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Oxysterol

From Wikipedia, the free encyclopedia

An oxysterol is a derivative of cholesterol obtained by oxidation involving enzymes and / or pro-oxidants. Such compounds play important roles in various biological processes such as cholesterol homeostasis, lipid metabolism (sphingolipids, fatty acids), apoptosis, autophagy, and prenylation of proteins; the mode of action of oxysterols in these effects is still poorly understood. Several oxysterols are associated with age-related diseases such as cardiovascular disease, eye disease (cataract, age-related macular degeneration), certain neurodegenerative diseases and cancers.[1] The activities of oxysterols in these diseases could be due to their pro-oxidative and pro-inflammatory activities and their ability to act on cellular organelles (mitochondria, peroxisome, lysosome) that can contribute to activate apoptosis and autophagy. There are arguments supporting that oxysterols have important roles in atherosclerosis progression which is involved in several cardiovascular diseases.[2][3][4]

Identifying therapies to regulate the body's production of oxysterols and their biological activities is of therapeutic interest.

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References

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  1. ^ Samadi, A (Jan 2021). "A Comprehensive Review on Oxysterols and Related Diseases". Current Medicinal Chemistry. 28 (1): 110–136. doi:10.2174/0929867327666200316142659. PMID 32175830. S2CID 212729018.
  2. ^ Schroepfer, Gj Jr (Jan 2000). "Oxysterols: modulators of cholesterol metabolism and other processes" (Free full text). Physiological Reviews. 80 (1): 361–554. doi:10.1152/physrev.2000.80.1.361. ISSN 0031-9333. PMID 10617772.
  3. ^ Björkhem, I (Sep 2002). "Do oxysterols control cholesterol homeostasis?". The Journal of Clinical Investigation. 110 (6): 725–30. doi:10.1172/JCI16388. PMC 151135. PMID 12235099.
  4. ^ Ingemar Björkhem; Ulf Diczfalusy (2002). "Oxysterols: Friends, Foes, or Just Fellow Passengers?". Arteriosclerosis, Thrombosis, and Vascular Biology. 22 (5): 734–42. doi:10.1161/01.ATV.0000013312.32196.49. PMID 12006384.