| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5513718 | Microvascular Research | 2017 | 8 Pages |
â¢Enhanced Nrf2 and HO-1 expression in portal hypertensive rats has been demonstrated.â¢HO-1 is involved in increased portal pressure and anomaly splanchnic hemodynamicsâ¢HO-1 led to increased VEGF expression in portal hypertensive rats.â¢Nrf2 and HO-1 have the potential to be a therapeutic target in portal hypertension.
ObjectiveWe explored the effects of Nuclear Factor-E2-related factor 2 (Nrf2) and Heme Oxygenase 1 (HO-1) on splanchnic hemodynamics in portal hypertensive rats.MethodsExperimental 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.ResultsNrf2 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.ConclusionsThe 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.
