动脉及门静脉血管中NOS的定位、活性及基因表达。
肝硬化大鼠内脏血管各层均有诱导型NOS酶亚型,而内皮型NOS亚型主要存在于血管内皮。与正常大鼠相比,肝硬化大鼠的NOS活性及其mRNA表达均显著增加(P<0.05或0.01)。此外,肝硬化大鼠肠系膜动脉中总NOS和组成型NOS的活性以及内皮型NOS mRNA的表达均显著高于门静脉(P<0.01)。
内皮型NOS酶亚型表达及活性增强可能是肝硬化大鼠内脏血管NO生成增加的主要原因,肠系膜动脉与门静脉血管中NOS表达及活性的差异可能是门静脉高压的发病机制之一,且NO可能参与其中。