Primary sclerosing cholangitis (PSC) is a cholestatic (cholestasis = "stagnation of bile") liver disease characterised by chronic inflammation and progressive scarring of the bile ducts. Up to 80 percent of PSC patients simultaneously suffer from chronic inflammatory bowel disease, especially ulcerative colitis. This disease has been suggested to promote the development and progression of PSC. Since there are no effective drugs that improve the course of PSC, many patients develop cirrhosis of the liver - in which case liver transplantation remains the last therapeutic option.
The results of the now published study show that a local inflammation of the intestine, which is triggered by the molecule dextran sulphate (DSS), induces major changes in the signalling pathways of the liver. Thus, the teams from Dortmund and Aachen were able to detect an upregulation of the inflammatory pathways and, surprisingly, a suppression of bile acid synthesis and transport. The study identifies a molecular regulatory circuit by which inflammation of the intestine reduces the production if bile and thus suppresses the progression of the cholestatic liver disease.
The discovered molecular mechanism may be used in the future to slow down the production of bile acids when the liver cells are already overloaded with these substances. The contribution of the IfADo team consisted of a special functional imaging technique with which the concentrations of bile acids and other metabolites in the tissue can be visualized and analysed.
The liver is the largest organ of the human body and is responsible for more than 500 specific functions in the organism, for example the detoxification of toxic substances. Diseases of the liver also have a negative impact on cells and other organs, especially the brain, kidney and immune functions. The liver also works closely with the intestines. It releases messenger substances into the intestine via the bile and conversely also receives signals from the intestine via the blood of the portal vein.
MEDICA-tradefair.com; Source: Leibniz-Institut für Arbeitsforschung an der TU Dortmund
