کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1923227 | 1048882 | 2013 | 6 صفحه PDF | دانلود رایگان |

Pathological accumulation of 27-carbon intermediates or end-products of cholesterol metabolism, named oxysterols, may contribute to the onset and especially to the development of major chronic diseases in which inflammation, but also oxidative damage and to a certain extent cell death, are hallmarks and primary mechanisms of progression. Indeed, certain oxysterols exercise strong pro-oxidant and pro-inflammatory effects at concentrations detectable in the lesions typical of atherosclerosis, neurodegenerative diseases, inflammatory bowel diseases, age-related macular degeneration, and other pathological conditions characterized by altered cholesterol uptake and/or metabolism.
Graphical AbstractAAAFigure optionsDownload as PowerPoint slideResearch highlights
► Oxysterols are 27-carbon-atom products of enzymatic or non-enzymatic oxidation of cholesterol.
► Oxidative stress is the major non-enzymatic source of oxysterols.
► Oxysterols may in turn amplify oxidative redox imbalance in cells and tissues.
► Pathological accumulation of oxysterols triggers and sustains inflammatory reactions.
► Oxysterol-mediated inflammation is a primary mechanism of progression in major chronic diseases.
Journal: Redox Biology - Volume 1, Issue 1, 2013, Pages 125–130