The role of autophagy and the intrahepatic vascular resistance in the pathophysiology of non-alcoholic fatty liver disease (NAFLD).
Abstract
In our study we focus on disturbances in the liver blood flow. Previously we showed that severe steatosis leads to a significant rise in blood pressure in the portal system ("portal hypertension") preceding the occurrence of inflammation. The degree of portal hypertension appeared to be related to the severity of steatosis. These findings points towards a significant increase in intrahepatic resistance and subsequent impairment of liver blood flow. The intrahepatic resistance has, however, to date never been directly investigated in NAFLD. In the current study we will therefore focus on the intrahepatic resistance and its (functional and morphological) determinants in a rat model of severe steatosis. Potential contribution of different cell types (Kupffer cells, stellate cells) and of different mediators to intrahepatic vascular tone (e.g. Nitric Oxid) will be examined in detail.Researcher(s)
- Promoter: Michielsen Peter
- Co-promoter: Francque Sven
- Fellow: Kwanten Wilhelmus
Research team(s)
Project type(s)
- Research Project
Study of the intrahepatic resistance and its determinants in a rat model of severe non-alcoholic fatty liver disease (NAFLD).
Abstract
In our study we focus on disturbances in the liver blood flow. Previously we showed that severe steatosis leads to a significant rise in blood pressure in the portal system ("portal hypertension") preceding the occurrence of inflammation. The degree of portal hypertension appeared to be related to the severity of steatosis. These findings points towards a significant increase in intrahepatic resistance and subsequent impairment of liver blood flow. The intrahepatic resistance has, however, to date never been directly investigated in NAFLD. In the current study we will therefore focus on the intrahepatic resistance and its (functional and morphological) determinants in a rat model of severe steatosis. Potential contribution of different cell types (Kupffer cells, stellate cells) and of different mediators to intrahepatic vascular tone (e.g. Nitric Oxid) will be examined in detail.Researcher(s)
- Promoter: Michielsen Peter
- Co-promoter: Francque Sven
- Co-promoter: Pelckmans Paul
- Fellow: Kwanten Wilhelmus
Research team(s)
Project type(s)
- Research Project
Mechanisms of portal hypertension.
Abstract
This project represents a formal research agreement between UA and on the other hand UZA. UA provides UZA research results mentioned in the title of the project under the conditions as stipulated in this contract.Researcher(s)
- Promoter: Michielsen Peter
Research team(s)
Project type(s)
- Research Project