Molecular Medicine Reports · 2017 · 12 citations · 17 references
Life SciencesBiochemistryPharmacologyHepatotoxicologyRedox BiochemistryTranscriptional RegulationHeme MetabolismHepatic FibrosisHepatic PathophysiologyHepatotoxicity MechanismsLiver DiseaseLiver PhysiologyActivated Hepatic Stellate CellsAntioxidant PropertiesBilirubin MetabolismHeme DegradationHepatic Stellate Cell BiologyHepatic Stellate Cell FunctionLiver Fibrosis ProgressionReactive Oxygen Species Injury
Hepatic stellate cell (HSC) activation serves a key role in liver fibrosis, and is associated with chronic liver diseases. Bilirubin, a product of heme degradation, has been demonstrated to have antioxidant properties. The present study investigated the effects of physiological concentrations of bilirubin on rat HSC activation. Rat HSCs were isolated and cultured for several generations to induce activation. The activated HSCs were subsequently treated with 0, 1, 10 or 20 mg/l bilirubin and assayed for parameters of cell activation. As the bilirubin concentration increased, HSCs demonstrated reduced production of reactive oxygen species, reduced protein expression levels of α‑smooth muscle actin, a decreased mRNA expression ratio of tissue inhibitor of matrix metalloproteinase‑1/matrix metalloproteinase‑2, decreased proliferation and increased apoptosis. In conclusion, elevated bilirubin levels, within its physiological concentration range, appeared to inhibit HSC activation. These findings suggested a potential role for bilirubin in the treatment of fibrosis that requires further investigation.
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Bilirubin Is an Antioxidant of Possible Physiological Importance
Roland Stocker, Yorihiro Yamamoto, Antony F. McDonagh et al. · Science · 1987 · 3.5K citations
NO Modulates NADPH Oxidase Function Via Heme Oxygenase-1 in Human Endothelial Cells
Fan Jiang, Sarah J. Roberts, Srinivasa Raju Datla et al. · Hypertension · 2006 · 158 citations · Full text