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Inflammation: Cause or consequence of chronic cholestatic liver injury.
Woolbright, Benjamin L.
Affiliation
  • Woolbright BL; Department of Urology, University of Kansas Medical Center, Kansas City, KS, USA. Electronic address: bwoolbright@kumc.edu.
Food Chem Toxicol ; 137: 111133, 2020 Mar.
Article in En | MEDLINE | ID: mdl-31972189
ABSTRACT
Cholestasis is a result of obstruction of the biliary tracts. It is a common cause of liver pathology after exposure to toxic xenobiotics and during numerous other liver diseases. Accumulation of bile acids in the liver is thought to be a major driver of liver injury during cholestasis and can lead to eventual liver fibrosis and cirrhosis. As such, current therapy in the field of chronic liver diseases with prominent cholestasis relies heavily on increasing choleresis to limit accumulation of bile acids. Many of these same diseases also present with autoimmunity before the onset of cholestasis though, indicating the inflammation may be an initiating component of the pathology. Moreover, cytotoxic inflammatory mediators accumulate during cholestasis and can propagate liver injury. Anti-inflammatory biologics and small molecules have largely failed clinical trials in these diseases though and as such, targeting inflammation as a means to address cholestatic liver injury remains debatable. The purpose of this review is to understand the different roles that inflammation can play during cholestatic liver injury and attempt to define how new therapeutic targets that limit or control inflammation may be beneficial for patients with chronic cholestatic liver disease.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cholestasis Type of study: Etiology_studies Limits: Animals / Humans Language: En Journal: Food Chem Toxicol Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cholestasis Type of study: Etiology_studies Limits: Animals / Humans Language: En Journal: Food Chem Toxicol Year: 2020 Document type: Article
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