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核因子E2相关因子2/血红素加氧酶1对实验性肝硬化门静脉高压症内脏血流动力学的影响

Effects of Nuclear Factor-E2-related factor 2/Heme Oxygenase 1 on splanchnic hemodynamics in experimental cirrhosis with portal hypertension.

作者信息

Qin Jun, He Yue, Duan Ming, Luo Meng

机构信息

Department of General Surgery, Shanghai Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.

Department of General Surgery, Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.

出版信息

Microvasc Res. 2017 May;111:12-19. doi: 10.1016/j.mvr.2016.12.009. Epub 2016 Dec 23.

Abstract

OBJECTIVE

We explored the effects of Nuclear Factor-E2-related factor 2 (Nrf2) and Heme Oxygenase 1 (HO-1) on splanchnic hemodynamics in portal hypertensive rats.

METHODS

Experimental cirrhosis with portal hypertension was induced by intraperitoneal injection of carbon tetrachloride. The expression of proteins was examined by immunoblotting. Hemodynamic studies were performed by radioactive microspheres. The vascular perfusion system was used to measure the contractile response of mesentery arterioles in rats.

RESULTS

Nrf2 expression in the nucleus and HO-1 expression in cytoplasm was significantly enhanced in portal hypertensive rats. Portal pressure, as well as regional blood flow, increased significantly in portal hypertension and can be blocked by tin protoporphyrin IX. The expression of endogenous nitric oxide synthase and vascular endothelial growth factors increased significantly compared to normal rats, while HO-1 inhibition decreased the expression of these proteins significantly. The contractile response of mesenteric arteries decreased in portal hypertension, but can be partially recovered through tin protoporphyrin IX treatment.

CONCLUSIONS

The expression of Nrf2/HO-1 increased in mesenteric arteries of portal hypertensive rats, which was related to oxidative stress. HO-1was involved in increased portal pressure and anomaly splanchnic hemodynamics in portal hypertensive rats.

摘要

目的

我们探讨了核因子E2相关因子2(Nrf2)和血红素加氧酶1(HO-1)对门静脉高压大鼠内脏血流动力学的影响。

方法

通过腹腔注射四氯化碳诱导实验性肝硬化伴门静脉高压。采用免疫印迹法检测蛋白表达。用放射性微球进行血流动力学研究。使用血管灌注系统测量大鼠肠系膜小动脉的收缩反应。

结果

门静脉高压大鼠的细胞核中Nrf2表达及细胞质中HO-1表达显著增强。门静脉高压时门静脉压力以及局部血流量显著增加,且可被锡原卟啉IX阻断。与正常大鼠相比,内源性一氧化氮合酶和血管内皮生长因子的表达显著增加,而HO-1抑制则显著降低这些蛋白的表达。门静脉高压时肠系膜动脉的收缩反应降低,但通过锡原卟啉IX治疗可部分恢复。

结论

门静脉高压大鼠肠系膜动脉中Nrf2/HO-1表达增加,这与氧化应激有关。HO-1参与了门静脉高压大鼠门静脉压力升高和内脏血流动力学异常。

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