Bile acids: Regulation of apoptosis by ursodeoxycholic acid

Joana D. Amaral, Ricardo J.S. Viana, Rita M. Ramalho, Clifford J. Steer, Cecilia M.P. Rodrigues

Research output: Contribution to journalReview articlepeer-review

288 Scopus citations

Abstract

Bile acids are a group of molecular species of acidic steroids with peculiar physical-chemical and biological characteristics. At high concentrations they become toxic to mammalian cells, and their presence is pertinent in the pathogenesis of several liver diseases and colon cancer. Bile acid cytoxicity has been related to membrane damage, but also to nondetergent effects, such as oxidative stress and apoptosis. Strikingly, hydrophilic ursodeoxycholic acid (UDCA), and its taurine-conjugated form (TUDCA), show profound cytoprotective properties. Indeed, these molecules have been described as potent inhibitors of classic pathways of apoptosis, although their precise mode of action remains to be clarified. UDCA, originally used for cholesterol gallstone dissolution, is currently considered the first choice therapy for several forms of cholestatic syndromes. However, the beneficial effects of both UDCA and TUDCA have been tested in other experimental pathological conditions with deregulated levels of apoptosis, including neurological disorders, such as Alzheimer's, Parkinson's, and Huntington's diseases. Here, we review the role of bile acids in modulating the apoptosis process, emphasizing the anti-apoptotic effects of UDCA and TUDCA, as well as their potential use as novel and alternate therapeutic agents for the treatment of apoptosis-related diseases.

Original languageEnglish (US)
Pages (from-to)1721-1734
Number of pages14
JournalJournal of lipid research
Volume50
Issue number9
DOIs
StatePublished - 2009

Keywords

  • Bcl-2 family
  • Cell death
  • Liver
  • Neuroprotection
  • Nuclear steroid receptors

Fingerprint

Dive into the research topics of 'Bile acids: Regulation of apoptosis by ursodeoxycholic acid'. Together they form a unique fingerprint.

Cite this